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KPV peptide has emerged as a promising therapeutic candidate in the field of oncology, particularly due to its unique anti-inflammatory and immunomodulatory properties that can influence tumor microenvironments. While much of the early research focused on inflammatory bowel disease and skin conditions, recent studies suggest that KPV may also exert significant effects on cancer cells and the surrounding stroma. Understanding how this tripeptide interacts with inflammation pathways, its preclinical evidence in oncology, and its specific actions within the intestinal tract provides a comprehensive view of its potential as an adjunct or primary therapy for various cancers.
Exploring KPV Peptide and Inflammation
KPV is a short synthetic peptide composed of lysine (K), proline (P) and valine (V). Its anti-inflammatory activity was first noted in models of ulcerative colitis, where it inhibited neutrophil infiltration and cytokine release. The mechanism involves blocking the binding of chemokines to their receptors on immune cells, thereby reducing the recruitment of inflammatory mediators that often create a tumor-promoting milieu. In cancer biology, chronic inflammation is known to drive DNA damage, angiogenesis, images.google.td and metastatic potential
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