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Rahmanabadi et al

Therefore, while circulating formate levels were unable to discriminate between healthy participants and patients with pancreatic cancer, our data suggest that tracking formate levels over time in individuals could yield a biomarker for pancreatic cancer progression

Matthew Pincus and colleagues at the State University of New York (SUNY) Downstate Medical Center, combining two functional domains into a single 32-residue sequence: The HDM-2-binding domain p53 residues 1226, derived from the amino-terminal transactivation domain of the p53 tumour suppressor protein that naturally binds to HDM-2 (human double minute 2, also known as MDM2) A transmembrane-penetrating (membrane residency) peptide (MRP) derived from the Antennapedia homeodomain, fused to the C-terminus to enable membrane interaction and insertion upon target engagement What makes PNC-27 unique among anticancer research peptides is its proposed mechanism of action rather than triggering intracellular apoptosis pathways (the mechanism of most conventional chemotherapeutic approaches), PNC-27 targets HDM-2 expressed on the outer plasma membranes of cancer cells, forming transmembrane pores that cause rapid necrotic cell death through a process researchers have termed poptosis (peptide-induced transmembrane pore formation)

Furthermore, marmelosin exhibits potent antioxidant properties by enhancing endogenous antioxidant enzymes, including SOD, GSH, and CAT, thereby reducing oxidative stress, a key factor in the development of insulin resistance and -cell dysfunction

Harnessing Biomedical Applications of Ascorbic Acid, Berberine, and Glutathione-Capped Quantum Dots Through Multifunctional Physico-chemical, Biochemical, and Anti-microbial Assays

doi: 10.3389/fimmu.2024.1439176 139 ImdadAPanditNGZamanMMinkoffNZTanner-SmithEEGomez-DuarteOGet al