Prevention of carcinogen-induced oral cancers by polymeric black tea polyphenols via modulation of EGFR-Akt-mTOR pathway

• Published in: Scientific reports Vol. 12; no. 1; p. 14516
• Main Authors: Nimbalkar, Vaishnavi K., Gangar, Jeet, Shai, Saptarsi, Rane, Pallavi, Mohanta, Subham Kumar, Kannan, Sadhana, Ingle, Arvind, Mittal, Neha, Rane, Swapnil, Mahimkar, Manoj B.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 25.08.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 631/337; 631/449; 631/67; 692/700; AKT protein; Angiogenesis; Apoptosis; Black tea; Carcinogenesis; Carcinogens; Cell proliferation; Cyclin D1; DNA damage; Epidermal growth factor; Epidermal growth factor receptors; Humanities and Social Sciences; Hypoxia; multidisciplinary; Oral cancer; Polyphenols; Science; Science (multidisciplinary); Tea; TOR protein; Tumors; Vascular endothelial growth factor
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-18680-0

The overexpression of Epidermal Growth Factor Receptor (EGFR) and dysregulation of its downstream effector pathways are important molecular hallmarks of oral cancers. Present study investigates the chemopreventive potential of polymeric black tea polyphenols (PBPs)/thearubigins (TRs) in the hamster model of oral carcinogenesis as well as determine the effect of PBPs on EGFR and the molecular players in the EGFR pathway. In dose-dependent manner, pre and concurrent treatment with PBPs (1.5%, 5%, 10%) decreased the number and volume of macroscopic tumors as well as the number and area of microscopic lesions. Interestingly, at 10% dose of PBPs, no macroscopic or microscopic tumors were observed. We observed PBPs mediated dose-dependent decrease in oxidative DNA damage (8OHdG); inflammation (COX-2); proliferation (PCNA, Cyclin D1); expression of EGFR, and its downstream signaling kinases (pAkt, Akt, and mTOR); hypoxia (HIF1α) and angiogenesis (VEGF). There was also a PBPs mediated dose-dependent increase in apoptosis (Bax). Thus, our data clearly indicate that the observed chemopreventive potential of PBPs was due to modulation in the EGFR pathway associated with cell proliferation, hypoxia, and angiogenesis. Taken together, our results demonstrate preclinical chemopreventive efficacy of PBPs and give an insight into its mechanistic role in the chemoprevention of experimental oral cancer.