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BRAF-activated non-protein coding RNA (BANCR)

Target
BANCR
Molecular classification
Long non-coding RNA (lncRNA), Other
01

Overview

BRAF-activated non-protein coding RNA (BANCR, also known as LINC00586) is a long non-coding RNA initially identified as induced by BRAF^V600E^ mutation, particularly in melanoma[5]. It is 693 nucleotides in length and located on chromosome 9[1]. BANCR is overexpressed in multiple cancers, including colorectal, melanoma, and cervical carcinomas. Mechanistically, BANCR functions primarily as an oncogenic lncRNA, promoting tumor cell proliferation, migration, invasion, epithelial-to-mesenchymal transition (EMT), and generally facilitating tumor progression. In colorectal cancer, BANCR recruits the histone demethylase LSD1 to the ASXL1 gene promoter, leading to epigenetic silencing of the tumor suppressor ASXL1 through H3K4me2 demethylation, thereby promoting oncogenic processes. In cervical cancer, BANCR modulates proliferation and apoptosis in part by regulating the expression of CREB1, via antagonism of miR-582-5p[1][4]. High BANCR expression is associated with poor prognosis and aggressive disease, and its knockdown suppresses tumorigenic properties in experimental models[1][2][4][5][3]. It is under investigation as a potential biomarker and therapeutic target, but no approved or clinically established BANCR-targeting drugs exist at this time.

Other names
LINC00586BANCRBRAF-activated lncRNA
02

Mechanism of action

Regulation of gene expression via epigenetic silencing; recruits LSD1 to the ASXL1 promoter, leading to H3K4me2 demethylation and transcriptional repression of ASXL1; may regulate CREB1 via miR-582-5p in some cancers[1][4].

03

Biological functions

Cell proliferationCell migrationApoptosisEpithelial-to-mesenchymal transition (EMT)Transcriptional regulationEpigenetic regulationTumorigenesis
04

Disease associations

Cancer, specifically colorectal cancer (CRC) and melanoma, with roles suggested in cervical cancer
05

Safety considerations

Targeting lncRNAs for therapy is challenged by delivery specificity, off-target effects, and incomplete understanding of broad regulatory networks; further research needed for safe, effective therapy development[1].
06

Interacting drugs

None currently established
07

Biomarkers

High expression in tumor tissues, especially CRC and melanoma, is associated with poor prognosis, cell proliferation, invasion, EMT, and tumorigenicity[1][2].

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