Target intelligence / Profile preview

MicroRNA 622 (miR-622)

Target
miR-622
Molecular classification
microRNA, Non-coding RNA, Regulatory RNA
01

Overview

MicroRNA 622 (miR-622) is a small, non-coding RNA molecule (19–24 nucleotides) that post-transcriptionally regulates gene expression by binding to complementary sequences within the 3' untranslated regions of target mRNAs, leading to mRNA degradation or translational repression. It acts as a tumor suppressor in multiple cancer types, including breast, lung, gastric, liver, colorectal, glioma, and renal cancers, primarily by targeting oncogenic pathways such as K-Ras, NUAK1, RNF8, YAP, and others. miR-622 modulates critical cell functions including proliferation, migration, epithelial-mesenchymal transition, apoptosis, and DNA damage repair. Its expression is frequently downregulated in malignancies, and lower levels are associated with more aggressive disease and poorer prognosis. Therapeutic modulation of miR-622, either through mimics or antagomirs, alters cancer cell behavior and holds potential as a biomarker for diagnosis and prognosis, though safety challenges remain due to complex gene regulatory networks and tissue specificity.

Other names
hsa-miR-622MIRN622MIR622hsa-mir-622
02

Mechanism of action

Upregulation of miR-622 can inhibit cancer cell proliferation, invasion, migration, and EMT by repressing target oncogenes such as K-Ras, NUAK1, RNF8, YAP, HIF-1α, CCL18, DYRK2 Downregulation or inhibition can enhance cancer cell survival, proliferation, and migration

03

Biological functions

Post-transcriptional gene regulationRegulation of cell proliferationRegulation of cell migrationRegulation of epithelial-mesenchymal transition (EMT)ApoptosisDNA damage repairUbiquitin-protein ligase regulationSignal transduction via K-Ras, NUAK1, etc.
04

Disease associations

Cancer (breast, gastric, lung, liver, colorectal, renal, glioma)Metastasis and invasionChemoresistance (e.g., platinum resistance in ovarian cancer)Tumor suppression (various contexts)
05

Safety considerations

Therapeutic modulation is challenging due to the pleiotropic and context-dependent effects of miR-622 across different tissues and cancer typesRisk of off-target effects in regulating many genes via seed sequence complementarityPotential induction of chemoresistance (e.g., platinum chemotherapy resistance via overexpression in ovarian cancer)
06

Interacting drugs

Resveratrol (shown to increase miR-622, resulting in anticancer effects)
07

Biomarkers

miR-622 plasma and tissue expression levels for breast cancer and other solid tumorsNUAK1 expression, inversely correlated with miR-622, for breast cancer prognosis

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