Target intelligence / Profile preview

microRNA 661 (miR-661)

Target
miR-661
Molecular classification
microRNA, non-coding RNA, epigenetic regulator
01

Overview

microRNA 661 (miR-661) is a human microRNA involved in the post-transcriptional regulation of numerous genes central to metabolic homeostasis, epithelial-mesenchymal transition (EMT), oxidative stress, and cell survival. Its function is highly context-dependent and varies according to cellular type, oncogene/tumor suppressor landscape, and disease state. In colon and breast cancers, miR-661 modulates redox and metabolic pathways, influencing metabolic stress response and EMT—a key step in cancer invasion and metastasis. miR-661 can both suppress and promote tumorigenesis depending on factors such as p53 status: it suppresses tumor aggressiveness in wild-type p53 backgrounds but exacerbates cancer progression in mutant p53 settings by targeting inhibitors like mdm2 and mdm4. Additionally, in pulmonary arterial hypertension, miR-661 acts as an inhibitor of abnormal cell growth through the TRIM29/AKT/mTOR pathway. Due to its diverse biological influence, miR-661 is under investigation as a therapeutic and prognostic biomarker in several cancers and cardiovascular conditions, although direct drug targeting is not currently established[1][2][3][4][5][6][7].

Other names
hsa-miR-661MIR661MIRN661
02

Mechanism of action

As a therapeutic target, modulation (inhibition or overexpression) of miR-661 would alter the expression of its gene targets such as MTA1, INPP5J, hTER, TRIM29, mdm2, mdm4 to regulate cell proliferation, migration, EMT, and survival[1][2][3][7].

03

Biological functions

Regulation of gene expressionInduction of epithelial-to-mesenchymal transition (EMT)Modulation of oxidative stress responseMetabolic reprogramming (glycolysis, pentose phosphate pathway)Cell survival and stress responseSuppression or promotion of cell motility, invasiveness, and anchorage-independent growth dependent on cellular context
04

Disease associations

Cancer (including colon, breast, ovarian, lung, and others)Prognostic marker in cancer (dual roles depending on p53 status in colorectal and breast cancer)Pulmonary arterial hypertension (negative regulator, reduces cell proliferation and migration in hypoxia)
05

Safety considerations

Therapeutic modulation of miR-661 may yield contrasting effects depending on tumor type, genetic context (p53 status), and disease stage[1][3].Broad targeting may cause off-target effects due to miRNA promiscuity and network complexity[1].
06

Interacting drugs

none currently validated; research ongoing for use as a therapeutic and/or prognostic target—miRNAs typically not directly targeted by small molecules, but can be modulated by oligonucleotide therapeutics or delivery vectors. No specific drugs targeting miR-661 are FDA-approved as of 2024.
07

Biomarkers

miR-661 expression level (high or low) in tumor tissue as a prognostic marker in colon and breast cancermiR-661 expression in blood or tissue for monitoring pulmonary arterial hypertension (PAH) progression

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