Target intelligence / Profile preview

Musculoaponeurotic fibrosarcoma oncogene homolog (c-Maf)

Target
c-Maf
Molecular classification
Transcription factor, bZIP (basic leucine zipper) transcription factor, AP-1 superfamily member
01

Overview

Musculoaponeurotic fibrosarcoma oncogene homolog (c-Maf) is a basic leucine zipper (bZIP) transcription factor encoded by the MAF gene on chromosome 16. It is a member of the AP-1 superfamily and the Maf family, with major roles in regulating cell differentiation and developmental processes across a variety of tissues, including lens cells, neural tissue, kidney, bone, erythrocyte formation, and pancreatic islets. c-Maf is also a critical immune regulator in lymphocytes, programming macrophages and controlling tolerance. As an oncogene and transcriptional programmer, c-Maf is implicated in cancer biology (including musculoaponeurotic fibrosarcoma and tumor-associated macrophages). It interacts with other transcriptional co-regulators such as CREBBP, EP300, MYB, and SOX9 to regulate its target genes. Disruption of c-Maf function results in severe developmental and immunological defects, making it a potential target for therapeutic intervention in cancer and immune-related diseases, but also presenting significant safety concerns due to its broad biological functions.

Other names
Mafproto-oncogene c-MafV-maf musculoaponeurotic fibrosarcoma oncogene homolog
02

Mechanism of action

Transcriptional modulation: drugs or agents that would inhibit or modulate c-Maf function act by altering its DNA binding and transcriptional regulation activity

03

Biological functions

Cell differentiationDevelopmental processesLens fiber cell differentiationMechanoreceptor regulationRenal tubular cell developmentChondrocyte differentiationFetal erythropoiesisPancreatic hormone production (glucagon)Immune tolerance in lymphocytesGene transcription regulationMacrophage programming in cancer
04

Disease associations

Cancer (oncogene associated with musculoaponeurotic fibrosarcoma)Lens development disordersKidney development disordersPancreatic endocrine dysfunctionImmunological tolerance/immune disordersLung cancer macrophage reprogramming
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Safety considerations

Potential embryonic or perinatal lethality if gene function is disrupted across all tissuesSystemic developmental impact due to broad regulatory roleImmunological dysregulation (Treg-TH17 balance, tolerance disruption)
06

Biomarkers

c-Maf expression levels in immune cells (for tolerance and autoimmune monitoring)c-Maf expression in cancer tissues (for tumor subtype/oncogenicity assessment)

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