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Transmembrane protein 52B (TMEM52B) is a single-pass type I membrane protein, mainly located in the plasma membrane and extracellular exosomes. This protein is widely expressed in normal human tissues, with high levels in the kidney. TMEM52B plays a key role in modulating E-cadherin stability and cell–cell adhesion, supporting epithelial integrity. Experimental and clinical data indicate TMEM52B functions as a tumor suppressor, where decreased TMEM52B expression correlates with increased tumor invasion, enhanced signaling of downstream effectors such as β-catenin and EGFR, and poor clinical prognosis in cancers like colorectal and renal cell carcinoma. Research shows that TMEM52B-derived peptides can suppress cancer cell survival, anchorage-independent growth, and metastasis, highlighting its potential as both a therapeutic target and a prognostic biomarker in oncology.
In experimental models, TMEM52B-derived peptides inhibit tumor progression by stabilizing E-cadherin, reducing soluble E-cadherin, and interfering with EGFR activation
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