Target intelligence / Profile preview

Transmembrane protein 120B (TMEM120B)

Target
TMEM120B
Molecular classification
Transmembrane protein, Nuclear envelope transmembrane protein, Other
01

Overview

Transmembrane protein 120B (TMEM120B) is a multi-pass transmembrane protein, localized primarily to the nuclear envelope and endoplasmic reticulum, composed of six transmembrane domains and a coiled-coil domain at the N-terminus[2][3][5]. It is implicated in adipocyte differentiation and metabolism, where it modulates the expression of key adipogenic genes and may contribute to tissue-specific lipid metabolism[2][5]. In cancer, TMEM120B is upregulated in multiple solid tumors, where it promotes tumor cell proliferation, invasion, maintenance of cancer stemness, and resistance to chemotherapeutic agents like doxorubicin and docetaxel by activating β1-integrin–FAK–TAZ–mTOR signaling pathways and stabilizing the cytoskeletal regulator MYH9 (myosin heavy chain 9)[3]. TMEM120B does not display ion channel activity[2]. Its expression in cancer patients is associated with advanced disease stage and poor prognosis, underscoring its potential as a prognostic biomarker and modulator of chemoresistance, though it is not a currently established direct therapeutic target[3][2][5].

Other names
TMEM120BTransmembrane 120B
02

Mechanism of action

TMEM120B overexpression increases resistance to chemotherapeutics (such as doxorubicin and docetaxel) by activating the β1-integrin–FAK–TAZ–mTOR signaling axis[3]. Not a direct drug target, but modulates response to chemotherapy through cellular signaling changes[3]

03

Biological functions

Adipogenesis (fat cell differentiation)[2][5]Regulation of gene expression involved in adipocyte biology[5]Modulation of cell proliferation and invasion (in cancer)[3]Maintenance of stemness in cancer stem cells[3]Regulation of focal adhesion assembly and mechanical signaling[3]Protein stabilization (stabilizes MYH9, myosin heavy chain 9)[3]
04

Disease associations

Cancer (notably breast and other solid tumors: increased expression associated with tumor progression, metastasis, stemness, and chemoresistance)[3]Obesity/metabolic disease (role in adipocyte differentiation and nuclear envelope biology)[5]Other
05

Safety considerations

No specific drug-related safety concerns documented for targeting TMEM120B; limited information currently available.As a potential modulator of stemness and chemoresistance, inhibition may impact normal adipogenesis or essential cell processes[3][5]
06

Interacting drugs

Doxorubicin (chemoresistance interaction reported)[3]

1 more in the full profile.

07

Biomarkers

TMEM120B expression is a potential biomarker for poor prognosis and chemoresistance in breast cancer and other solid tumors[3]Elevated TMEM120B correlates with advanced TNM stage, lymph node metastasis, and poor patient outcomes in cancer[3]

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