Target intelligence / Profile preview

MicroRNA 663a (miR-663a)

Target
miR-663a
Molecular classification
MicroRNA (miRNA), Non-coding RNA, Small regulatory RNA
01

Overview

MicroRNA 663a (miR-663a) is a small, non-coding RNA molecule that post-transcriptionally regulates gene expression by targeting mRNAs for degradation or translational repression. It has a key role in controlling cell proliferation, cell cycle progression, and cellular migration/invasion, partly through the regulation of target genes such as JunD and TTC22V1[2][3]. Downregulation of miR-663a is associated with increased cancer progression and metastasis in several cancers, including colon and non-small cell lung cancer, where it typically acts as a tumor suppressor[2][3]. Higher levels have also been associated with cancer progression in certain prostate cancer contexts[4], underscoring its complex, tissue-specific functions. Its expression profiles can serve as biomarkers for cancer diagnosis or prognosis. While not currently the target of any approved drugs, miR-663a is a focus of research using oligonucleotide-based mimics or inhibitors that may modulate its therapeutic potential.

Other names
hsa-miR-663aMIR663AmiR-663aMIR663MIRN663hsa-mir-663hsa-mir-663amir-663amicroRNA 663microRNA-663a
02

Mechanism of action

Post-transcriptional gene silencing: miR-663a binds to the 3′ untranslated region (UTR) of specific target mRNAs (e.g., JunD, TTC22V1), resulting in their degradation or translational repression. miRNA sponging: Competing endogenous RNAs (e.g., lncRNA MALAT1) can sequester miR-663a, modulating its regulatory effects.

03

Biological functions

Regulates cell proliferation (by modulating cell cycle-related genes)Regulates cell cycle progression (notably G1-S transition)Modulates cell invasion and migration (through targets such as JunD and TTC22V1)Influences apoptosis (apoptotic processes are among regulated pathways)Regulates DNA repair, cell junction assembly, and response to oxidative stress
04

Disease associations

Cancer (downregulation in colon cancer, non-small cell lung cancer; involved in prostate cancer and potentially others)Inflammation (linked to inflammation-associated gene expression)Possibly other tissue/organ-specific roles (as effects may be tissue-dependent)
05

Safety considerations

Off-target effects are an issue in the development of miRNA-directed therapeutics, including potential effects on non-intended gene networksTissue specificity: Effects of miR-663a can be tissue- or context-dependent and may act as a tumor suppressor or promoter in different settings, complicating therapeutic strategyDelivery and stability challenges for miRNA-based therapeutics (common to all miRNA targets)
06

Interacting drugs

No small molecule therapeutic drugs are known to directly target miR-663a as of 2024 search data. However, experimental miRNA mimics and inhibitors (antisense oligonucleotides) are used to modulate its activity in research settings
07

Biomarkers

Expression levels of miR-663a in tumor tissues (e.g., colon cancer, lung cancer) may serve as diagnostic/prognostic biomarkers for cancer progression and metastasisTTC22V1 expression: Inversely correlated with miR-663a, may signal metastatic risk in colon cancer

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