Target intelligence / Profile preview

MAMDC2 antisense RNA 1 (MAMDC2-AS1)

Target
MAMDC2-AS1
Molecular classification
Long non-coding RNA (lncRNA), Antisense RNA, Other
01

Overview

MAMDC2 antisense RNA 1 (MAMDC2-AS1), also known as SMC5-DT, is a long non-coding RNA (lncRNA) transcribed from the antisense strand at the MAMDC2 locus on chromosome 9q21.12[1][3][4][5][6]. It does not encode a protein and is not part of canonical receptor, enzyme, or transporter families. Recent research indicates that MAMDC2-AS1 is upregulated in multiple human cell types upon herpes simplex virus 1 (HSV-1) infection and plays a critical regulatory role in the viral life cycle by interacting with Hsp90α, facilitating the nuclear import of viral components and controlling the expression of immediate early viral genes[2][8]. MAMDC2-AS1 knockdown reduces HSV-1 infection and is associated with altered expression of some antiviral factors, though it does not affect its sense gene (MAMDC2) directly[2]. In addition, MAMDC2-AS1 has been linked (mainly through association studies or expression profiling) to colorectal cancer and possibly other diseases, but mechanistic roles in cancer or as a therapeutic target remain unproven[4]. No drugs are known to interact specifically with MAMDC2-AS1, and there are currently no established safety or biomarker roles in clinical practice.

Other names
SMC5-DTSMC5 divergent transcriptMAMDC2-AS1
02

Mechanism of action

Not applicable; MAMDC2-AS1 is not a conventional drug target or protein; functions through RNA-protein interactions (notably with Hsp90α) rather than as a biochemical receptor/enzyme

03

Biological functions

Modulation of host response to viral infectionRegulator of antiviral gene expression upon herpes simplex virus 1 (HSV-1) infectionRNA-protein interaction (notably with Hsp90α)Other
04

Disease associations

Cancer (e.g., colorectal cancer, potential roles in other tumor types)Infection (notably herpes simplex virus 1)Other
05

Biomarkers

No established use as a clinical biomarker, but MAMDC2-AS1 is upregulated during HSV-1 infection and cancers, suggesting possible research utility in these contexts

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