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MIEN1-derived peptides (specifically LA3IK and RP-7) are first-in-class anticancer peptides derived from the conserved immunoreceptor tyrosine-based activation motif (ITAM) and prenylation motif sequences of the Migration and Invasion Enhancer 1 (MIEN1) protein, a cancer-specific oncogene overexpressed in multiple aggressive cancers including breast and prostate cancer. These therapeutic peptides act as dominant-negative inhibitors of the MIEN1 signaling pathway, disrupting cancer cell migration, invasion, and epithelial-to-mesenchymal transition (EMT). LA3IK, a hexamer peptide, has also been shown to selectively disrupt EGFR–ERBB2 heterodimerization, reducing downstream NF-κB, Src, and STAT3 signaling. D-isomer analogs (such as D-LA3IK and D-RP-7) have been developed to improve metabolic stability and bioavailability. The compounds are in preclinical development by researchers at the University of North Texas Health Science Center.
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