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. 2022 Apr 6;10:784968. doi: 10.3389/fcell.2022.784968

miR-874: An Important Regulator in Human Diseases

Qiudan Zhang 1,2, Chenming Zhong 2, Qianqian Yan 2, Ling-hui Zeng 1, Wei Gao 1,*, Shiwei Duan 1,2,*
PMCID: PMC9019486  PMID: 35465322

Abstract

miR-874 is located at 5q31.2, which is frequently deleted in cancer. miR-874 is downregulated in 22 types of cancers and aberrantly expressed in 18 types of non-cancer diseases. The dysfunction of miR-874 is not only closely related to the diagnosis and prognosis of tumor patients but also plays an important role in the efficacy of tumor chemotherapy drugs. miR-874 participates in the ceRNA network of long non-coding RNAs or circular RNAs, which is closely related to the occurrence and development of cancer and other non-cancer diseases. In addition, miR-874 is also involved in the regulation of multiple signaling pathways, including the Wnt/β-catenin signaling pathway, Hippo signaling pathway, PI3K/AKT signaling pathway, JAK/STAT signaling pathway, and Hedgehog signaling pathway. This review summarizes the molecular functions of miR-874 in the biological processes of tumor cell survival, apoptosis, differentiation, and tumorigenesis, and reveal the value of miR-874 as a cancer biomarker in tumor diagnosis and prognosis. Future work is necessary to explore the potential clinical application of miR-874 in chemotherapy resistance.

Keywords: miR-874, cancer, tumor suppressor, non-cancer, diagnosis, prognosis, ceRNA, pathway

Background

MicroRNA (miRNA) is a short RNA of 19–25 nucleotides in length that can regulate the post-transcriptional silencing of target genes. A single miRNA can target hundreds of mRNAs, thereby affecting the signal transduction of multiple pathways (Lu and Rothenberg, 2018). miRNA expression profiling shows that abnormal miRNA expression is related to the occurrence and progression of tumors and the response to anticancer drugs (Iorio and Croce, 2017). In addition, almost all developmental, physiological, and disease-related processes seem to be linked to miRNAs (Sun and Lai, 2013).

microRNA-874 (miR-874) is a new anti-cancer miRNA (Zhang et al., 2018b). It was originally obtained by sequencing a small RNA library (Song et al., 2016) and was first characterized in normal human cervical tissue samples (Xia et al., 2018). miR-874 is located on chromosome 5q31.2 that is often deleted in cancer (Zhang et al., 2018b). There are many target genes of miR-874 (Figure 1). By inhibiting the expression of these target genes, miR-874 is widely involved in cell proliferation, apoptosis, invasion, migration, cell cycle, epithelial-mesenchymal transition (EMT), and other cellular processes.

FIGURE 1.

FIGURE 1

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Dysregulation of miR-874 in human cancer and non-cancer diseases. HCC, Hepatocellular carcinoma; PDAC, Pancreatic ductal adenocarcinoma; NSCLC, Non-small cell lung cancer; OS, Osteosarcoma; EOC, Epithelial ovarian cancer; CC, Cervical cancer; TNBC, Triple negative breast cancer; r BC, Breast cancer; CRC, Colorectal cancer; ESCC, Esophageal squamous cell Squamous cell carcinoma; MSCC, Maxillary sinus squamous cell carcinoma; RB, Retinoblastoma; GC, Gastric cancer; RMS, Rhabdomyosarcoma; PTC, Papillary thyroid carcinoma; MM, myeloma; AML, acute myeloid leukemia; HNSCC, head and neck squamous cell carcinoma.

Since there is no comprehensive introduction of miR-874, this work summarizes the abnormal expression of miR-874 in cancer and non-cancerous diseases, and outlines the molecular mechanisms between it and protein-coding genes and non-coding RNAs.

The Aberrant Expression of miR-874 in Human Diseases

As shown in Table 1, miR-874 is downregulated in at least 22 human malignancies, such as colorectal cancer (CRC) (Huang et al., 2020a; Yu et al., 2020; Que et al., 2017; Zhao and Dong, 2016; Han et al., 2016; Wang et al., 2021; Zhang et al., 2021c), gastric cancer (GC) (Huang et al., 2018; Sun et al., 2020; Yuan et al., 2020; Liu et al., 2017; Zhang et al., 2015; Jiang et al., 2014), hepatocellular carcinoma (HCC) (Zhang et al., 2018b; Jiang et al., 2017; Leong et al., 2017; Song et al., 2016), esophageal squamous cell carcinoma (ESCC) (Yuan et al., 2018), pancreatic ductal adenocarcinoma (PDAC) (Diao et al., 2018), non-small cell lung cancer (NSCLC) (Bu et al., 2020; Yang et al., 2017; Ahmad et al., 2015; Kesanakurti et al., 2013; Wang et al., 2020b), osteosarcoma (OS) (Tang et al., 2018; Liu et al., 2020; Dong et al., 2016; Ghosh et al., 2017), epithelial ovarian cancer (EOC) (Xia et al., 2018) cervical cancer (CC) (Liao et al., 2018; Liu et al., 2021a), retinoblastoma (RB) (Zhang et al., 2018a; Wang et al., 2020a), prostate cancer (PCa) (Pashaei et al., 2017) maxillary sinus squamous cell carcinoma (MSCC) (Nohata et al., 2011), breast cancer (BC) (Li et al., 2020; Zhang et al., 2017; Wang et al., 2014), triple-negative breast cancer (TNBC) (Wu et al., 2020), rhabdomyosarcoma (RMS) (Shang et al., 2019), papillary thyroid carcinoma (PTC) (Ding et al., 2021), endometrial cancer (Witek et al., 2021), cholangiocarcinoma (Pan et al., 2021), glioma (Li et al., 2021a), myeloma (MM) (Tian et al., 2021), head and neck squamous cell carcinoma (HNSCC) (Nohata et al., 2013) and acute myeloid leukemia (AML) (Zhang et al., 2021a).

TABLE 1.

The role of miR-874 in various cancers.

Cancer Type The expression of miR-874 Effect in vivo Effect in vitro Regulatory mechanism References
CRC downregulation tumor growth↓ proliferation↓, apoptosis↑ circ_0007142/miR-874-3p/GDPD5 Wang et al. (2021)
downregulation tumor growth↓ proliferation↓, migration↓, invasion↓ lncRNA MCF2L-AS1/miRNA-874-3p/FOXM1 Zhang et al. (2021c)
downregulation tumor growth↓ proliferation↓, migration ↓, invasion↓, EMT↓ lncRNA MCF2L-AS1/miRNA-874-3p/CCNE1 Huang et al. (2020a)
downregulation tumor growth↓ proliferation↓, apoptosis↑ circ_0005576/miRNA-874-3p/CDK8/Wnt/β-catenin Yu et al. (2020)
downregulation tumor growth↓ chemosensitivity↓ miR-874-3p/YAP1, TAZ/Hippo signaling Que et al. (2017)
downregulation tumor growth↓ cell growth↓, apoptosis↑ miR-874-3p/STAT3 Zhao and Dong, (2016)
downregulation tumor growth↓ proliferation↓, colony formation↓, apoptosis↑, chemosensitivity↓ miR-874-3p/XIAP/CASP3, CASP7, CASP9/5-FU Han et al. (2016)
GC downregulation prognosis↑ autophagy↓, chemosensitivity↓ miR-874-3p/ATG16L1 Huang et al. (2018)
downregulation tumor growth↓ proliferation↓, apoptosis↑ miR-874-3p/SPAG9 Sun et al. (2020)
downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, EMT↓ IIA (TSN)/miR-874-3p/HMGB2/Wnt/β-catenin Yuan et al. (2020)
downregulation tumor growth ↓ migration ↓, invasion↓, proliferation↓, angiogenesis↓ miR-874/ARHGEF25 Huang et al. (2018)
downregulation tumor growth↓ angiogenesis↓ tube formation↓, proliferation↓, migration↓, invasion↓ miR-874-3p/STAT3/VEGFA Zhang et al. (2015)
downregulation tumor growth↓ proliferation↓, colony formation↓, migration↓, invasion↓ miR-874-3p/CASP3, AQP3 Jiang et al. (2014)
HCC downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, EMT↓ miR-874/OPRD1/EGFR/MAPK1 caggca Zhang et al. (2018b)
downregulation tumor growth↓ migration↓, invasion↓, EMT↓ miR-874-3p/SOX12 Jiang et al. (2017)
downregulation tumour growth↓ cell growth ↓, colony formation↓, apoptosis↑ miR-874-3p/PPNE1 Leong et al. (2017)
downregulation tumor growth ↓ proliferation↓, invasion↓ miR-874-3p/MAGEC2 Song et al. (2016)
ESCC downregulation tumor growth↓ prognosis↑ proliferation↓, migration↓, invasion↓ miR-874-3p/STAT3 Yuan et al. (2018)
PDAC downregulation tumor growth↓ proliferation↓, migration↓, invasion↓ miR-874-3p/PAX6 Diao et al. (2018)
NSCLC downregulation tumor growth↓ xenograft growth↓ proliferation↓, migration↓, invasion↓, EMT↓ miR-874-3p/AQP1 Wang et al. (2020b)
tumor growth↓ proliferation↓, migration↓, invasion↓ MIR210HG/miRNA-874-3p/STAT3 Bu et al. (2020)
downregulation tumor growth↓ proliferation ↓, invasion↓, apoptosis↑ lncRNA XLOC_008466/miR-874-3p/MMP2, XIAP Yang et al. (2017)
downregulation invasion↓ CDF/miR-874/MMP2 25901198 Ahmad et al. (2015)
downregulation tumor growth ↓ invasion↓, de-differentiation↑, migration↓ miR-874-3p/MMP2, PLAU Kesanakurti et al. (2013)
OS downregulation tumor growth↓ proliferation↓, migration↓, invasion↓ miR-874-3p/CDK9 Tang et al. (2018)
downregulation tumor growth↓ proliferation↓, migration↓, invasion↓ miR-874-3p/RGS4 Liu et al. (2020)
downregulation tumor growth ↓ metastasis ↓ proliferation↓, apoptosis↑, migration↓, invasion↓ miR-874-3p/E2F3 Dong et al. (2016)
downregulation tumor growth↓ invasion↓, migration↓ lncRNA XLOC_008466/miR-874-3p/CCNE1 Ghosh et al. (2017)
EOC downregulation tumor growth↓ colony formation↓, apoptosis↑, paclitaxel sensitivity↑, migration↓, invasion↓, chemoresistance↓ miR-874-3p, miR-874-5p/SIK2 Xia et al. (2018)
CC downregulation tumor growth↓ proliferation↓, migration↓, invasion↓ Liu et al. (2021a)
downregulation tumor growth↓ proliferation↓, apoptosis↑, migration↓, invasion↓ miR-874/ETS1 Liao et al. (2018)
PCa downregulation Pashaei et al. (2017)
TNBC downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, EMT↓ lncRNA DANCR/miRNA-874-3p/SOX2 Wu et al. (2020)
BC downregulation tumor growth↓ Zhang et al. (2017)
downregulation tumor growth↓ proliferation↓, apoptosis↑, cell circle↓ miR-874/CDK9 Wang et al. (2014)
HNSCC downregulation tumor growth↓ proliferation↓, cell cycle↓, apoptosis↑ miR-874-3p/HDAC1 Nohata et al. (2013)
MSCC downregulation tumor growth↓ proliferation↓, invasion↓ miR-874-3p/PPP1CA Nohata et al. (2011)
RB downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, apoptosis↑ miR-874-3p/MTDH Zhang et al. (2018a)
downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, EMT↓ lncRNA TP73-AS1/miRNA-874-3p/TFAP2B/Wnt/β-catenin Wang et al. (2020a)
RMS downregulation tumor growth↓ migration↓, invasion↓, apoptosis↑ miR-874-3p/GEFT Shang et al. (2019)
Glioma downregulation tumor growth↓ proliferation↓, migration ↓, invasion↓ Li et al. (2021a)
Cholangiocarcinoma downregulation tumor growth↓ migration↓, invasion↓, EMT↓ miR-874-3p/CCNE1/NF-κB signailing pathway Pan et al. (2021)
MM downregulation tumor growth↓ viability↓, proliferation↓, autophagy↓, apoptosis↑ circ_0003489/miR-874-3p/HDAC1 Tian et al. (2021)
PTC downregulation tumor growth↓ proliferation↓, migration↓, invasion↓, apoptosis↑, EMT↓ miR-874-3p/FAM84A/Wnt/β-catenin Ding et al. (2021)
Endometrial cancer downregulation tumor growth↓ cell cycle↓ Witek et al. (2021)
AML downregulation tumor growth↓ autophagy↑ lncRNA DANCR/miR-874-3p/ATG16L1 Zhang et al. (2021a)
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HCC, Hepatocellular carcinoma; PDAC, Pancreatic ductal adenocarcinoma; NSCLC, Non-small cell lung cancer; OS, Osteosarcoma; EOC, Epithelial ovarian cancer; CC, Cervical cancer; PCa, Prostate cancer; TNBC, Triple negative breast cancer; BC, Breast cancer; CRC, Colorectal cancer; ESCC, Esophageal squamous cell Squamous cell carcinoma; MSCC, Maxillary sinus squamous cell carcinoma; RB, Retinoblastoma; GC, Gastric cancer; RMS, Rhabdomyosarcoma; PTC, Papillary thyroid carcinoma; MM, myeloma; AML, acute myeloid leukemia; HNSCC, head and neck squamous cell carcinoma; CDF, Novel difluorobenzylidene analogue of curcumin; TSN, Tanshinone IIA; EMT, epithelial-mesenchymal transition.

HNSCC is the sixth most common cancer in the world (Nohata et al., 2013). The expression of miR-874-3p is reduced in HNSCC, and miR-874-3p can be upregulated after 5-Aza-dC treatment, indicating that the downregulation of miR-874-3p in HNSCC may be due to the methylation of its upstream CpG island (Nohata et al., 2013). Histone deacetylase 1 (HDAC1) belongs to the HDAC family. HDAC removes acetyl groups from histones and other nuclear proteins that induce chromatin condensation and transcriptional inhibition. HDAC plays an important role in the abnormal epigenetic changes associated with human cancer (Witt et al., 2009). In HNSCC, miR-874-3p can directly target HDAC1, significantly inhibit cell proliferation, and induce cell cycle arrest and apoptosis (Nohata et al., 2013).

Also, miR-874 plays an important role in non-cancer diseases. Low expression of miR-874 is associated with the risk of ischemic stroke (IS) (Jiang et al., 2019; Xie et al., 2020; Zhang et al., 2021b), ischemic heart disease (IHD) (Chen et al., 2019), cardiomyocyte necrosis (Wang et al., 2013), diabetic erectile dysfunction (DMED) (Huo et al., 2020), diabetic nephropathy (DN) (Yao et al., 2018), sepsis (Fang et al., 2018), osteoporosis (Lin et al., 2018), Parkinson’s disease (PD) (Zhao et al., 2020), acute myocardial infarction (AMI) (Yan et al., 2017), intestinal barrier dysfunction (Su et al., 2016), periodontal tissue repair and regeneration (Huang et al., 2020b), idiopathic short stature (ISS) (Liu et al., 2021b), intervertebral disc degeneration (IDD) (Song et al., 2021a), pneumonia (Yang et al., 2021), and human periodontal ligament fibroblasts (Song et al., 2021b) (Table 2).

TABLE 2.

The role of miR-874 in human non-cancer diseases.

Non-cancer Type The expression of miR-874 Effect in vivo Effect in vitro Regulatory mechanism References
Ischemic stroke downregulation cerebral I/R injury↓ proliferation↑, apoptosis↓ miR-874-3p/BMF, BCL2L13 Jiang et al. (2019)
downregulation apoptosis↑ MIAT/miR-874-3p/IL1B Zhang et al. (2021b)
downregulation angiogenesis↑, inflammatory factor release↓ apoptosis↓ miR-874-3p/CXCL12/Wnt/β-catenin Xie et al. (2020)
Ischemic heart disease downregulation cardiac function↓ apoptosis↑ miR-874-3p/STAT3 Chen et al. (2019)
Cardiomyocyte necrosis downregulation apoptosis↑, necrosis↑ FOXO3/miR-874/CASP8 Wang et al. (2013)
Diabetic nephropathy downregulation inflammatory cytokines expression↓ proliferation↑, apoptosis↓ miR-874-3p/TLR4 Yao et al. (2018)
Diabetic erectile dysfunction downregulation erectile dysfunction↓ apoptosis↓ miR-874-3p/NUPR1/DDIT3 Huo et al. (2020)
Sepsis downregulation sepsis↓ lncRNA H19/miR-874/AQP1 Fang et al. (2018)
Periodontal tissue repair and regeneration lncRNA FER1L4/miR-874-3p/VEGFA Huang et al. (2020b)
Osteoporosis downregulation proliferation↑, apoptosis↓, osteoblasts in S phase↑, ALP activity↑, calcium nodules↑ miR-874-3p/SUFU/Hedgehog pathway Lin et al. (2018)
Parkinson’s disease downregulation MPP + -induced neuronal injury↓ lncRNA HOTAIR/miR-874-5p/ATG10 Zhao et al. (2020)
Bone porosis upregulation osteoblast differentiation↑, mineralization↑ miR-874-3p/HDAC1/RUNX2 Kushwaha et al. (2016)
Acute myocardial infarction downregulation apoptosis↑ miR-874-3p/GZMB Yan et al. (2017)
Intestinal barrier dysfunction downregulation lncRNA H19/miR-874-3p/AQP3 Su et al. (2016)
Intervertebral disc degeneration downregulation miR-874-3p/MMP2/MMP3 Song et al. (2021a)
upregulation proliferation↓, apoptosis↑ circ_0040039/miR-874-3p↑/ESR1 Li et al. (2021b)
Polycystic ovary syndrome and granulosa cell apoptosis upregulation apoptosis↑ miR-874-3p/HDAC1/p53 axis Wei et al. (2021)
Idiopathic short stature downregulation proliferation↓, cell circle↓ circANAPC2/miR-874-3p/Smad3 Liu et al. (2021b)
Human periodontal ligament fibroblasts downregulation differentiation↑ miR-874-3p/WNT3A, WNT/β-catenin Song et al. (2021b)
Pneumonia downregulation apoptosis↓ miR-874-3p/EGR3/NF-κB Yang et al. (2021)
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I/R, ischaemia/reperfusion; ALP, Alkaline phosphatase.

Highly expressed miR-874-3p is associated with the risk of bone porous (Kushwaha et al., 2016) and polycystic ovary syndrome (PCOS) (Wei et al., 2021), IDD (Li et al., 2021b). miR-874-3p in maternal osteoblasts increased 4–6 times during the child’s weaning period. Increasing the expression of miR-874-3p could enhance bone formation and restore the mother’s bone quality after pregnancy and lactation (Kushwaha et al., 2016). In granulosa cells, testosterone promotes p53 acetylation and expression by upregulating the expression of miR-874-3p and induces granulosa cell apoptosis (Wei et al., 2021), thereby promoting the occurrence and development of PCOS (Wei et al., 2021) (Table 2).

However, the results of the association between miR-874-3p expression and IDD are divergent. The expression level of miR-874-3p in the NP tissues of IDD patients was significantly reduced, thereby upregulating the expression of MMP2 and MMP3, eventually leading to the occurrence of IDD (Song et al., 2021a). In nucleus pulposus cells (NPCs), circ_0040039 can increase the stability of miR-874-3p and upregulate the miR-874-3p/ESR1 pathway to aggravate IDD (Li et al., 2021b). The different effects of miR-874-3p in IDD may be related to the tested sample types. It is worth noting that the sample size of IDD-related studies is small, and there is a lack of follow-up experiments to further explore the in vivo function of miR-874-3p. In the future, more samples and in vivo experiments are needed to confirm the mechanism of miR-874-3p in IDD.

The Effect of miR-874 on Prognosis and Chemoresistance

In patients of HCC, OS, or RMS, decreased expression of miR-874 is associated with tumor size, vascular infiltration, lymph node metastasis, tumor-node-metastasis (TNM) staging, clinical staging, and tumor differentiation (Dong et al., 2016; Zhang et al., 2018b; Shang et al., 2019). Subsequent cell function experiments revealed the tumor suppressor effects of miR-874, including inhibition of proliferation, invasion, metastasis, and promotion of apoptosis (Diao et al., 2018) (Table 3).

TABLE 3.

The contribution of miR-874 to the treatment, clinicopathological characteristics, and prognosis in cancer.

Cancer Type Sample size Expression pattern of miR-874 Radiosensitivity/Chemoresistance Clinicopathological characteristics/Prognostic value References
GC 50 paired tissues downregulation DDP, VCR, 5-FU prognostic factor of OS Huang et al. (2018)
CRC 32 paired tissues downregulation 5-FU prognostic factor of OS correlated with lymph node metastasis and TNM stage Han et al. (2016)
20 paired tissues downregulation 5-FU Que et al. (2017)
HCC 120 paired tissues downregulation prognostic factor of OS and RFS correlated with tumour size, vascular invasion, TNM stage, tumour differentiation and inferior patient outcomes Zhang et al. (2018b)
ESCC 121 paired tissues downregulation independent prognostic factor of OS Yuan et al. (2018)
NSCLC 32 paired tissues downregulation Radiosensitivity, chemoresistance Bu et al. (2020)
49 paired tissues downregulation prognostic factor of OS Li et al. (2020)
PDAC 29 paired tissues downregulation correlated with TNM stage, tumor size, and lymph node metastasis Diao et al. (2018)
OS 40 paired tissues downregulation correlated with TNM stage, tumor size, and lymph node metastasis Dong et al. (2016)
EOC 20 paired tissues downregulation chemoresistance Xia et al. (2018)
CC 49 paired tissues downregulation prognostic factor of OS correlated with tumour differentiation and lymph node metastasis Liao et al. (2018)
BC 26 paired tissues downregulation correlated with pathological differentiation and tumor size Wang et al. (2014)
47 paired tissues downregulation prognostic factor of OS correlated with pathological differentiation, TNM staging and lymph node metastasis Zhang et al. (2017)
RB 26 paired tissues downregulation correlated with tumor stage Zhang et al. (2018a)
50 paired tissues downregulation prognostic factor of OS correlated with different clinicopathological stage Wang et al. (2020a)
RMS 10 paired tissues downregulation correlated with the advanced clinical stage, lymph node metastasis, and distant metastasis of RMS Shang et al. (2019)
AML HL60, U937, and KG1a downregulation Ara-C Zhang et al. (2021a)
MM MM1.R downregulation BTZ Tian et al. (2021)
Glioma 105 paired tissues downregulation independent prognostic factor for OS correlated with tumor size, KPS score, and TNM stage Li et al. (2021a)
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GC, Gastric cancer; CRC, Colorectal cancer; HCC, Hepatocellular carcinoma; ESCC, Esophageal squamous cell Squamous cell carcinoma; NSCLC, Non-small cell lung cancer; PDAC, Pancreatic ductal adenocarcinoma; OS, Osteosarcoma; EOC, Epithelial ovarian cancer; CC, Cervical cancer; r BC, Breast cancer; RB, Retinoblastoma; RMS, Rhabdomyosarcoma; MM, myeloma; AML, acute myeloid leukemia; TNM, Tumor node metastasis; OS, Overall survival rate; RFS, Recurrence free survival.

As shown in Table 3, compared with cancer patients with high miR-874 expression, patients with low miR-874 expression have a significantly worse prognosis. These cancers include GC (Huang et al., 2018), CRC (Han et al., 2016), HCC (Zhang et al., 2018b), ESCC (Yuan et al., 2018), NSCLC (Li et al., 2020), CC (Liao et al., 2018), BC (Zhang et al., 2017), RB (Wang et al., 2020a), and glioma (45).

In GC, CRC, NSCLC, and EOC, miR-874 can reduce the drug resistance of cancer cells (Huang et al., 2018; Han et al., 2016; Que et al., 2017; Bu et al., 2020; Xia et al., 2018). Among them, the upregulation of miR-874 expression in CRC cells can increase the sensitivity to 5-FU (Han et al., 2016; Que et al., 2017). The overexpression of miR-874 significantly enhanced the sensitivity of GC cells to DDP, VCR, and 5-FU (Huang et al., 2018). The MIR210HG/miR-874/STAT3 axis plays a carcinogenic regulatory role in the radiosensitivity and drug resistance of NSCLC (Bu et al., 2020). miR-874-3p and miR-874-5p can enhance the chemical sensitivity of EOC cells (Xia et al., 2018).

Cancer cells use autophagy to provide energy and develop resistance to anti-cancer drugs; therefore, inhibiting autophagy may promote cancer cell death and help overcome drug resistance (Levy et al., 2017). Autophagy involved in miR-874-3p is an important mechanism for regulating chemotherapy resistance in AML (Zhang et al., 2021a). In AML, the DANCR/miR-874-3p/ATG16L1 axis can promote autophagy, thereby enhancing the resistance of human AML cells to Ara-C (Zhang et al., 2021a). In addition, knocking out circ_0003489 can upregulate miR-874-3p and inhibit HDAC1, thereby prompting MM cells to switch from autophagy to apoptosis, and reducing the growth of MM cells (Tian et al., 2021).

The above findings indicate that miR-874 can be developed as a new diagnostic and prognositc biomarker for patients with the above cancer types and suggest a potential value of miR-874 in cancer drug resistance.

The ceRNA Network Centered on miR-874

Non-coding RNA can regulate gene expression, thereby affecting cell proliferation, survival, and migration, and is related to genome stability and malignant transformation of inflammatory cells (Zhang et al., 2021a). There are interactions between non-coding RNAs. For example, lncRNAs and circRNAs can be used as ceRNAs to sponge miRNAs (Zhang et al., 2021a). The ceRNA network centered on miR-874 is involved with at least 10 lncRNAs or 12 circRNAs. The dysfunction of miR-874 is closely related to the occurrence and development of tumors and other diseases (Figure 2).

FIGURE 2.

FIGURE 2

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The ceRNA mechanisms of miR-874 in cancer and other non-cancer diseases.

In TNBC, lncRNA DANCR acts as a ceRNA for miR-874-3p, thereby regulating the derepression of SOX2 and promoting the EMT in TNBC (Wu et al., 2020). In CRC, the MCF2LAS1/miR-874-3p/FOXM1 axis (Liao et al., 2018) and MCF2LAS1/miR-874-3p/CCNE1 axis (Huang et al., 2020a) can promote cancer cell apoptosis, inhibit cancer cell proliferation, invasion, migration and EMT process. Also, the circ_0005576/miR-874/CDK8 axis can promote the malignant progression of CRC (Yu et al., 2020). In CRC cells, circ_0007142 can regulate the level of GDPD5 by sponging miR-874-3p (12). Knock-down of circ_0007142 can induce ferroptosis through the circ_0007142/miR-874-3p/GDPD5 axis, thereby increasing the effectiveness of chemotherapy or radiotherapy and inhibiting the malignant progression of CRC (Wang et al., 2021). In RB, the expression of lncRNA TP73-AS1 is upregulated, and the downregulated TP73-AS1/miR-874-3p/TFAP2B axis can inhibit the Wnt/β-catenin signaling pathway, thereby inhibiting tumor progression (Wang et al., 2020a). In NSCLC, the miR210HG/miR-874-3p/STAT3 axis plays a role in the progression of NSCLC cells (Bu et al., 2020). Besides, XLOC_008466, as the ceRNA of miR-874-3p, can increase the expression of MMP2 and XIAP and affect NSCLC cell proliferation, apoptosis, and invasion (Yang et al., 2017; Bu et al., 2020). In OS, the downregulated lncRNA XLOC_008466/miR-874-3p/CCNE1 axis can also inhibit tumor growth (Ghosh et al., 2017). The expression of lncRNA DCST1-AS1 increases in cervical cancer tissues and cells, and inhibition of DCST1-AS1 can increase the expression of miR-874-3p, thereby inhibiting the proliferation, migration and invasion of cervical cancer cells (Liu et al., 2021a). In PTC, miR-874-3p can inhibit FAM84A and exert carcinogenic effects through the Wnt/β-catenin signal transduction (Ding et al., 2021). LncRNA DANCR is a promising tumor-related lncRNA that can enhance cancer cell proliferation, stemness, invasion, and metastasis (Zhang et al., 2021a). In AML, DANCR regulates autophagy by promoting the miR-874-3p/ATG16L1 axis, thereby reducing Ara-C resistance in human AML cells (Zhang et al., 2021a). BTZ is a first-class proteasome inhibitor approved by the FDA for the treatment of newly diagnosed and relapsed MM patients. In MM, the circ_0003489/miR-874-3p/HDAC1 axis plays a crucial role in controlling the balance of autophagy and apoptosis in MM cells. Downregulation of circ_0003489 can increase the inhibition of miR-874-3p on HDAC1, and improve the efficacy of BTZ in the treatment of MM (Tian et al., 2021).

Besides, we found that the ceRNA network of miR-874 also plays an important role in non-cancer diseases. The H19/miR-874/AQP1 axis can help restore inflammatory response to lipopolysaccharide (LPS) and inflammation associated with sepsis-induced myocardial dysfunction (Fang et al., 2018). Also, the H19/miR-874/AQP3 axis plays an important role in maintaining the intestinal barrier function (Su et al., 2016). During the continuous osteogenic differentiation of periodontal ligament stromal cells (PDLSCs), the FER1L4/miR-874-3p/VEGFA axis can positively regulate the osteogenic differentiation of PDLSCs (Huang et al., 2020b). In PD, the HOTAIR/miR-874-5p/ATG10 axis can promote MPP+-induced neuronal damage (Zhao et al., 2020). miR-874-3p can reduce the levels of TNF-α, IL-1, IL-6, and IL-8, increase the level of IL-10, reduce neuronal apoptosis, and significantly inhibit brain inflammation in the IS model mice. LncRNA MIAT can sponge miR-874-3p to increase the risk of IS (Zhang et al., 2021b). In addition, circANAPC2 is upregulated in ISS patients, and it can inhibit the proliferation, hypertrophy, and endochondral ossification of chondrocytes through the circANAPC2/miR-874-3p/SMAD3 axis in vitro (Liu et al., 2021b).

It is worth noting that circRNA-mediated regulation of miRNA expression consists of two modes (Piwecka et al., 2017). One is the classical sponge mechanism, in which circRNA inhibits or does not affect miRNA expression. The other is a stabilization mechanism in which circRNAs increase the expression of miRNAs. In IDD, circ_0040039 can stabilize miR-874-3p and inhibit the expression level of ESR1, thereby promoting the apoptosis of the NPCs and inhibiting the growth of NPCs (Li et al., 2021b).

The miR-874 Related Signaling Pathways

The target genes of miR-874 are involved in at least five classical signaling pathways, including the Wnt/β-catenin pathway [TFAP2B (Wang et al., 2020a), CDK8 (Yu et al., 2020), HMGB2 (Yuan et al., 2020), CXCL12 (Xie et al., 2020), and FAM84A (Ding et al., 2021)], the Hippo pathway [YAP1 and TAZ (Que et al., 2017)], the PI3K/AKT pathway [AQP3 (Li et al., 2020)], the JAK/STAT pathway [STAT3 (Zhang et al., 2015; Li et al., 2020; Zhao and Dong, 2016; Bu et al., 2020; Yuan et al., 2018; Shang et al., 2019)] and the Hedgehog signaling pathway [SUFU (Lin et al., 2018)] (Figure 3).

FIGURE 3.

FIGURE 3

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miR-874 regulate many biological processes within the cell. The target genes of miR-874 are involved in at least five classical signaling pathways, including the Wnt/β-catenin signaling pathway, P13/AKT signaling pathway, Hippo signaling pathway, JAK/STAT signaling pathway, and Hedgehog signaling pathway. EMT, epithelial-mesenchymal transition.

The Wnt/β-Catenin Signaling Pathway

The close relationship between miR-874 and Wnt/β-catenin signaling pathway is of great significance not only for tumor diseases but also for IS (Figure 3). Wnt/β-catenin signaling pathway plays a key role in regulating cell growth, cell development, and normal stem cell differentiation. Constitutive activation of the Wnt/β-catenin signaling pathway has been found in many human cancers (Yao et al., 2011). In RB tissues and cells, the TP73-AS1/miR-874-3p/TFAP2B axis can activate the Wnt/β-catenin signaling pathway and enhance the expression of downstream tumor-related factors TCF4, BCL2, CCND1, and MYC (Wang et al., 2020a).

Abnormal activation of the Wnt/β-catenin signaling pathway occurs in almost all CRC (Wang et al., 2020a). In CRC, the circ_0005576/miR-874-3p/CDK8 axis can cause the abnormal activation of the Wnt/β-catenin signaling pathway and the proliferation of CRC cells (Yu et al., 2020). In GC cell lines the downregulation of the miR-874-3p/HMGB2 axis can upregulate the expression of β-catenin, CCND1, and MYC, which shows that the abnormal activation Wnt/β-catenin signaling pathway may be regulated by the miR-874-3p/HMGB2 axis in GC (Yuan et al., 2020).

The expression of serum CXCL12 in patients with IS was higher than that in healthy controls. CXCL12 can act as a ligand for CXC motif chemokine receptor 4 (CXCR4) and is a downstream target gene of miR-874-3p (Xie et al., 2020). In mice with IS, the Wnt/β-catenin signaling pathway is inhibited, and downregulation of CXCL12 can activate the Wnt/β-catenin signaling pathway, thereby promoting angiogenesis and inhibiting the brain tissue apoptosis in mice with IS (Xie et al., 2020). This suggests that the miR-874-3p/CXCL12 axis can activate the Wnt/β-catenin signaling pathway, which provides a new hint for the treatment of IS (Xie et al., 2020).

In PTC, FAM84A can activate EMT and the Wnt/β-catenin signaling pathway, thereby inducing tumorigenesis of thyroid cancer (Ding et al., 2021). miR-874-3p can target the 3′UTR of FAM84A, thereby reducing the expression of FAM84A. Attenuation of miR-874-3p/FAM84A/Wnt/β-catenin axis can inhibit PTC tumor progression (Ding et al., 2021).

In addition, miR-874-3p/WNT/β-catenin axis can inhibit the osteogenic differentiation of hPDLF. During osteogenic differentiation of hPDLF, the downregulation of miR-874-3p corresponds to the increase in WNT3A expression, while overexpression of miR-874-3p can inhibit WNT3A expression, thereby upregulating the expression of the β-catenin protein (Song et al., 2021b).

The Hippo Signaling Pathway

The Hippo signaling pathway can regulate cell growth, differentiation, aging, contact inhibition, and other biological processes, and plays an important role in maintaining cell growth and maintaining the stability of apoptosis balance (Que et al., 2017). YAP1 and TAZ are downstream transcriptional effectors of the Hippo signaling pathway, which can promote cell growth, invasion, and migration (Que et al., 2017). In CRC cells, the ectopic expression of miR-874-3p can inhibit the expression of YAP1 and TAZ, and by downregulating the expression of BCL2 and BCL2L1, increasing the activity of CASP9 and CASP3, thereby promoting 5-FU-induced apoptosis (Que et al., 2017). Downregulation of miR-874-3p can inactivate the Hippo signaling pathway, thereby increasing the resistance of cells to 5-FU chemotherapy (Que et al., 2017) (Figure3).

The PI3K/AKT Signaling Pathway

The PI3K/AKT signaling pathway is downstream of many growth factor receptors. It promotes the proliferation and malignant transformation of tumor cells and inhibits tumor cell apoptosis through the phosphorylation of PI3K and AKT proteins (Lu et al., 2019). Downregulation of miR-874 in NSCLC tissues and cell lines can increase the expression of its target gene AQP3, promote p-PI3K and p-AKT phosphorylation, and activate the PI3K/AKT signaling pathway (Wang et al., 2020b). The above implies that miR-874 deactivates the PI3K/AKT signaling pathway by targeting AQP3 and exerts its tumor suppressor effect (Wang et al., 2020b) (Figure 3).

The JAK/STAT Signaling Pathway

The JAK/STAT signaling pathway includes a family of receptor-associated cytoplasmic tyrosine kinases (JAKs) that phosphorylate tyrosine residues in STAT homologs (Wang et al., 2019). The JAK/STAT signaling pathway plays an inhibitory role in various physiological processes, such as cell development and differentiation (Wang et al., 2019).

miR-874-3p can inhibit the JAK/STAT signaling pathway by inhibiting STAT3 (Figure 3). As an anti-apoptotic factor, STAT3 plays an important role in the regulation of gene expression and mitochondrial electron transport during cellular stress (Wang et al., 2019). miR-874-3p can inhibit STAT3 in several cancers, including GC (Zhang et al., 2015), CRC (Zhao and Dong, 2016), NSCLC (Bu et al., 2020), and ESCC (Yuan et al., 2018). In gastric cancer, constitutive STAT3 activation promotes VEGF-A expression and stimulates tumor angiogenesis. miR-874 can bind to the 3′-UTR of STAT3 and downregulate STAT3 expression, thereby inhibiting angiogenesis (Zhang et al., 2015). In CRC, miR-874 inhibits STAT3 expression by targeting its mRNA 3′UTR, thereby inhibiting cell growth and inducing apoptosis (Zhao and Dong, 2016). In NSCLC cells, miR210HG can downregulate the expression of miR-874, thereby promoting the expression of STAT3 (Bu et al., 2020). In ESCC, the overexpression of miR-874 can inhibit tumor development by targeting STAT3. Besides, in IHD, inhibiting miR-874-3p can activate the JAK2/STAT3 signaling pathway, thereby inhibiting the expression of BAX, upregulating BCL2, reducing cardiomyocyte apoptosis, and ultimately reducing the risk of ischaemia/reperfusion (I/R) damage in mice (Chen et al., 2019).

The Hedgehog Signaling Pathway

The Hedgehog signaling pathway is conservative and it is involved in the proliferation and differentiation of a variety of cells (Lin et al., 2018). SUFU is a negative regulator of the Hedgehog signaling pathway in vertebrates. SUFU can inhibit the GLI transcription factor and induce skeletal dysplasia, osteoarthritis, or chondroma (Lin et al., 2018). By inhibiting SUFU and activating the Hedgehog signaling pathway, miR-874 can promote osteoblast proliferation, increase alkaline phosphatase activity and calcium nodules, and inhibit osteoblast apoptosis (Lin et al., 2018).

Summary

miR-874 is downregulated in many cancers and non-cancer diseases, suggesting that it plays a key role in the physiological and pathological processes of human disease. miR-874 plays an important role in the progression of malignant tumors by regulating a complex ceRNA network. The ceRNA network centered on miR-874 includes at least 10 ncRNAs and 12 protein-coding genes. miR-874 has also been shown to participate in at least 4 important signaling pathways, including the Hippo signaling pathway, Wnt/β-catenin signaling pathway, JAK/STAT signaling pathway, and Hedgehog signaling pathway.

It is worth noting that in the relevant research of IDD, the expression of miR-874-3p is inconsistent. This may be related to the cell state and type, and these differences need to be further verified in large-scale experiments. In IDD, circ_0040039 can enhance miR-874-3p through a stabilization mechanism. In the future, further exploration of miR-874-related stabilization mechanisms will help to understand the ceRNA network of miR-874 and the clinical effectiveness of targeting miR-874.

The abnormal expression of miR-874 is closely related to the clinicopathological characteristics of 15 cancers. Therefore, miR-874 can be used as a potential biomarker for the early prediction of cancer. In addition, in AML and MM, miR-874 participates in the regulation of autophagy-related functions and affects drug resistance of cells, which provides new ideas for overcoming drug resistance. However, the current research of miR-874 is focused on the exploration of the mechanism of its upstream and downstream genes. The potential clinical application of miR-874 in cancer prognosis and chemotherapy resistance is still lacking.

In existing studies, miR-874 is downregulated in all cancers studied and is related to the clinicopathological characteristics of cancer. Therefore, miR-874 is promising as a potential biomarker for the early prediction of cancer. In addition, in recent years, more and more non-cancer diseases have also recognized the evidence related to miR-874, but the specific regulatory mechanism of miR-874 in non-cancer diseases remains to be revealed. Future work is necessary to explore the mechanism of miR-874-related ceRNA network in cancer and non-cancer disease.

Author Contributions

SD, WG and QZ contributed to the conception, design and final approval of the submitted version. QZ, QY and CZ collected and analyzed literature. QZ, CZ, L-hZ, WG, and SD contributed to manuscript writing. All the authors conceived and gave the approval of the final manuscript.

Funding

The research was supported by the grant of Zhejiang Provincial Health Department Project (No. 2020KY680).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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