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VIM antisense RNA 1 (VIM-AS1)

Target
VIM-AS1
Molecular classification
Long non-coding RNA (lncRNA), Natural antisense transcript, Epigenetic regulator (via RNA:DNA R-loop formation)
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Overview

VIM antisense RNA 1 (VIM-AS1) is a 1.8-kilobase long non-coding RNA transcribed antisense to the vimentin gene, enriched in the nucleus and implicated as both an epigenetic modulator and a cancer-related biomarker. Its mechanism involves R-loop formation at the VIM locus, modulating chromatin structure and vimentin gene expression. VIM-AS1 has oncogenic roles in several cancers, where it promotes epithelial-mesenchymal transition, cell proliferation, migration, and metastasis through regulation of signaling pathways like Wnt/β-catenin and NF-κB, and impacts apoptosis in a context-dependent manner. Importantly, the expression level of VIM-AS1 can serve as a prognostic marker for tumor progression and patient outcome in specific cancer types. No approved drugs directly target VIM-AS1, but its biological activities suggest therapeutic potential for future antigene strategies, though context-dependent safety concerns remain.

Other names
VIM-AS1VIM antisense RNA 1BC078172 transcript
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Mechanism of action

N/A (No drugs targeting VIM-AS1 have mechanistic evidence; conceptually, antisense oligonucleotides or RNAi may silence VIM-AS1 and thus affect cancer cell proliferation, migration, and apoptosis)

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Biological functions

Regulation of gene expression (activates/silences vimentin transcription via antisense mechanisms and R-loop formation)Promotion of cell proliferationInduction of metastasis and migrationPromotion of epithelial-mesenchymal transition (EMT)Regulation of apoptosis (context-dependent, can facilitate or suppress apoptosis)Potential modulation of Wnt/β-catenin and NF-κB signaling pathways
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Disease associations

Cancer (implicated in multiple cancers: gastric, prostate, lung adenocarcinoma, oral, breast, and colorectal)May serve as diagnostic and prognostic biomarker in cancer (gastric cancer, lung adenocarcinoma, etc.)
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Safety considerations

Functional specificity and context-dependent effects: VIM-AS1 may promote oncogenesis in some cancers (gastric, prostate), but suppress metastasis or promote cell death in others (lung adenocarcinoma, breast)Limited mechanistic data: Direct targeting could affect vimentin and downstream processes, possibly leading to unintended consequences in cell structural integrity or EMT
06

Biomarkers

VIM-AS1 expression level (used as a biomarker for cancer patient prognosis and diagnosis)Co-expressed genes in VIM-AS1 pathways (e.g., FZD1, β-catenin, cyclin D1, C-myc) may have auxiliary biomarker value

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