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DSCAM antisense RNA 1 (DSCAM-AS1)

Target
DSCAM-AS1
Molecular classification
Long non-coding RNA (lncRNA), Other
01

Overview

DSCAM antisense RNA 1 (DSCAM-AS1) is a long non-coding RNA highly upregulated in several cancers, including breast, lung, colorectal, hepatocellular, melanoma, cervical, and gastric cancers. It promotes tumor progression by acting as a competing endogenous RNA (ceRNA), binding and sequestering tumor-suppressor microRNAs, which results in increased oncogene expression. It also interacts with RNA-binding proteins like hnRNPL, contributing to alternative splicing regulation and transcriptome diversity in cancer cells. High expression of DSCAM-AS1 is associated with poorer prognosis, increased proliferation, invasion, metastasis, and drug resistance (notably to tamoxifen in breast cancer). DSCAM-AS1 is being investigated as a diagnostic and prognostic cancer biomarker as well as a potential therapeutic target, though no direct drugs targeting DSCAM-AS1 are presently approved[1][2][4][6].

Other names
M41DSCAM antisense RNA 1 (non-protein coding)
02

Mechanism of action

Acts as a molecular sponge for multiple tumor suppressor microRNAs (e.g., miR-204-5p, miR-384, miR-137, miR-877-5p)[1][2][4]. Promotes oncogene expression by releasing their mRNA from microRNA repression. Interacts with RNA-binding proteins to alter alternative splicing (e.g., hnRNPL)[1][6]. Enhances drug resistance (e.g., tamoxifen) in breast cancer cells via miRNA sponging and upregulation of proliferative pathways[6].

03

Biological functions

Regulation of cell proliferationRegulation of cell cycle (especially G1/S phase transition)Regulation of alternative splicingApoptosis inhibitionRegulation of DNA replicationceRNA ("competing endogenous RNA") regulation of microRNAsAlternative polyadenylation and exon skippingRegulation of tumor suppressor gene expressionOther
04

Disease associations

Cancer (e.g. breast, lung, colorectal, hepatocellular, cervical, melanoma, osteosarcoma, gastric)Tumor progressionDrug resistance (e.g. tamoxifen in breast cancer)
05

Safety considerations

Not directly applicable as a drug target due to its role as an RNA molecule and lack of existing therapeutics; however, targeting could alter splicing or gene regulation with potential off-target effects.Therapeutic targeting may affect multiple downstream pathways given its broad regulatory role[1].
06

Interacting drugs

None established; however, resistance to tamoxifen occurs via upregulation of DSCAM-AS1 in breast cancer[1][6].
07

Biomarkers

DSCAM-AS1 expression is a proposed biomarker for cancer diagnosis, prognosis, and possibly for patient stratification, especially in breast, lung, and colorectal cancer[1][2].

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