The cytotoxic mechanism of epigallocatechin gallate on proliferative HaCaT keratinocytes

• Published in: Journal of biomedical science 2017-08, Vol.24 (1), p.55-55, Article 55
• Main Authors: Chu, Yu-Wen, Liu, Shu-Ting, Yang, Ya-Lan, Huang, Shih-Ming, Wang, Wei-Ming
• Format: Article
• Language: English
• Subjects: Antineoplastic Agents - pharmacology; Apoptosis; Calcium; Cancer; Catechin; Catechin - analogs & derivatives; Catechin - pharmacology; Cell culture; Cell cycle; Cell Line; Cell proliferation; Cells, Cultured; Chondrocytes; Condyloma acuminatum; Condylomata Acuminata - drug therapy; Condylomata Acuminata - virology; Cyclin D1; Cyclin-dependent kinases; Cytometry; Cytotoxicity; Differentiation; Epigallocatechin gallate; Epigallocatechin-3-gallate; Experiments; External genital warts; Flow cytometry; Gene expression; Growth; Health aspects; Homeostasis; HPV; Human papillomavirus; Humans; Infections; Keratinocytes; Kinases; Ointments; Papillomaviridae - drug effects; Papillomavirus Infections - drug therapy; Papillomavirus Infections - virology; Phagocytosis; Phosphorylation; Polymerase chain reaction; Proliferation; Proteins; Warts; Western blotting; Zinc; Zinc finger proteins
• ISSN: 1423-0127; 1021-7770; 1423-0127
• DOI: 10.1186/s12929-017-0363-7

Epigallocatechin gallate (EGCG) is the major ingredient of sinecatechins ointment, approved for the treatment of external genital and perianal warts. However, the molecular mechanism for EGCG's effect on warts resulting from the human papillomavirus (HPV) infection of keratinocytes is not well understood. HPV may survive in proliferative keratinocytes and may be involved in cell cycle regulation and progression. The objective of this study was to investigate the mechanism underlying EGCG's treatment on external genital warts of HPV infection through the cultured keratinocyte cells from the HaCaT cell line. MTT and flow cytometry assays were used to measure cell viability and the cell cycle profile, with and without EGCG treatment, for HaCaT keratinocyte cells cultured in a calcium-free medium and 1.8 mM calcium which induced proliferative and differentiated keratinocytes, respectively, for 24 h. The expression levels of cytotoxic proteins and factors were evaluated with the RT-PCR and western blotting analysis. EGCG influenced the proliferation stage but not the differentiation stage of keratinocytes. We suggest that apoptosis and autophagy might be the possible mechanism for the EGCG's effect on the proliferative HaCaT cells. Furthermore, we found that EGCG reduced the protein levels of cyclin D1 and Zac1 (a zinc-finger protein which regulates apoptosis and cell cycle arrest 1) dose-dependently in proliferative as compared to differentiated keratinocytes. It also induced the expression of p21 and DEC1 (differentiated embryo-chondrocyte expressed gene 1), and promoted G1 arrest of cell cycle in proliferative keratinocytes. These results help clarify the mechanisms of EGCG treatment of HPV-infected keratinocytes and may contribute to new targets, such as Zac1 and DEC1 for external genital and perianal warts.