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The **rearranged during transfection receptor (RET)** is a receptor tyrosine kinase that plays a critical role in signal transduction pathways regulating cell proliferation, differentiation, survival, and migration. Germline and somatic activating mutations or gene fusions involving RET are oncogenic drivers in medullary thyroid carcinoma, papillary thyroid cancer, and other malignancies. RET is the therapeutic target of multiple tyrosine kinase inhibitors, including vandetanib, which selectively inhibits its kinase activity to block tumor cell growth, invasion, and angiogenesis, especially in advanced medullary thyroid cancer.
Inhibition of RET receptor tyrosine kinase activity; Blockade of downstream signal transduction pathways (e.g., Rho-GTPase/JNK, PI3K, MAPK); Inhibition of tumor growth, angiogenesis, and metastasis through suppression of RET-mediated signals.
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