Target intelligence / Profile preview

Muskelin 1 antisense RNA (MKLN1-AS)

Target
MKLN1-AS
Molecular classification
Long non-coding RNA, Non-coding RNA, Antisense RNA, Other
01

Overview

Muskelin 1 antisense RNA (MKLN1-AS) is a cytoplasmic long non-coding RNA located on human chromosome 7q32.3, transcribed from the antisense strand of the MKLN1 gene[3]. MKLN1-AS is highly upregulated in hepatocellular carcinoma tissues and cell lines, with elevated levels associated with vascular invasion, poor overall survival, and reduced recurrence-free survival in patients[1][2][4]. It acts as an oncogenic regulator by promoting cell proliferation, migration, invasion, and angiogenesis through interactions with specific microRNAs (notably miR-654-3p and miR-22-3p)[1][2][4]. MKLN1-AS operates through the molecular sponge (ceRNA) mechanism, modulating the levels of oncogenic proteins such as ETS1, HDGF, and YAP1 via sequestration of miRNAs. Knockdown of MKLN1-AS suppresses tumor growth and enhances sensitivity to the multi-kinase inhibitor lenvatinib, indicating its potential as a therapeutic and prognostic target in HCC[1][4]. There is currently no evidence that MKLN1-AS serves as a classical drug target outside of cancer biology, and its therapeutic application remains investigational.

Other names
MKLN1-ASMKLN1-AS2MKLN1 antisense RNA 2MKLN1 ASmuskelin 1 antisense RNA
02

Mechanism of action

Knockdown of MKLN1-AS enhances efficacy of lenvatinib and increases apoptosis. Acts as a competitive endogenous RNA (ceRNA) by sponging microRNAs and derepressing downstream oncogenes (ETS1, HDGF, YAP1).

03

Biological functions

Cell proliferationCell migrationCell invasionAngiogenesisApoptosis regulationPrognostic biomarkerMolecular sponge for microRNAs (miR-654-3p, miR-22-3p)
04

Disease associations

Cancer (specifically hepatocellular carcinoma)MetastasisPoor prognosis in cancerDrug resistance (implicating response to lenvatinib)
05

Safety considerations

Therapeutic targeting of lncRNAs is experimental—potential off-target effects and unclear delivery strategiesRole limited to HCC; little evidence for safety or risk outside experimental cancer therapeutics
06

Interacting drugs

Lenvatinib
07

Biomarkers

MKLN1-AS expression levels (prognostic for overall and disease-free survival in HCC)High MKLN1-AS correlates with vascular invasion and aggressive tumor phenotype

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