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Updated: Apr 15, 2026

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Published on: May 19, 2016
[TRAF4, a multifaceted protein involved in carcinoma progression]
Adrien Rousseau1, Catherine Tomasetto1, Fabien Alpy1
1Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département de Génomique Fonctionnelle et Cancer, 1 rue Laurent Fries, 67404 Illkirch, France - Institut National de la Santé et de la Recherche Médicale (INSERM), U 964, 67404 Illkirch, France - Centre National de la Recherche Scientifique (CNRS), UMR 7104, 67404 Illkirch, France - Université de Strasbourg, 67404 Illkirch, France.
TRAF4 protein, found in tight junctions (TJs), is overexpressed in carcinomas and drives tumor progression. This review explores TRAF4
Area of Science:
- Cell Biology
- Oncology
- Molecular Biology
Context:
- Epithelial cells form cohesive tissues via junctional complexes, crucial for tissue architecture and function.
- Tight junctions (TJs) maintain apicobasal polarity, essential for epithelial integrity.
- Disruption of TJs is implicated in carcinoma formation and progression.
Purpose:
- To review recent findings on the role of TRAF4 in carcinogenesis.
- To present the TRAF proteins family and the molecular mechanisms of TRAF4 localization to TJs.
- To discuss the functions of TRAF4 in cancer development and the significance of lipid binding by TRAF proteins.
Summary:
- TRAF4 is a protein dynamically localized to TJs and frequently overexpressed in carcinomas.
- TRAF4 plays multiple roles in tumor progression, with its localization to TJs involving lipid binding.
- The review covers the TRAF protein family, TRAF4's TJ targeting mechanism, its roles in carcinogenesis, and the functional relevance of TRAF protein lipid-binding capabilities.
Impact:
- Understanding TRAF4's role in carcinogenesis may reveal new therapeutic targets for cancer treatment.
- Elucidating the lipid-binding function of TRAF proteins could offer insights into cellular signaling pathways.
- This review consolidates current knowledge, providing a foundation for future research into TRAF4 and cancer.
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