Skip to main content
NCBI home page
OncoTargets and Therapy logoLink to OncoTargets and Therapy
. 2020 Sep 28;13:9611–9622. doi: 10.2147/OTT.S266541

Role of miRNA-424 in Cancers

Shulin Li 1, Yuqi Wu 1, Jiawei Zhang 1, Hao Sun 2, Xiangwei Wang 1,✉
PMCID: PMC7532073  PMID: 33061443

Abstract

microRNA (miRNA) is an important part of non-coding RNA that regulates gene expression at a posttranscriptional level. miRNA has gained increasing interest in recent years, both in research and clinical fields. miRNAs have been found to play an important role in various diseases, particularly cancer. Aberrant miR-424 expression is found in several tumors where they can function as either oncogenes or tumor-suppressor genes. Meanwhile, miR-424 is also affected by the reorganization of many other non-coding RNAs such as lncRNA and cirRNA. Several studies have found that miR-424 participates in proliferation, differentiation, apoptosis, invasion, angiogenesis, and drug resistance, and plays an important role in the tumorigenesis and progression of tumors. This review will focus on the recent progress of research on miR-424 in tumors.

Keywords: miRNAs, miR-424, tumor, regulation, carcinogenesis, cancer progression

Introduction

MicroRNA (miRNA) has been the subject of many studies since its discovery in 1993.1 miRNA is an important class of non-coding RNA that function as post-transcriptional regulators of gene expression in cells by repressing and fine-tuning protein output. Although miRNA accounts for only 1% of the human genome, it regulates one-third of the gene expression in humans.2–4 miRNAs are ubiquitous in eukaryotes, and are highly conservative, time-series, and tissue-cell specific. miRNAs are composed of a large group of non-coding small RNAs (approximately 21–23nt).5 miRNA formation comprises three main steps: transcription, maturation, and functional complex assembly. The gene encoding miRNA in the nucleus is first transcribed under the catalysis of RNA polymerase II to form a primary transcript with a cap structure (5MGpppG) and a poly-A tail (PolyA) of several hundred nucleotides in length.6 The primary transcript is further processed into a single precursor pre-miRNA, with a stem-loop structure containing only 70–100 nt under the action of the RNase family enzyme Drosha. The pre-miRNA is then transported to the cytoplasm by HASTY (HST), a homolog of the export protein Exportin-5.7–9 In conjunction with the RNaseIII family enzyme Dicer, the pre-miRNA is processed to form double-stranded miRNA, which subsequently forms double strand mature miRNA.10 Mature miRNAs combine with a ribonucleoprotein complex similar to RISC (RNA-induced silencing complex) to form miRNP, which recognizes target genes.9,11 After miRNA is loaded into the RISC complex, it functions in the regulation of gene expression. miRNA recognizes binding sites on the mRNA 3ʹUTR through its seed sequence (nucleotides 2–8 at the 5 ‘end), carries RISC, and inhibits protein expression. The three main functions of miRNA are transcriptional repression, and mRNA cleavage or degradation.12–14 Existing studies have found that approximately 30% of human protein expression is regulated by miRNAs.15 By interacting with the 3ʹUTR, miRNA can simultaneously regulate the expression of many genes, thereby regulating signaling pathways at multiple levels.16,17

Evidence increasingly suggests that miR-424 plays an important role in different types of diseases, including sperm damage,18 psoriasis,19 amyotrophic lateral sclerosis (ALS),20 insulin resistance,21 and acute respiratory distress syndrome (ARDS).22 However, the research on miR-424 is more abundant in cases of tumors involving early diagnosis, development, treatment, prognosis. This review focuses on the role of miR-424 in tumor progression.

Dual Regulatory Function of miRNA-424

The expression level of miR-424 in tumors can be either high or low, highlighting its multiple roles. Due to differences in expression, it is possible to diagnose disease and predict prognosis by detecting the amount of miRNA-424 in the blood or other body fluids.

Multilateral statistical evaluations have repeatedly confirmed the combination of highly specific biomarkers composed of four urine microRNAs (miR-424, miR-423, miR-660, and let7-i) as indicators to distinguish breast cancer patients from healthy controls, with sensitivity of 98.6% and specificity of 100%. This is of great significance for the non-invasive auxiliary diagnosis of breast cancer.23 Meanwhile, currently basing on the PSA to diagnosis prostate cancer is limited. A previous study identified that a low expression level of miR-424-3p was associated with the invasive phenotype and recurrence of prostate cancer.24,25 It can be detected by miR-424 combined with PSA value and prostate volume to assist in the diagnosis of prostate cancer in patients with elevated PSA.26

In addition to studies on endocrine organs, the association between miRNAs and digestive system tumors has also been explored. The overall survival rate of pancreatic adenocarcinoma (PAAD) is associated with miRNAs including miR-424, which may have the potential to become a prognostic biomarker for PAAD.27 Several studies have found that miR-424-5p is a tumor suppressor miRNA in hepatocellular carcinoma (HCC), and miR-424-5p is closely related to cell proliferation and invasion.28–30 Furthermore, it has been shown that miR-424 can predict the recurrence of liver cancer after liver transplantation, and that low expression of miR-424 is an independent prognostic factor of relapse, primarily through promoting the migration, invasion, and proliferation of HCC cells.31 In the respiratory system, it has been shown that high expression of miR-424 indicates a worse prognosis for patients with non-small cell lung cancer.32

In summary, a large number of studies have found that the expression level of miRNA-424 in different tumors has significance in the diagnosis and prognosis of tumors.

Function of miR-424 and Roles in Tumor Progression

MicroRNA regulates gene expression at the post-transcription level and is involved in regulating several key processes including cell proliferation, apoptosis, stem cell differentiation, invasion and metastasis, and other physiological and pathological processes. As mentioned above, the expression of miR-424 in tumors is closely related to the occurrence and development of disease. At the same time, a large number of studies have found that by changing the expression of miR-424 in tumors to regulate different target genes, cell function can also be altered.

Multiplication, Invasion, and Migration

Tumor proliferation, invasion and migration are complex processes with multiple factors and steps that involve oncogenes, tumor suppressor genes, signal transduction genes, and numerous cytokines and regulatory factors. Studies have found that miRNAs play different functions in different diseases. For instance, in the nervous system, glioma is one of the most deadly malignant tumors, in which miR-424 plays a role in suppressing cancer in glioma cells and is down-regulated by DNA methylation.33 Further research found that miR-424 can inhibit cell migration and epithelial-mesenchymal transition (EMT) by targeting KIF23 in glioma.34 Moreover, in the reproductive system, based on the exact relationship between HPV infection and cervical cancer, studies have found that in HPV (+) cervical cancer cells, CHK1 and Wee1, the two targets of miR-424, are suppressed. These factors have important roles in DNA damage repair,35 and further research found that regulating CHK1 can affect cervical cancer cell migration and invasion, apoptosis, and cell cycle changes. Furthermore, miR424-5p can target KDM5B through the Notch signaling pathway to influence cervical cancer cell proliferation.36,37 In endometrial cancer, miR-424 can inhibit cell proliferation by targeting E2F7, increase cell apoptosis, and cause cell cycle arrest38 Another study found that miR-424 can inhibit cell invasion and sphere formation by inhibiting MMSET, as well as inhibiting cell migration, invasion, and EMT by downregulating doublecortin-like kinase 1 (DCLK1). miR-424 can also target G protein-coupled estrogen receptor −1 (GPER-1), which in turn affects the PI3K/AKT signaling pathway to regulate cell proliferation.39–42

In summary, a large number of studies on the female reproductive system have indicated that miR-424 is involved in regulating the malignant biological behavior of tumors by regulating the expression of target genes, which may become an important marker for tumor diagnosis and prognosis, and may even have potential as an anti-tumor adjuvant therapy.

In nasopharyngeal carcinoma, miR-424-5p acts an oncogene that promotes the aggressive progression of laryngosquamous cell carcinoma (LSCC), and a high miR-424-5p level is significantly associated with poor differentiation, advanced tumors, and cervical lymph node metastasis.43 In oral squamous cell carcinoma, it has been found that miR-424-5p is involved in cell migration and invasion by negatively regulating the expression of SOCS2.44 Meanwhile, studies in a variety of digestive system tumors have found that miR-424 can either promote or suppress cancer. miR-424-5p is a carcinogen in colorectal cancer (CRC) that directly promotes proliferation and metastasis by targeting SCN4B, CCNE1, AKT3, and Rictor.45–48 In the field of hepatobiliary carcinoma, it has been found that miR-424-5p can inhibit the metastasis and invasion of intrahepatic cholangiocarcinoma by targeting ARK5. Moreover, in liver cancer, miR-424 can inhibit the proliferation and invasion of tumors by targeting TRIM29, YAP1, and c-Myb, while miR-424-5p can also target ICAT and inhibit tumor progression by reversing the EMT process of primary liver cancer.28,49–52 Another group has found that miR-424 inhibits tumor growth by inhibiting the Akt3/E2F3 axis in liver cancer tissues.53 Other studies have found that in hepatoma cells, the transcription of miR-424 and miR-503 increases after thyroid hormone binds to its receptor, further confirming its role in promoting tumor proliferation and invasion.54 miR-424 targets TGFBR3, thereby promoting EMT and migration of tongue squamous cell carcinoma (TSCC).55 miR-424-5p is involved in the invasion and metastasis of esophageal squamous cell carcinoma (ESCC) through the SMAD7 pathway; therefore, the upregulation of miR-424-5p may reduce the invasion and metastasis of the tumor.56 miR-424-5p affects the ERK1/2 signaling pathway by negatively regulating SOCS6 in pancreatic cancer, thereby increasing proliferation, migration, and invasion, and inhibiting apoptosis.57

There are relatively few studies on miR-424 in the urinary system. In prostate cancer, a study has found that low expression of miR-424-3p is closely related to increased invasiveness.24 Moreover, the expression level of miR-424 was shown to significantly correlate with aggressive tumor growth, advanced clinical stage, and poor prognosis of bladder cancer.58 In kidney cancer, miR-424 and miR-381 jointly target WEE1, up-regulate the activity of Cdc2 to synergistically inhibit the proliferation and survival of renal cancer cells, and participate in tumor-related processes.59 In basal-like breast cancer, a study has found that miR-424-5p regulates tumor cell proliferation, migration, and invasion by targeting doublecortin like kinase 1 (DCLK1).60 In the respiratory system, non-small cell lung cancer accounts for approximately 80% of all lung cancer cases. In the past few decades, the average survival time of patients diagnosed with non-small cell lung cancer (NSCLC) is less than 6 months.61 Another study found that miR-424 promotes the progression and metastasis of non-small cell lung cancer by regulating the tumor suppressor gene TNFAIP1.62 miR-424 can inhibit the proliferation and invasion of NSCLC by inhibiting the expression of E2F6.63 In the motor system, a study group demonstrated that miR-424 inhibits osteosarcoma cell migration and invasion by targeting fatty acid synthase.64

Drug Resistance and Radio-Sensitivity of Radiotherapy

Drug resistance is the main obstacle to the long-term effectiveness of cancer treatment. Drug resistance is mainly due to the generation of drug-resistant cells in the tumor tissue, which in turn leads to chemotherapeutic drugs being unable to exert a full anti-cancer effect. However, even if most of the tumor cells are killed, this small population of drug-resistant tumor cells will continue to proliferate, ultimately causing cancer relapse. In summary, following the emergence of drug resistance, the efficacy of chemotherapy will gradually decline, and eventually malignant tumors will no longer be treatable. In the reproductive system, studies have found that high expression of miR-424 and miR-503 is closely related to chemoresistance and tumor progression of ovarian cancer.65 miR-424-3p increases the sensitivity of the ovarian cancer cells SK-OV-3 and TOV-21G to cisplatin by reducing the expression of galectin-3 (anti-apoptotic protein); these results indicate that miR-424-3p may be an appropriate target to recover the sensitivity to chemotherapy drugs.66

Studies have found that the sensitivity of the commonly used chemotherapy drug, docetaxel, is affected by miR-424.67 Further research confirmed that miR-424 is involved in the regulation of PD-L1/PD-1 and CD80/CTLA-4 in chemotherapy-resistant ovarian cancer.68 In the endocrine system, miR-424-5p inactivates Hippo signaling, thereby promoting anoikis drug resistance and lung metastasis. Therefore, miR-424-5p has the potential to become a therapeutic target for lung metastases from thyroid cancer.69 A study in hormone receptor-positive metastatic breast cancer found that miR-424-5p can be used as a potential indicator of the sensitivity response to dovitinib.70 Furthermore, the deletion of miR-424 (322)/503 can promote breast cancer resistance by up-regulating its two targets: BCL-2 and insulin-like growth factor-1 receptor (IGF1R).71 In the digestive system, preliminary verification based on the GEO database and human gastric cancer tissues showed that miR-424 regulates gastric cancer cisplatin resistance by targeting SMURF1.72 In non-small cell lung cancer, studies have confirmed that the deletion of miR-424-3p is involved in chemotherapy resistance by targeting YAP1.73 In addition to chemotherapy resistance, the decline of tumor sensitivity to radiotherapy after long-term treatment has also attracted increasing attention. Studies have found that miR-424 can promote IR-induced DNA damage, apoptosis, and G2/M cell cycle arrest through APTX, thereby enhancing the radiation sensitivity of radiation-resistant cervical cancer cells.74

Cell Cycle

The cell cycle is the time required from the end of cell division to the end of the next cell division. The cell cycle is divided into four stages: G1 phase (gap1), which refers to the gap time before DNA replication is due to complete from mitosis; S phase (synthesis phase), which refers to the period of DNA replication; G2 phase (gap2), which refers to the completion of DNA replication but before the onset of mitosis; M phase, also known as D phase (mitosis or division), begins to end cell division. Dysregulation of the cell cycle is one of the main mechanisms of tumorigenesis.

A study identified that miR-424 in the digestive system regulates the cell cycle of esophageal squamous cell carcinoma (ESCC) to promote proliferation, and can be used as a new prognostic marker and an effective therapeutic target.75 In gastric cancer, miR-424-5p regulates the TGF-β signaling pathway and cyclin (c-Myc, CDK2, CDK4, CDK6) through SMAD3, where it has roles in regulating the cell cycle.76 Meanwhile, in the motion system, miR-424 suppressed the development of osteosarcoma by targeting the expression of cyclin cell A2.77 In epithelial ovarian cancer, miR-424-5p suppresses the expression of CCNE1, and blocks cells in the G1/G0 phase through the E2F1-pRb pathway.41 In conclusion, some studies have shown that miR-424 plays an important role in regulating the cell cycle, and can regulate the expression of miR-424 to inhibit the occurrence and development of tumors.

Stem Cell Properties

Cancer stem cells (CSCs) represent a subset of the cancer cell population that possess self-renewal ability and account for cancer initiation, progression, metastasis, and recurrence. It has been shown that in breast cancer cells, hyperglycemia can excessively activate tumor stem cells through the miR-424/cdc42/prdm14 axis, and enhance tumor invasion.78 Similarly, in another common endocrine-related tumor, prostate cancer, miR-424 targets E3 ubiquitin ligase COP1 and recognizes STAT3 as a key substrate of COP1, promoting prostate epithelial cell tumorigenicity and cancer stem cell-like properties.79

Relationship with Viruses

Various viruses have been shown to be closely related to the occurrence of tumors. EBV was the first human virus to be shown to be directly related to canceration, which has been shown to be closely related to various malignant tumors.80 The causal relationship between human papillomavirus (HPV) and cervical cancer is well established in biology and epidemiology. HPV-16 and −18 infections account for approximately 70% of cervical cancer cases.81 A previous study reported that miR-424 plays a key role in the regulation of HPV replication. Furthermore, HPV E6 and E7 proteins inhibit miR-424 levels, control CHK1, and have been shown to play a central role in viral replication.37 Furthermore, the interaction between HPV16 and E7CUL2 recruits CUL2 and activates the regulatory loops between CUL2, E2F1, and miR-424, which results in persistent CUL2 overexpression, and subsequent promotion of HPV16-induced cervical cancer development.82

In conclusion, existing evidence indicates that miR-424 plays an important role in various stages of tumorigenesis. Moreover, analysis of miR-424 expression can help to diagnose diseases, and has the potential to become an important molecule in tumor diagnosis and prognosis. In addition, in the future, the expression of miR-424 may be adjusted to regulate the occurrence and development of tumors and limit tumor progression. Taken together, these studies have suggested that miR-424 performs different functions in various cancers (Table 1).

Table 1.

The Function of the Target Gene of miR-424 in Difference Cancers

Cancer Type Target Genes Related Function References
Bladder cancer EGFR EMT [24]
HCC TRIM29 proliferation and invasion [28]
Glioma KIF23 migration, invasion and EMT [34]
Cervical cancer CHEK1 HPV replication [35]
Cervical cancer KDM5B growth proliferation apoptosis [36]
Cervical cancer Chk1 proliferation,apoptosis,suppressed cell-cycle progression [37]
Endometrial cancer E2F7 proliferation, apoptosis and cell arrest [38]
Endometrial cancer NSD2 invasion and sphere formation [39]
Ovarian cancer CCNE1 cell cycle [41]
Ovarian cancer DCLK1 proliferation, migration, invasion and EMT [42]
Colorectal cancer CCNE1 malignant behavior [45]
Colorectal cancer AKT3 PSAT1 tumor-suppressive apoptosis [46]
Colorectal cancer SCN4B proliferation and metastasis [47]
Prostate and colon cancer RICTOR tumorigenicity and invasive [48]
Intrahepatic cholangiocarcinoma ARK5 metastasis and invasion [49]
HCC YAP1 proliferation and apoptosis [50]
HCC MYB proliferation,migration and invasion [52]
HCC AKT3 proliferation and apoptosis [53]
Tongue squamous cell carcinoma TGFBR3 EMT and migration [55]
Esophageal squamous cell carcinoma SAMD7 EMT [56]
Pancreatic cancer SOCS6 proliferation, migration,invasion and apoptosis [57]
Renal cancer WEE1 mitotic entry and apoptosis [59]
Breast cancer DCLK1 proliferation, migration and invasion [60]
NSCLC TNFAIP1 progression and metastasis [62]
NSCLC E2F6 proliferation and migration Abilities [63]
Osteosarcoma FASN migration and invasion [64]
Ovarian cancer LGALS3 chemoresistance and apoptosis [66]
Ovarian cancer PD-L1 chemoresistance [68]
Ovarian cancer PD-L1 PD-1 CD80 CTLA-4 chemoresistance [68]
Thyroid cancer WWC1 SAV1 LATS2 chemoresistance and metastasis [69]
Breast cancer IGF1R BCL-2 epithelial involution, tumorigenesis, and the phenomenon of chemoresistance [71]
Gastric cancer SMURF1 chemoresistance [72]
NSCLC YAP1 chemoresistance [73]
Cervical cancer APTX radiosensitize [74]
Esophageal squamous cell carcinoma PRKCD WEE1 cell cycle [75]
Osteosarcoma PCNA cell cycle and proliferation [77]
Breast cancer CDC42 distant metastasis and mortality [78]
Prostate cancer STAT3 EMT and stem cell–like features [79]
Cervical carcinogenesis CLU2 proliferation [82]
Ovarian cancer ESR1 proliferation and invasion [83]
Gastric cancer E2F1 tumorigenesis and cell cycle [88]
NSCLC CARM1 proliferation,invasion,apoptosis and proliferation [91]
NSCLC PLSCR4 proliferation and apoptosis [92]
Glioma CHEK1 chemosensitivity [93]
Glioma VEGFA angiogenesis [94]
Invasive neuroendocrine tumor FGF2 proliferation, migration, invasion and apoptosis [96]
Gastric cancer LATS1 proliferation and invasion [98]
Open in a new tab

Molecules That Regulate the Expression of miR-424 in Tumors

LncRNA

Accumulating evidence has shown that a variety of lncRNAs and cirRNAs are involved in the occurrence and development of tumors by regulating mir-424. For example, in the reproductive system, estrogen receptor 1 (ESR1) plays an important role in the pathological process of ovarian cancer. ESR1-induced upregulation of LINC00511 may be caused by sponged miR-424-5p and miR-370- 5p, which in turn promotes the proliferation and invasion of ovarian cancer CAOV3 cells.83 Moreover, it has been shown that Lnc-SNHG12 negatively regulates miR-424-5p to promote cancer.84 Another study found that Lnc-CCAT2 negatively targets miR-424 as a competitive endogenous RNA (ceRNA) or sponge for ovarian cancer, and represents a new diagnostic marker and therapeutic target.85 Tumor promoting effects of Lnc-PVT1 were found in cervical cancer, as competitive endogenous RNA (ceRNA) or molecular sponge negatively regulates miR-424.86 Furthermore, LncRNA BLACAT1 expression is increased in cervical cancer (CSCC), while BLACAT1 overexpression may promote tumor progression by down-regulating miR-424.87 Another study found that the tumor-promoting Small nucleolar RNA host gene 12 (SNHG12) acts as a molecular sponge of miR-424-5p and has a negative regulatory effect.84 With regards to the digestive system, Lnc-RNA NNT-AS1 can affect the tumorigenesis and cell cycle of gastric cancer cells by binding to miR-424/E2F1.88 Moreover, in hepatocellular carcinoma, LncRNA-LINC00511 plays an important role in the malignant progression of HCC by regulating miR-424.89 Another study has found that Lnc-RNA DLX6-AS1 increases the expression of WEE1 by targeting miR-424-5p, which in turn promotes hepatocellular carcinoma.90 In the respiratory system, non-small cell lung cancer accounts for approximately 80% of lung cancer subclasses, and is the disease with the highest cancer-related mortality in both men and women. A research team found that the miR-424-5p/lncRNA PVT1/CARM1 axis can influence non-small cell lung cancer. Furthermore, radiotherapy sensitivity of small cell lung carcinoma, overexpression of miR-424-5p, or inhibition of lncRNA PVT1 can increase the radiotherapy sensitivity of NSCLC.91 Lnc-RNA LINC00641 was found to inhibit the progression of non-small cell lung cancer by sponging miR-424-5p and up-regulating PLSCR4. Further rescue experiments showed that miR-424-5p and PLSCR4 can reverse the cell process mediated by LINC00641. In conclusion, LINC00641 exerts a tumor suppressive effect in NSCLC through miR-424-5p.92

In the central nervous system, a previous study demonstrated that lncRNA-CCAT2 enhances the chemoresistance of glioma cells through the lncRNA-CCAT2/miR-424/Chk1 axis, and promotes the migration of glioma cells. As such, the curative effect of chemotherapy for glioma can be improved by inhibiting this axis.93 Recent studies have found that lncRNA-CCAT2 also can down-regulate miR-424 to promote VEGFA expression, induce PI3K/AKT signaling, and promote cell proliferation and endothelial angiogenesis.94 It was also found that down-regulation of lncRNA-PVT1 inhibits the progression of glioma by up-regulating the expression of miR-424.95 In addition, in invasive pituitary neuroendocrine tumors, LncRNA-XIST competitively combines with miR-424-5p to increase the expression of bFGF to promote cell proliferation, migration, invasion, and inhibit cell cycle arrest and apoptosis.96 In the circulatory system, a research group used tumor xenograft experiments to show that LncRNA-MALAT1 inhibits miR-424 and activates the MEKK3-mediated IKK/NF-kappaB pathway to promote the development of hemangioma. This suggests that LncRNA-MALAT1, miR-424, and MEKK3 can be used as potential targets for the improvement of IH treatment efficiency.97

CircRNA

In addition to LncRNA, part of CircRNA is also involved in the regulation of microRNA. Circ-LARP4 inhibits the proliferation and invasion of gastric cancer cells by sponging miR-424-5p and regulating the expression of LATS1. The increased expression of miR-424 or the decreased expression of LATS1, is closely related to the pathological stage and poor prognosis of GC patients.98 Studies have also found that the high expression of Circ-LARP4 is related to a shorted perioperative period and prolonged survival of osteosarcoma, as well as increased chemical sensitivity to cisplatin and doxorubicin through cavernous miR-424.99 In short, an increasing number of circ-RNAs have been shown to be involved in the regulation of miR-424, and their function needs to be explored further.

Taken together, these studies have suggested that miR-424 regulated by different non-coding RNA in various cancers (Table 2).

Table 2.

The Function of the Upstream Genes of miR-424 in Difference Cancers

Cancer Upstream Genes Function Reference
Ovarian cancer Long Non-Coding RNA LINC00511 proliferation and invasion [83]
Cervical cancer Small nucleolar RNA host gene 12 (SNHG12) proliferation, apoptosis, migration and invasion [84]
Ovarian cancer Long Noncoding RNA CCAT2 proliferation and apoptosis [85]
Cervical cancer lncRNA PVT1 proliferation, colony formation, migration and invasion [86]
CSCC LncRNA BLACAT1 migration and invasion [87]
Gastric cancer Long non‐coding RNA NNT‐AS1 tumorigenesis and cell cycle [88]
HCC Long Non-Coding RNA LINC00511 nodal metastasis, vascular invasion and clinical stage [89]
HCC Long noncoding RNA DLX6‐AS1 proliferation, migration and invasion [90]
NSCLC Long Non-coding RNA PVT1 proliferation,invasion,apoptosis and proliferation [91]
NSCL Long non-coding RNA LINC00641 proliferation and apoptosis [92]
Glioma lncRNA CCAT2 chemoresistance [93]
Glioma lncRNA CCAT2 angiogenesis [94]
Glioma lncRNA PVT1 migration and invasion [95]
Neuroendocrine tumor LncRNA XIST proliferation, migration, invasion and apoptosis [96]
Infantile hemangioma LncRNA-MALAT1 proliferation, apoptosis, migration and invasion [97]
Gastric cancer Circular RNA LARP4 proliferation and invasion [98]
Osteosarcoma Circular RNA LARP4 chemoresistance [99]
Open in a new tab

Bioinformatics Analysis of miR-424

We performed KEGG pathway analysis of miR-424 using Webgestalt (http://bioinfo.vanderbilt.edu/webgestalt/) to predict the possible downstream pathway of miR-424 target genes, screening is performed with P < 0.05 as the critical value. After KEGG analysis, the 20 most relevant routes were selected, 15 of which were found to have significant P-values. The 20 KEGG pathways with the highest concentration are shown in Figure 1A. miR-424 target genes were mainly enriched in the Hippo signaling pathway, pancreatic cancer, EGFR tyrosine kinase inhibitor resistance, AGE-RAGE signaling pathways in diabetic complications, Hepatitis B, proteoglycans in cancer, cell cycle, and several cancer-related pathways. These data indicated that miR-424-5p might play important roles in the malignant behavior of cancer. Among them, Hippo signaling pathway affected the genesis and development of tumors by regulating cell proliferation, apoptosis and stem cell self-renewal ability.100,101 In addition, miR-424 regulates tumor proliferation and invasion processes by regulating EGFR. A research has revealed a wide range of role of EGFR via adding EGF to cultured HeLa cells to activate EGFR resulting in phosphorylation of 6600 sites in 2244 proteins.102 After ligand binding, the intracellular tyrosine sites of EGFR are phosphorylated, which consequently match to different signal transduction proteins to initiate different signal pathways.103 The intricate signal transduction network play roles in tumor cell proliferation, metastasis and anti-apoptosis.104 Therefore, overexpression or mutation of EGFR is closely related to the pathogenesis of cancer and the poor prognosis of patients.

Figure 1.

Figure 1

Open in a new tab

(A) KEGG analysis showing the number of transcripts mapped to the function involved in the target genes of miR-424. The 20 KEGG pathways most strongly enriched by functional-related gene groups. (B) The competing endogenous RNA network of cirRNA/lncRNA-microRNA-mRNA. The pink dots represent target genes of miR-424. The green dots represents lncRNA, while the orange dots diamonds represent cirRNA. The blue dots represents the miR-424-5p or miR-424-3p.

In sum, miR-424 participates in downstream target genes through regulation, and then plays an important role in the malignant behavior of cancer. If we can further clarify the relationship between miR-424 and downstream pathways and the mechanism of action between pathways, we will clarify the potential molecular mechanism of miR-424 involved in regulating the occurrence and development of malignant tumors. It will be beneficial to tumor diagnosis and treatment. Next, we carried out the construction of ce-network (Figure 1B), combined with the above review and network diagram, we clearly found that miRNAs in organisms not only play a regulatory role on downstream target genes at the post-transcriptional level, but also their expression and function are affected by multiple signal transduction pathways and transcription factors. The regulatory relationship between them is related to each other through a complex linear relationship of point-to-multipoint divergence or multipoint-to-point convergence. The body constitutes a network-type deployment control to play its corresponding physiological or pathological role.

Discussion

In recent years, the role of miRNA in the occurrence, development, and diagnosis of diseases has attracted considerable attention, and evidence for the association between miRNA and the occurrence and development of tumors is only increasing. In line with this, miR-424 has been a hotspot in the field of cancer research, and evidence shows that it is closely related to the biological processes of tumor cell proliferation, migration, invasion, and apoptosis, as well as tumor occurrence, development, diagnosis and treatment, chemosensitivity and recurrence monitoring, prognosis assessment, and viral infections. We employed the use of bioinformatics to show the KEGG pathway of miR-424 based on the reported mRNA reported in the literature, as well as the competing endogenous RNA network of cirRNA/lncRNA-microRNA-mRNA. miR-424 can act as either a cancer-promoting factor or a tumor suppressor. miR-424 regulates multiple mRNAs and affects multiple signal transduction pathways, while the target genes regulated by miRNA in different microenvironments are also different. The multiple target gene pathways are related to each other, and the relationship is extremely complex. Therefore, further studies are needed to clarify the precise function of miR-424 in tumors. In order to reduce the side effects of miRNA binding to other targets during cancer treatment, it is necessary to develop highly specific miRNA. In addition, to ensure that the drug can function safely and effectively after reaching the body, the design of the drug carrier needs to be continuously improved and perfected. In view of the potential value of miR-424 in the clinical application of cancer, future applied research needs to further explore the application value of miR-424 in the prevention, diagnosis, prognosis, and targeted therapy of malignant tumors. This will ultimately lead to more promising treatment opportunities for accurate diagnosis and safe and effective options for the long-term treatment of patients with tumors.

Acknowledgments

The study was sponsored by the Science and Technology Innovation Commission Foundation of Shenzhen (Grant No. JCYJ20190808141013454 and JCYJ20180305124827261)

Disclosure

The authors report no conflicts of interest in this work.

References

  • 1.Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell. 1993;75:843–854. [DOI] [PubMed] [Google Scholar]
  • 2.Pillai RS, Bhattacharyya SN, Filipowicz WJT. Repression of protein synthesis by miRNAs: how many mechanisms? Trend Cell Biol. 2007;17:118–126. [DOI] [PubMed] [Google Scholar]
  • 3.Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell. 2009;136:215–233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Garzon R, Calin GA, Croce CMJ. MicroRNAs in cancer. Annu Rev Med. 2009;60:167–179. [DOI] [PubMed] [Google Scholar]
  • 5.Carthew RW, Sontheimer EJ. Origins and mechanisms of miRNAs and siRNAs. Cell. 2009;136:642–655. doi: 10.1016/j.cell.2009.01.035 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Lee Y, Kim M, Han J, et al. MicroRNA genes are transcribed by RNA polymerase II. EMBO J. 2004;23:4051–4060. doi: 10.1038/sj.emboj.7600385 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Lee Y, Ahn C, Han J, et al. The nuclear RNase III Drosha initiates microRNA processing. Nature. 2003;425:415–419. doi: 10.1038/nature01957 [DOI] [PubMed] [Google Scholar]
  • 8.Carmell MA, Hannon GJ. RNase III enzymes and the initiation of gene silencing. Nat Struct Mol Biol. 2004;11:214–218. doi: 10.1038/nsmb729 [DOI] [PubMed] [Google Scholar]
  • 9.Gregory RI, Yan K-P, Amuthan G, et al. The Microprocessor complex mediates the genesis of microRNAs. Nature. 2004;432:235–240. doi: 10.1038/nature03120 [DOI] [PubMed] [Google Scholar]
  • 10.Bernstein E, Caudy AA, Hammond SM, Hannon GJ. Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature. 2001;409:363–366. doi: 10.1038/35053110 [DOI] [PubMed] [Google Scholar]
  • 11.Khvorova A, Reynolds A, Jayasena SD. Functional siRNAs and miRNAs exhibit strand bias. Cell. 2003;115:209–216. doi: 10.1016/S0092-8674(03)00801-8 [DOI] [PubMed] [Google Scholar]
  • 12.John B, Enright AJ, Aravin A, Tuschl T, Sander C, Marks DS. Human microRNA targets. PLoS Biol. 2004;2:e363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Krek A, Grun D, Poy MN, et al. Combinatorial microRNA target predictions. Nat Genet. 2005;37:495–500. doi: 10.1038/ng1536 [DOI] [PubMed] [Google Scholar]
  • 14.Mogilyansky E, Rigoutsos I. The miR-17/92 cluster: a comprehensive update on its genomics, genetics, functions and increasingly important and numerous roles in health and disease. Cell Death Differ. 2013;20:1603–1614. doi: 10.1038/cdd.2013.125 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lewis BP, Burge CB, Bartel DP. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell. 2005;120:15–20. [DOI] [PubMed] [Google Scholar]
  • 16.Baek D, Villén J, Shin C, Camargo FD, Gygi SP, Bartel DPJN. The impact of microRNAs on protein output. Nature. 2008;455:64–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Selbach M, Schwanhäusser B, Thierfelder N, Fang Z, Khanin R, Rajewsky N. Widespread changes in protein synthesis induced by microRNAs. Nature. 2008;455:58–63. [DOI] [PubMed] [Google Scholar]
  • 18.Zhao K, Chen Y, Yang R, et al. miR-424/322 is downregulated in the semen of patients with severe DNA damage and may regulate sperm DNA damage. Reprod Fertil Dev. 2016;28:1598–1607. doi: 10.1071/RD15052 [DOI] [PubMed] [Google Scholar]
  • 19.Tsuru Y, Jinnin M, Ichihara A, et al. miR‐424 levels in hair shaft are increased in psoriatic patients. J Dermatol. 2014;41:382–385. [DOI] [PubMed] [Google Scholar]
  • 20.de Andrade HM, de Albuquerque M, Avansini SH, et al. MicroRNAs-424 and 206 are potential prognostic markers in spinal onset amyotrophic lateral sclerosis. J Neurol Sci. 2016;368:19–24. doi: 10.1016/j.jns.2016.06.046 [DOI] [PubMed] [Google Scholar]
  • 21.Min K-H, Yang W-M, Lee WJB. Saturated fatty acids-induced miR-424–5p aggravates insulin resistance via targeting insulin receptor in hepatocytes. Biochem Biophys Res Commun. 2018;503:1587–1593. doi: 10.1016/j.bbrc.2018.07.084 [DOI] [PubMed] [Google Scholar]
  • 22.Cheng D, Zhu C, Liang Y, Xing Y, Shi C. MiR-424 overexpression protects alveolar epithelial cells from LPS-induced apoptosis and inflammation by targeting FGF2 via the NF-κB pathway. Life Sci. 2020;242:117213. doi: 10.1016/j.lfs.2019.117213 [DOI] [PubMed] [Google Scholar]
  • 23.Hirschfeld M, Rucker G, Weiss D, et al. Urinary exosomal microRNAs as potential non-invasive biomarkers in breast cancer detection. Mol Diagn Ther. 2020;24:215–232. doi: 10.1007/s40291-020-00453-y [DOI] [PubMed] [Google Scholar]
  • 24.Richardsen E, Andersen S, Al-Saad S, et al. Low expression of miR-424-3p is highly correlated with clinical failure in prostate cancer. Sci Rep. 2019;9:10662. doi: 10.1038/s41598-019-47234-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Suer I, Guzel E, Karatas OF, Creighton CJ, Ittmann M, Ozen M. MicroRNAs as prognostic markers in prostate cancer. Prostate. 2019;79:265–271. doi: 10.1002/pros.23731 [DOI] [PubMed] [Google Scholar]
  • 26.Lyu J, Zhao L, Wang F, et al. Discovery and validation of serum microRNAs as early diagnostic biomarkers for prostate cancer in Chinese population. Biomed Res Int. 2019;2019:9306803. doi: 10.1155/2019/9306803 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Wang ZX, Deng TX, Ma Z. Identification of a 4-miRNA signature as a potential prognostic biomarker for pancreatic adenocarcinoma. J Cell Biochem. 2019;120:16416–16426. doi: 10.1002/jcb.28601 [DOI] [PubMed] [Google Scholar]
  • 28.Du H, Xu Q, Xiao S, et al. MicroRNA-424-5p acts as a potential biomarker and inhibits proliferation and invasion in hepatocellular carcinoma by targeting TRIM29. Life Sci. 2019;224:1–11. doi: 10.1016/j.lfs.2019.03.028 [DOI] [PubMed] [Google Scholar]
  • 29.Lu M, Kong X, Wang H, Huang G, Ye C, He Z. A novel microRNAs expression signature for hepatocellular carcinoma diagnosis and prognosis. Oncotarget. 2017;8:8775–8784. doi: 10.18632/oncotarget.14452 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Yao H, Liu X, Chen S, Xia W, Chen X. Decreased expression of serum miR-424 correlates with poor prognosis of patients with hepatocellular carcinoma. Int J Clin Exp Pathol. 2015;8:14830–14835. [PMC free article] [PubMed] [Google Scholar]
  • 31.Wu L, Yang F, Lin B, et al. MicroRNA-424 expression predicts tumor recurrence in patients with hepatocellular carcinoma following liver transplantation. Oncol Lett. 2018;15:9126–9132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Wang Y, Lv Z, Fu J, Wang Z, Fan Z, Lei T. Endogenous microRNA-424 predicts clinical outcome and its inhibition acts as cancer suppressor in human non-small cell lung cancer. Biomed Pharmacother. 2017;89:208–214. doi: 10.1016/j.biopha.2017.01.163 [DOI] [PubMed] [Google Scholar]
  • 33.Jin C, Li M, Ouyang Y, Tan Z, Jiang Y. MiR-424 functions as a tumor suppressor in glioma cells and is down-regulated by DNA methylation. J Neurooncol. 2017;133:247–255. doi: 10.1007/s11060-017-2438-4 [DOI] [PubMed] [Google Scholar]
  • 34.Zhao C, Wang XB, Zhang YH, Zhou YM, Yin Q, Yao WC. MicroRNA-424 inhibits cell migration, invasion and epithelial-mesenchymal transition in human glioma by targeting KIF23 and functions as a novel prognostic predictor. Eur Rev Med Pharmacol Sci. 2018;22:6369–6378. [DOI] [PubMed] [Google Scholar]
  • 35.Hong S, Cheng S, Songock W, Bodily J, Laimins LA. Suppression of microRNA 424 levels by human papillomaviruses is necessary for differentiation-dependent genome amplification. J Virol. 2017;91. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Zhou Y, An Q, Guo RX, et al. miR424-5p functions as an anti-oncogene in cervical cancer cell growth by targeting KDM5B via the Notch signaling pathway. Life Sci. 2017;171:9–15. doi: 10.1016/j.lfs.2017.01.006 [DOI] [PubMed] [Google Scholar]
  • 37.Xu J, Li Y, Wang F, et al. Suppressed miR-424 expression via upregulation of target gene Chk1 contributes to the progression of cervical cancer. Oncogene. 2013;32:976–987. doi: 10.1038/onc.2012.121 [DOI] [PubMed] [Google Scholar]
  • 38.Li Q, Qiu XM, Li QH, et al. MicroRNA-424 may function as a tumor suppressor in endometrial carcinoma cells by targeting E2F7. Oncol Rep. 2015;33:2354–2360. doi: 10.3892/or.2015.3812 [DOI] [PubMed] [Google Scholar]
  • 39.Dong P, Xiong Y, Yue J, Hanley SJB, Watari H. miR-34a, miR-424 and miR-513 inhibit MMSET expression to repress endometrial cancer cell invasion and sphere formation. Oncotarget. 2018;9:23253–23263. doi: 10.18632/oncotarget.25298 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Lu Z, Nian Z, Jingjing Z, Tao L, Quan L. MicroRNA-424/E2F6 feedback loop modulates cell invasion, migration and EMT in endometrial carcinoma. Oncotarget. 2017;8:114281–114291. doi: 10.18632/oncotarget.23218 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Liu J, Gu Z, Tang Y, Hao J, Zhang C, Yang X. Tumour-suppressive microRNA-424-5p directly targets CCNE1 as potential prognostic markers in epithelial ovarian cancer. Cell Cycle. 2018;17:309–318. doi: 10.1080/15384101.2017.1407894 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Wu X, Ruan Y, Jiang H, Xu C. MicroRNA-424 inhibits cell migration, invasion, and epithelial mesenchymal transition by downregulating doublecortin-like kinase 1 in ovarian clear cell carcinoma. Int J Biochem Cell Biol. 2017;85:66–74. doi: 10.1016/j.biocel.2017.01.020 [DOI] [PubMed] [Google Scholar]
  • 43.Li Y, Liu J, Hu W, et al. miR-424-5p promotes proliferation, migration and invasion of laryngeal squamous cell carcinoma. Onco Targets Ther. 2019;12:10441–10453. doi: 10.2147/OTT.S224325 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Peng H-Y, Jiang -S-S, Hsiao J-R, et al. IL-8 induces miR-424-5p expression and modulates SOCS2/STAT5 signaling pathway in oral squamous cell carcinoma. Mol Oncol. 2016;10:895–909. doi: 10.1016/j.molonc.2016.03.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Jiang B, Wu D, Huang L, Fang H. miR-424-5p inhibited malignant behavior of colorectal cancer cells by targeting CCNE1. Panminerva Med. 2019. [DOI] [PubMed] [Google Scholar]
  • 46.Fang Y, Liang X, Xu J, Cai X. miR-424 targets AKT3 and PSAT1 and has a tumor-suppressive role in human colorectal cancer. Cancer Manag Res. 2018;10:6537–6547. doi: 10.2147/CMAR.S185789 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Dai W, Zhou J, Wang H, Zhang M, Yang X, Song W. miR-424-5p promotes the proliferation and metastasis of colorectal cancer by directly targeting SCN4B. Pathol Res Pract. 2020;216:152731. doi: 10.1016/j.prp.2019.152731 [DOI] [PubMed] [Google Scholar]
  • 48.Oneyama C, Kito Y, Asai R, et al. MiR-424/503-mediated Rictor upregulation promotes tumor progression. PLoS One. 2013;8:e80300. doi: 10.1371/journal.pone.0080300 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Wu J, Yang B, Zhang Y, et al. miR-424-5p represses the metastasis and invasion of intrahepatic cholangiocarcinoma by targeting ARK5. Int J Biol Sci. 2019;15:1591–1599. doi: 10.7150/ijbs.34113 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Piao L, Wang F, Wang Y, et al. miR-424-5p regulates hepatoma cell proliferation and apoptosis. Cancer Biother Radiopharm. 2019;34:196–202. doi: 10.1089/cbr.2018.2625 [DOI] [PubMed] [Google Scholar]
  • 51.Zhang Y, Li T, Guo P, et al. MiR-424-5p reversed epithelial-mesenchymal transition of anchorage-independent HCC cells by directly targeting ICAT and suppressed HCC progression. Sci Rep. 2014;4:6248. doi: 10.1038/srep06248 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Yu L, Ding GF, He C, Sun L, Jiang Y, Zhu L. MicroRNA-424 is down-regulated in hepatocellular carcinoma and suppresses cell migration and invasion through c-Myb. PLoS One. 2014;9:e91661. doi: 10.1371/journal.pone.0091661 [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
  • 53.Yang H, Zheng W, Shuai X, et al. MicroRNA-424 inhibits Akt3/E2F3 axis and tumor growth in hepatocellular carcinoma. Oncotarget. 2015;6:27736–27750. doi: 10.18632/oncotarget.4811 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Ruiz-Llorente L, Ardila-Gonzalez S, Fanjul LF, Martinez-Iglesias O, Aranda A. microRNAs 424 and 503 are mediators of the anti-proliferative and anti-invasive action of the thyroid hormone receptor beta. Oncotarget. 2014;5:2918–2933. doi: 10.18632/oncotarget.1577 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Li D, Liu K, Li Z, Wang J, Wang X. miR-19a and miR-424 target TGFBR3 to promote epithelial-to-mesenchymal transition and migration of tongue squamous cell carcinoma cells. Cell Adh Migr. 2018;12:236–246. doi: 10.1080/19336918.2017.1365992 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Wang F, Wang J, Yang X, Chen D, Wang L. MiR-424-5p participates in esophageal squamous cell carcinoma invasion and metastasis via SMAD7 pathway mediated EMT. Diagn Pathol. 2016;11:88. doi: 10.1186/s13000-016-0536-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Wu K, Hu G, He X, et al. MicroRNA-424-5p suppresses the expression of SOCS6 in pancreatic cancer. Pathol Oncol Res. 2013;19:739–748. doi: 10.1007/s12253-013-9637-x [DOI] [PubMed] [Google Scholar]
  • 58.Wu CT, Lin WY, Chang YH, Lin PY, Chen WC, Chen MF. DNMT1-dependent suppression of microRNA424 regulates tumor progression in human bladder cancer. Oncotarget. 2015;6:24119–24131. doi: 10.18632/oncotarget.4431 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Chen B, Duan L, Yin G, Tan J, Jiang X. Simultaneously expressed miR-424 and miR-381 synergistically suppress the proliferation and survival of renal cancer cells—Cdc2 activity is up-regulated by targeting WEE1. Clinics (Sao Paulo). 2013;68:825–833. doi: 10.6061/clinics/2013(06)17 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Wang J, Wang S, Zhou J, Qian Q. miR-424-5p regulates cell proliferation, migration and invasion by targeting doublecortin-like kinase 1 in basal-like breast cancer. Biomed Pharmacother. 2018;102:147–152. [DOI] [PubMed] [Google Scholar]
  • 61.Devesa SS, Bray F, Vizcaino AP, Parkin DM. International lung cancer trends by histologic type: male: female differences diminishing and adenocarcinoma rates rising. Int J Cancer. 2005;117:294–299. doi: 10.1002/ijc.21183 [DOI] [PubMed] [Google Scholar]
  • 62.Zhang M, Gao C, Yang Y, et al. MiR-424 promotes non-small cell lung cancer progression and metastasis through regulating the tumor suppressor gene TNFAIP1. Cell Physiol Biochem. 2017;42:211–221. doi: 10.1159/000477314 [DOI] [PubMed] [Google Scholar]
  • 63.Li H, Lan H, Zhang M, et al. [Effects of miR-424 on proliferation and migration abilities in non-small cell lung cancer A549 cells and its molecular mechanism]. Zhongguo Fei Ai Za Zhi. 2016;19:571–576. Chinese. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Long XH, Mao JH, Peng AF, Zhou Y, Huang SH, Liu ZL. Tumor suppressive microRNA-424 inhibits osteosarcoma cell migration and invasion via targeting fatty acid synthase. Exp Ther Med. 2013;5:1048–1052. doi: 10.3892/etm.2013.959 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Park YT, Jeong JY, Lee MJ, et al. MicroRNAs overexpressed in ovarian ALDH1-positive cells are associated with chemoresistance. J Ovarian Res. 2013;6:18. doi: 10.1186/1757-2215-6-18 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Bieg D, Sypniewski D, Nowak E, Bednarek I. MiR-424-3p suppresses galectin-3 expression and sensitizes ovarian cancer cells to cisplatin. Arch Gynecol Obstet. 2019;299:1077–1087. doi: 10.1007/s00404-018-4999-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Geretto M, Pulliero A, Rosano C, Zhabayeva D, Bersimbaev R, Izzotti A. Resistance to cancer chemotherapeutic drugs is determined by pivotal microRNA regulators. Am J Cancer Res. 2017;7:1350–1371. [PMC free article] [PubMed] [Google Scholar]
  • 68.Xu S, Tao Z, Hai B, et al. miR-424(322) reverses chemoresistance via T-cell immune response activation by blocking the PD-L1 immune checkpoint. Nat Commun. 2016;7:11406. doi: 10.1038/ncomms11406 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Liu X, Fu Y, Zhang G, et al. miR-424-5p promotes anoikis resistance and lung metastasis by inactivating hippo signaling in thyroid cancer. Mol Ther Oncolytics. 2019;15:248–260. doi: 10.1016/j.omto.2019.10.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Shivapurkar N, Vietsch EE, Carney E, Isaacs C, Wellstein A. Circulating microRNAs in patients with hormone receptor-positive, metastatic breast cancer treated with dovitinib. Clin Transl Med. 2017;6:37. doi: 10.1186/s40169-017-0169-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Rodriguez-Barrueco R, Nekritz EA, Bertucci F, et al. miR-424(322)/503 is a breast cancer tumor suppressor whose loss promotes resistance to chemotherapy. Genes Dev. 2017;31:553–566. doi: 10.1101/gad.292318.116 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Lu L, Wu M, Lu Y, et al. MicroRNA-424 regulates cisplatin resistance of gastric cancer by targeting SMURF1 based on GEO database and primary validation in human gastric cancer tissues. Onco Targets Ther. 2019;12:7623–7636. doi: 10.2147/OTT.S208275 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Zhang M, Zeng J, Zhao Z, Liu Z. Loss of MiR-424-3p, not miR-424-5p, confers chemoresistance through targeting YAP1 in non-small cell lung cancer. Mol Carcinog. 2017;56:821–832. doi: 10.1002/mc.22536 [DOI] [PubMed] [Google Scholar]
  • 74.Wang X, Li Q, Jin H, et al. miR-424 acts as a tumor radiosensitizer by targeting aprataxin in cervical cancer. Oncotarget. 2016;7:77508–77515. doi: 10.18632/oncotarget.12716 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Wen J, Hu Y, Liu Q, et al. miR-424 coordinates multilayered regulation of cell cycle progression to promote esophageal squamous cell carcinoma cell proliferation. EBioMedicine. 2018;37:110–124. doi: 10.1016/j.ebiom.2018.10.043 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Wei S, Li Q, Li Z, Wang L, Zhang L, Xu Z. miR-424-5p promotes proliferation of gastric cancer by targeting Smad3 through TGF-β; signaling pathway . Oncotarget. 2016;7:75185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Shekhar R, Priyanka P, Kumar P, et al. The microRNAs miR-449a and miR-424 suppress osteosarcoma by targeting cyclin A2 expression. J Biol Chem. 2019;294:4381–4400. doi: 10.1074/jbc.RA118.005778 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Nandy SB, Orozco A, Lopez-Valdez R, et al. Glucose insult elicits hyperactivation of cancer stem cells through miR-424-cdc42-prdm14 signalling axis. Br J Cancer. 2017;117:1665–1675. doi: 10.1038/bjc.2017.335 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Dallavalle C, Albino D, Civenni G, et al. MicroRNA-424 impairs ubiquitination to activate STAT3 and promote prostate tumor progression. J Clin Invest. 2016;126:4585–4602. doi: 10.1172/JCI86505 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Thompson MP, Kurzrock R. Epstein-Barr virus and cancer. Clin Cancer Res. 2004;10:803–821. doi: 10.1158/1078-0432.CCR-0670-3 [DOI] [PubMed] [Google Scholar]
  • 81.Munoz N, Castellsagué X, de González AB, Gissmann L. HPV in the etiology of human cancer. Vaccine. 2006;24:S1–S10. doi: 10.1016/j.vaccine.2006.05.115 [DOI] [PubMed] [Google Scholar]
  • 82.Xu J, Fang Y, Wang X, et al. CUL2 overexpression driven by CUL2/E2F1/miR-424 regulatory loop promotes HPV16 E7 induced cervical carcinogenesis. Oncotarget. 2016;7:31520–31533. doi: 10.18632/oncotarget.9127 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Wang K, Zhu G, Bao S, Chen S. Long non-coding RNA LINC00511 mediates the effects of ESR1 on proliferation and invasion of ovarian cancer through miR-424-5p and miR-370-5p. Cancer Manag Res. 2019;11:10807–10819. doi: 10.2147/CMAR.S232140 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Dong J, Wang Q, Li L, Xiao-Jin Z. Upregulation of long non-coding RNA small nucleolar RNA host gene 12 contributes to cell growth and invasion in cervical cancer by acting as a sponge for MiR-424-5p. Cell Physiol Biochem. 2018;45:2086–2094. doi: 10.1159/000488045 [DOI] [PubMed] [Google Scholar]
  • 85.Hua F, Li CH, Chen XG, Liu XP. Long noncoding RNA CCAT2 knockdown suppresses tumorous progression by sponging miR-424 in epithelial ovarian cancer. Oncol Res. 2018;26:241–247. doi: 10.3727/096504017X14953948675412 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Gao YL, Zhao ZS, Zhang MY, Han LJ, Dong YJ, Xu B. Long noncoding RNA PVT1 facilitates cervical cancer progression via negative regulating of miR-424. Oncol Res. 2017;25:1391–1398. doi: 10.3727/096504017X14881559833562 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Cheng H, Tian J, Wang C, Ren L, Wang N. LncRNA BLACAT1 is upregulated in cervical squamous cell carcinoma (CSCC) and predicts poor survival. Reprod Sci. 2020;27:585–591. doi: 10.1007/s43032-019-00058-9 [DOI] [PubMed] [Google Scholar]
  • 88.Chen B, Zhao Q, Guan L, et al. Long non-coding RNA NNT-AS1 sponges miR-424/E2F1 to promote the tumorigenesis and cell cycle progression of gastric cancer. J Cell Mol Med. 2018;22:4751–4759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Wang RP, Jiang J, Jiang T, Wang Y, Chen LX. Increased long noncoding RNA LINC00511 is correlated with poor prognosis and contributes to cell proliferation and metastasis by modulating miR-424 in hepatocellular carcinoma. Eur Rev Med Pharmacol Sci. 2019;23:3291–3301. [DOI] [PubMed] [Google Scholar]
  • 90.Li D, Tang X, Li M, Zheng Y. Long noncoding RNA DLX6-AS1 promotes liver cancer by increasing the expression of WEE1 via targeting miR-424-5p. J Cell Biochem. 2019;120:12290–12299. doi: 10.1002/jcb.28493 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Wang D, Hu Y. Long non-coding RNA PVT1 competitively binds microRNA-424-5p to regulate CARM1 in radiosensitivity of non-small-cell lung cancer. Mol Ther Nucleic Acids. 2019;16:130–140. doi: 10.1016/j.omtn.2018.12.006 [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
  • 92.Li Y, Zhao L, Zhao P, Liu Z. Long non-coding RNA LINC00641 suppresses non-small-cell lung cancer by sponging miR-424-5p to upregulate PLSCR4. Cancer Biomark. 2019;26:79–91. doi: 10.3233/CBM-190142 [DOI] [PubMed] [Google Scholar]
  • 93.Ding J, Zhang L, Chen S, Cao H, Xu C, Wang X. lncRNA CCAT2 enhanced resistance of glioma cells against chemodrugs by disturbing the normal function of miR-424. Onco Targets Ther. 2020;13:1431–1445. doi: 10.2147/OTT.S227831 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Sun S-L, Shu Y-G, Tao M-Y. LncRNA CCAT2 promotes angiogenesis in glioma through activation of VEGFA signalling by sponging miR-424. Mol Cell Biochem. 2020;468:69–82. doi: 10.1007/s11010-020-03712-y [DOI] [PubMed] [Google Scholar]
  • 95.Han Y, Li X, He F, et al. Knockdown of lncRNA PVT1 inhibits glioma progression by regulating miR-424 expression. Oncol Res. 2019;27:681–690. doi: 10.3727/096504018X15424939990246 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Zhou K, Li S, Du G, et al. LncRNA XIST depletion prevents cancer progression in invasive pituitary neuroendocrine tumor by inhibiting bFGF via upregulation of microRNA-424-5p. Onco Targets Ther. 2019;12:7095–7109. doi: 10.2147/OTT.S208329 [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
  • 97.Li MM, Dong CX, Sun B, et al. LncRNA-MALAT1 promotes tumorogenesis of infantile hemangioma by competitively binding miR-424 to stimulate MEKK3/NF-kappaB pathway. Life Sci.. 2019;239:116946. doi: 10.1016/j.lfs.2019.116946 [DOI] [PubMed] [Google Scholar]
  • 98.Zhang J, Liu h, Hou L, et al. Circular RNA_LARP4 inhibits cell proliferation and invasion of gastric cancer by sponging miR-424-5p and regulating LATS1 expression. Mol Cancer. 2017;16:151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Hu Y, Gu J, Shen H, et al. Circular RNA LARP4 correlates with decreased Enneking stage, better histological response, and prolonged survival profiles, and it elevates chemosensitivity to cisplatin and doxorubicin via sponging microRNA-424 in osteosarcoma. J Clin Lab Anal. 2020;34:e23045. doi: 10.1002/jcla.23045 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Zhao B, Tumaneng K, Guan KL. The Hippo pathway in organ size control, tissue regeneration and stem cell self-renewal. Nat Cell Biol. 2011;13(8):877–883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Zheng Y, Pan d. The Hippo Signaling Pathway in Development and Disease. Dev Cell. J Clin Lab Anal. 2019;50(3):264–282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Olsen JV, Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. Cell. 2006;127(3):635–648. [DOI] [PubMed] [Google Scholar]
  • 103.Wang X, Zhang S, MacLennan GT, et al. Epidermal growth factor receptor protein expression and gene amplification in small cell carcinoma of the urinary bladder. Clinical Cancer Research. 2007;13(3):953–957. [DOI] [PubMed] [Google Scholar]
  • 104.Wang X, Zhang S, MacLennan GT, et al. Epidermal growth factor receptor protein expression and gene amplification in the chemorefractory metastatic embryonal carcinoma. Modern Pathology. 2009;22(1):7–12. [DOI] [PubMed] [Google Scholar]

Articles from OncoTargets and therapy are provided here courtesy of Dove Press

RESOURCES