Target intelligence / Profile preview

MicroRNA-587 (miR-587)

Target
miR-587
Molecular classification
MicroRNA, Non-coding RNA
01

Overview

MicroRNA-587 is a small, non-coding RNA involved in post-transcriptional regulation of mRNA by binding to complementary sequences, predominantly in the 3'UTRs of target genes. In cancer biology, miR-587 is implicated in cell cycle progression, apoptosis regulation, migration, and invasion, with its roles being highly context-dependent. In colorectal cancer, miR-587 drives resistance to 5-fluorouracil-induced apoptosis by targeting PPP2R1B, leading to increased AKT signaling and decreased cell death. Conversely, in hepatocellular carcinoma, miR-587 functions as a tumor suppressor by targeting ribosomal protein SA (RPSA), inhibiting proliferation and invasion. Expression levels and functional roles of miR-587 are variable across tumor types, suggesting its utility as a biomarker for prognosis and therapy response, though its therapeutic targeting presents significant challenges due to its widespread effects and lack of clinical agents directly modulating this miRNA.

Other names
hsa-miR-587MIR587MIRN587hsa-mir-587
02

Mechanism of action

For 5-fluorouracil: miR-587 confers resistance by downregulating PPP2R1B, leading to AKT activation and reduced apoptosis. For AKT inhibitors (MK-2206): they overcome miR-587-mediated resistance by blocking downstream AKT phosphorylation. For experimental anti-miR oligonucleotides: they inhibit miR-587 to restore PPP2R1B expression and resensitize to chemotherapy.

03

Biological functions

Regulation of gene expression (primarily post-transcriptional silencing by binding to 3'UTRs of target mRNAs)Cell cycle regulation (including SubG1-phase cell cycle arrest)Apoptosis (regulation and antagonism, context-dependent)Cell proliferation (inhibitory or stimulatory depending on cellular context)Migration and invasion regulation (particularly in hepatocellular carcinoma)Chemoresistance (notably to 5-fluorouracil)
04

Disease associations

Cancer (multiple types: colorectal, hepatocellular, breast, prostate, glioblastoma)Chemoresistance (specifically 5-fluorouracil resistance in colorectal cancer)Tumor suppression or promotion depending on cellular/tissue context
05

Safety considerations

Potential for off-target effects and broad impact on multiple gene expression pathways if targeted therapeuticallyTumor context–dependency: miR-587 may act as a tumor suppressor or oncogene depending on cancer type and microenvironmentLack of current clinical therapeutics targeting miR-587; primarily preclinical data
06

Interacting drugs

5-Fluorouracil (5-FU)

2 more in the full profile.

07

Biomarkers

miR-587 expression level in tumor tissue (for 5-fluorouracil resistance in colorectal cancer)miR-587 tissue expression (as a diagnostic/prognostic biomarker in hepatocellular carcinoma)PPP2R1B expression (inversely correlated with miR-587)

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