TM4SF5-mediated protein-protein networks and tumorigenic roles
1Department of Pharmacy, Research Institute of Pharmaceutical Sciences, Tumor Microenvironment Global Core Research Center, Medicinal Bioconvergence Research Center, College of Pharmacy, Seoul National University, Seoul 151-742, Korea.
Abstract:
Transmembrane 4 L six family member 5 (TM4SF5), as a membrane glycoprotein with 4 transmembrane domains, is similar to the tetraspanins in terms of membrane topology and plays important roles in tumorigenesis and tumor metastasis. Especially, TM4SF5 appears to form a massive protein-protein complex consisting of diverse membrane proteins and/or receptors in addition to cytosolic signaling molecules to regulate their signaling activities during the pathological processes. TM4SF5 is shown to interact with integrins α2, α5, and β1, EGFR, IL6R, CD151, focal adhesion kinase (FAK), and c-Src. This review focuses on the significance of the interactions with regards to TM4SF5-positive tumorigenesis and metastasis.
Insights
Transmembrane 4 L six family member 5 (TM4SF5) protein complexes regulate tumor growth and spread. Understanding TM4SF5 interactions is key to targeting tumorigenesis and metastasis.
Area of Science:
- Molecular biology
- Cell biology
- Cancer research
Background:
- Transmembrane 4 L six family member 5 (TM4SF5) is a membrane glycoprotein implicated in cancer progression.
- TM4SF5 shares structural similarities with tetraspanins and possesses four transmembrane domains.
- It is known to form large protein complexes involved in cellular signaling.
Purpose of the Study:
- To review the significance of TM4SF5 interactions in tumorigenesis and metastasis.
- To highlight the role of TM4SF5 in forming protein complexes that regulate pathological processes.
Main Methods:
- Literature review focusing on TM4SF5.
- Analysis of protein-protein interactions involving TM4SF5.
- Examination of TM4SF5's role in cancer signaling pathways.
Main Results:
- TM4SF5 forms extensive protein complexes with various membrane proteins and cytosolic signaling molecules.
- Key interactions include those with integrins (α2, α5, β1), EGFR, IL6R, CD151, FAK, and c-Src.
- These interactions are crucial for regulating signaling activities during tumorigenesis and metastasis.
Conclusions:
- TM4SF5 plays a critical role in promoting cancer development and spread through complex formation and signaling modulation.
- Targeting TM4SF5-mediated interactions presents a potential therapeutic strategy for cancer treatment.
- Further research into these interactions can elucidate mechanisms of TM4SF5-driven cancer.
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