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SOCS2 antisense RNA 1 (non-protein coding) (SOCS2-AS1)

Target
SOCS2-AS1
Molecular classification
Long non-coding RNA (lncRNA), Other (non-protein coding, antisense RNA)
01

Overview

SOCS2 antisense RNA 1 (SOCS2-AS1) is a long non-coding RNA transcribed from the antisense strand of the SOCS2 gene locus. SOCS2-AS1 acts as a tumor suppressor in endometrial and colorectal cancer, where its reduced expression is associated with advanced disease and poor prognosis[1][4]. It is predominantly cytoplasmic and regulates cancer cell proliferation, cell-cycle progression, apoptosis, and metastasis. SOCS2-AS1 achieves these effects by interacting with key proteins (such as AURKA) and by modulating gene expression through mechanisms such as miRNA sponging (miR-1264), which impacts SOCS2 levels and subsequently influences the JAK/STAT signaling pathway[1][2][4]. In androgen-driven prostate cancer contexts, SOCS2-AS1 modulates chromatin cofactor recruitment in concert with the androgen receptor, shaping the epigenetic landscape of target genes[2]. SOCS2-AS1 itself is regarded as a potential therapeutic target and biomarker for specific drug strategies (notably, AURKA-inhibition) in certain cancers[1].

Other names
SOCS2 antisense RNA 1SOCS2-AS1SOCS2 antisense RNA 1 (non-protein coding)
02

Mechanism of action

Drugs altering AR (androgen receptor) activity or AURKA (Aurora kinase A) protein stability may indirectly affect SOCS2-AS1 function and associated pathways. SOCS2-AS1 enhances degradation of AURKA through the ubiquitin-proteasome pathway. SOCS2-AS1 regulates SOCS2 by sponging miR-1264, thus affecting downstream JAK/STAT-related signaling.

03

Biological functions

Regulation of cell proliferationInduction of cell-cycle arrest and apoptosisModulation of migration and invasionEpigenetic regulation (modulates androgen receptor function and chromatin cofactor recruitment)Regulation of gene expression through miRNA sponging (e.g., miR-1264)
04

Disease associations

Cancer (particularly endometrial cancer and colorectal cancer: tumor suppressor and prognostic marker)Prostate cancer (linked to cell proliferation and migration in androgen-regulated contexts)
05

Safety considerations

The major therapeutic challenge is the lack of directly targeted drugs; modulation would require RNA-based therapeutics (e.g., antisense oligonucleotides, RNA mimics) whose safety is not yet well established in clinical settings.Potential off-target effects due to widespread impact on cell cycle and apoptosis if therapeutically modulated
06

Interacting drugs

No directly approved drugs known to target SOCS2-AS1; however, it may serve as a biomarker for AURKA-inhibitor response in endometrial cancer

1 more in the full profile.

07

Biomarkers

SOCS2-AS1 expression level (prognostic marker for cancer progression and survival in endometrial and colorectal cancer)May serve as a biomarker for selection of AURKA-inhibitor therapy in endometrial cancer

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