Table 1.
miR | Mechanism of action | Cell Type Described |
Inside EVs | Hippo Signaling | Ref. |
---|---|---|---|---|---|
miR-10a/b | Activates pro-metastatic genes, promoting tumor cell invasion and metastasis. Migration. | Ovarian cancer, bladder cancer, breast cancer, esophageal cancer, and gastric cancer cells. ECs. | + | [164,165,166,167,168,169,170,171] | |
miR-17-5p*/3p | Survival, proliferation, migration, regeneration. EC morphogenesis and angiogenesis. Target TIMP1 Tsp1, PTEN. |
ECs, tumor cells | + | ([78,88,89,172] | |
miR-19a/b-1*/-2⁎⁎ | Help to suppress the sensitivity to anticancer drugs, and anti-apoptotic. EC morphogenesis and tumor angiogenesis. Regeneration Target TIMP1 Tsp1, PTEN. |
Gastric cancer cell line, ECs, leukemia cells (K562). | + | [78,88,89,140,143,172,173] | |
miR-20a*/b-5p/3p⁎⁎ | EC morphogenesis and tumor angiogenesis. Regeneration Target TIMP1 Tsp1, PTEN. |
Breast cancer, myeloma cells, ECs. | ? | ([139,140] |
|
miR-21 | Proliferation, EMT, angiogenesis. Repair spinal cord microvasculature. Maintaining of vSMC phenotype. | In vitro in vivo models (several tumors, vascular repair, healthy). | + | [83,86,97,134] | |
miR-23a/b-3p | Proliferation, tumor progression, metastasis. | Prostate cancer. | [90] | ||
miR-25-3p*** | Up-regulation of miR-25 was correlated migration and invasion. | Esophageal squamous cell carcinoma. |
[174] |
||
miR-26a-1-5p/3p | c-Myc increases miR-26a expression. miR-26a activates Akt signaling through direct PTEN targeting and increases VEGF, MMP2 expression. Increases proliferation and invasiveness. | High-grade glioma, glioblastoma multiforme, lung cancer cells | + | [90,91,175,176] |
|
miR-26b | Enhance growth, survival, and tube formation through PTEN targeting. Inhibit the proliferation, migration, and EMT in epithelial cells through prostanoid pathway inhibition. |
EC, epithelial cells | [177,178,179] |
||
miR-29a-5p | Pro-angiogenic YAP induces miR-29 to inhibit PTEN translation which activates PI3K–mTOR signaling to regulate proliferation and cell size. |
Lung cancer cells, ECs, epithelial cells, mice. |
+ |
([138],[180] | |
miR-92a-1-5p*/a-2⁎⁎ miR-92b-3p |
EC morphogenesis and tumor angiogenesis. Regeneration Target TIMP1 Tsp1, PTEN. |
ECs, leukemia cells (K562). |
+ |
[78,89,90,181,182,183] | |
miR-93-5p⁎⁎⁎ | High proliferation, anti-apoptotic, and influence tumor size. Cisplatin resistance, suppressing PTEN and over activating AKT pathway. Angiogenesis | Osteosarcoma cells, ovarian cancer, ECs, mouse hearts | + |
([135,184,185] |
|
miR-103a-3p | Downregulation of angiogenesis inhibitors expression, like TIMP3. Promotes cell transformation, and disrupt the endothelium integrity, increasing the vascular permeability. | Endometrial and hepatocarcinoma cells, ECs. | + | [127,128,129,130,131,186] | |
miR-105-5p | Vascular permeability disruption. Downregulates ZO-1 expression, altering the vascular junctions. | In vitro, ex vivo and in vivo assay in rodents. | [133] | ||
miR-106a-5p/3p⁎⁎/ miR-106b-5p/3p⁎⁎⁎ | |||||
miR-130a/b | Proliferation, migration, and anti-apoptotic | Glioma cell lines, squamous cell carcinoma. | [187,188] | ||
miR-181b/c-5p | |||||
miR-193/a-3p | Cell proliferation, migration, 5-FU chemoresistance, and in vivo tumorigenicity through PTEN targeting. Contradictory, functions like tumor suppressor miRNA, inhibiting migration, invasion, and EMT in vitro and metastasis in vivo in lung cancer. |
Gastric cancer cell lines |
([189,190] |
||
miR-200c-5p/3p | Alters wound-healing capacity and colony formation. MT1-MMP (Membrane type-1 matrix metalloproteinase) and PTEN expression are regulated. | Pancreatic cancer cell. | |||
miR-205-5p | Directly targets SMAD4, CYR61, CTFG, PTEN. Promotes proliferation, anti-apoptotic, migration, chemoresistance, and tumorigenesis in vivo. Regulated Erb/HER, PTEN/AKT axis. Biomarker for cervical cancer patients. |
Ovarian cancers (OC) with poor diagnostic, cervical cancer cells, breast, lung, and NSCLC cancers. |
[93,94,95,191,192,193,194] |
||
miR-221-3p | Downregulates PTEN and activates PI3K/Akt signaling. Induce cell survival, proliferation, carmustine, and cisplatin resistance. | Osteosarcoma cells, Epithelial ovarian cancer (EOC) cells | [195],[196] | ||
miR-223 | Downregulates PTEN and activates PI3K/Akt signaling. | Ovarian cancer cells | [124] | ||
miR-301a/b | M2 macrophage polarization through PTEN targeting. Promote migration, invasion, EMT, and facilitate the lung metastasis of pericytes. | Pancreatic cancer cells | + | [126] | |
miR-382-5p | Target PTEN and consequent activation of AKT/mTOR signaling. Increases proliferation, migration, and apoptosis avoidance. Increases vascular EC proliferation, migration, and tube formation. | Hemangioma-derived endothelial cell, hypoxia in human gastric cancer cells | [92,197] |
||
miR-425 | MALAT1 interacts with miR-425 preventing PTEN silencing. Induce apoptosis | Plasma and plasma exosomes |
[141] |
||
miR-494-5p/3p | Target PTEN and subsequent activation of AKT/eNOS pathway. Enhances proliferation, migration, invasion, and promotes angiogenesis. | Hypoxic lung cancer cells, glioblastoma cells, ECs. | [198,199] | ||
miR-638 | Dual PTEN and p53-targeting. Cell migration, invasion, proliferation, and anchorage-independent growth. | Exogenous expression model in prostate cancer cells | [163] | ||
miR-939 | ? | ([132] |
miR-17/92 cluster: located in chromosome 13, encodes miR-17, miR-18a, miR-19a, miR-20a, miR-19b-1 and miR-92a-1, lso known as oncomiR-1.
miR-106a/363 cluster: located on chromosome X, encodes miR-106a, miR-18b, miR-19b-2, miR-20b, miR-92a-2, and miR-363.
miR-106b/25 cluster: located in chromosome 7, encodes miR-106b, miR-93, and miR-25.