Target intelligence / Profile preview

Transmembrane protein 161A (TMEM161A)

Target
TMEM161A
Molecular classification
Other (Transmembrane protein), Not a G protein-coupled receptor, ion channel, enzyme, transporter, or receptor by conventional pharmacological criteria, Member of the TMEM161 protein family
01

Overview

Transmembrane protein 161A (TMEM161A) is a membrane-associated protein belonging to the TMEM161 family, implicated in the adaptive response to oxidative stress. It influences cellular stress tolerance and DNA damage pathways, notably providing protection against oxidant-induced apoptosis. TMEM161A is expressed in various tissues and particularly implicated in *bone formation*, acting as a suppressor of osteogenic differentiation via regulation of the P38 MAPK pathway. Overexpression reduces osteoblast differentiation and bone mineral deposition, while knockout increases bone strength and thickness in mice. TMEM161A has also been observed as a tumor-associated antigen in non-small cell lung cancer, suggesting some disease relevance, but is not an established therapeutic target.

Other names
TMEM161ATransmembrane protein 161AUNQ582/PRO1152AROS-29FLJ39645FLJ20422Adaptive response to oxidative stress protein 29AROS29
02

Mechanism of action

Not applicable; no drugs are known to act directly on TMEM161A. Experimental inhibition with P38 MAPK pathway inhibitors (e.g., SB203580) was used mechanistically in cell studies, but not clinically or as a TMEM161A-directed intervention.

03

Biological functions

Cellular response to ultraviolet (UV) stressRegulation of cellular response to general stress, including *oxidative stress* protectionResponse to retinoic acidSuppression of oxidant-induced DNA damage and apoptosisNegative regulation of osteoblast differentiation and bone formation via modulation of the P38 MAPK signaling cascade
04

Disease associations

*Cancer*: Overexpressed in some human non-small cell lung cancers and considered a tumor-associated antigen*Bone disease*: Influences bone density and strength, with knockouts showing increased bone thickness and mineral density in murine models*Other*: Modulation of stress responses may be relevant for other pathological processes, but direct roles in inflammation, neurodegeneration, cardiovascular disease, or infection are not substantiated in current literature
05

Biomarkers

*Alkaline phosphatase (ALP)* and *Osterix (Osx)* are used experimentally to monitor downstream functional effects of TMEM161A on osteogenesis, but TMEM161A itself is not established as a biomarker for patient selection or drug efficacy

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