Target intelligence / Profile preview

microRNA 636 (miR-636)

Target
miR-636
Molecular classification
MicroRNA (miRNA), Non-coding RNA
01

Overview

microRNA 636 is a human non-coding small RNA molecule located on chromosome 17q25.1[1]. As a member of the microRNA family, it regulates gene expression by binding to target mRNAs, primarily resulting in transcriptional inhibition or mRNA degradation. miR-636 acts as a tumor suppressor in ovarian and cervical cancers by reducing the expression of target genes such as Gli2, a key transcription factor in the Hedgehog signaling pathway. Its overexpression inhibits cell proliferation, migration, and epithelial-mesenchymal transition (EMT), and induces cell cycle arrest. Reduced expression of miR-636 is found in several cancers, and it functions as a diagnostic biomarker for some malignancies and hematological conditions. The molecule also shows differential expression patterns linked to glucocorticoid resistance and myelodysplastic syndrome, highlighting its importance in therapeutic research[1][2][3].

Other names
miR-636MIR636hsa-mir-636MIRN636
02

Mechanism of action

Acts via post-transcriptional silencing of target mRNAs by binding to 3'-UTR regions, inhibiting translation or promoting mRNA degradation. Specifically inhibits expression of *Gli2* (a transcription factor in the Hedgehog signaling pathway), thereby blocking cell proliferation, migration, EMT, and promoting cell cycle arrest. May influence glucocorticoid receptor alpha (GR-α) levels, affecting glucocorticoid sensitivity.

03

Biological functions

Regulation of gene expression (post-transcriptional)Suppression of cell proliferationInhibition of cell migrationInduction of cell cycle arrest in G0/G1 phaseModulation of epithelial-mesenchymal transition (EMT)
04

Disease associations

Cancer (notably ovarian, cervical, and prostate cancers)Myelodysplastic syndromes (MDS)Glucocorticoid resistance in hematological malignanciesPossibly urothelial carcinomaOther (potential biomarker for several cancers)
05

Safety considerations

Major safety concerns not described; as with miRNA-based therapy, off-target effects and systemic delivery risk may apply.Therapeutic challenges include specific, effective delivery to target tissues and avoiding unintended silencing of non-target genes.
06

Interacting drugs

No specific drugs directly targeting miR-636 are currently listed in the literature

1 more in the full profile.

07

Biomarkers

Downregulated levels serve as biomarkers for early diagnosis of prostate cancer and urothelial carcinomaDiagnostic marker for myelodysplastic syndromes

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