Target intelligence / Profile preview

Family with sequence similarity 117 member B (FAM117B)

Target
FAM117B
Molecular classification
Other (protein of unknown superfamily; not a receptor, enzyme, transporter, or classic signal transducer), Cytoplasmic protein with functional protein-protein interaction motifs[1][3][4]
01

Overview

Family with sequence similarity 117 member B (FAM117B) is a cytoplasmic protein characterized by an ETGE protein-protein interaction motif, enabling it to bind Kelch-like ECH-associated protein 1 (KEAP1) and compete with nuclear factor erythroid 2–related factor 2 (NRF2) for KEAP1 binding[1][3]. This competition reduces ubiquitination and proteasomal degradation of NRF2, resulting in increased NRF2 signaling—a pathway central to oxidative stress response, tumor development, and chemoresistance. FAM117B promotes gastric cancer cell growth and resistance to chemotherapy, is overexpressed in gastric tumors, and may have additional clinical significance based on genetic association with neurodegenerative (juvenile ALS), vascular, and immune-mediated diseases[1][2][3][4]. While currently not a target of any approved drugs, its role in malignancy and other disease contexts positions it as a candidate therapeutic target and biomarker for further research.

Other names
ALS2CR13Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 13FLJ38771Protein FAM117BAmyotrophic lateral sclerosis 2 (juvenile) chromosome region candidate 13
02

Mechanism of action

Not applicable; no drugs are known to target this protein directly[1][3][4]

03

Biological functions

Regulation of KEAP1/NRF2 antioxidant signalingModulation of protein ubiquitinationPromotion of cell proliferation and drug resistance in cancer[1][3]Suggested involvement in vascular integrity and immune response based on genetic association studies[2]
04

Disease associations

Cancer (notably gastric cancer initiation, progression, chemoresistance)[1][3][5]Neurodegenerative disease (genetic locus association with juvenile amyotrophic lateral sclerosis)[4]Cardiovascular disease (association with cerebral small vessel disease and lacunar stroke)[2]Inflammation (susceptibility locus identified in sarcoidosis GWAS)[2]Other (suggested role in vascular and immune-mediated pathology from genetic studies)[2]
05

Biomarkers

Overexpression of FAM117B (with NRF2 co-overexpression) as a potential prognostic biomarker in gastric cancer patients[1][3]Genomic alterations (risk alleles) associated with susceptibility in intracerebral hemorrhage, lacunar stroke, and sarcoidosis[2]

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