Polychlorinated biphenyls promote cell survival through pyruvate kinase M2-dependent glycolysis in HeLa cells.

Toxicol Mech Methods

a Institute of Biotechnology , Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan , China.

Published: July 2019

AI Article Synopsis

  • The study explores the effects of three specific polychlorinated biphenyls (PCBs) on the survival of human cervical cancer HeLa cells, revealing that these compounds significantly enhance cell survival over 48 hours.
  • Exposure to these PCBs led to increased glycolysis markers, such as elevated glucose consumption and lactate production, indicating that the chemicals stimulate the glycolytic pathway in cancer cells.
  • The findings suggest that the upregulation of glycolysis and enhanced cell survival in HeLa cells occur via a mechanism involving the protein PKM2 and ROS production, with potential for antioxidant treatments to counteract these effects.

Article Abstract

It is well known that polychlorinated biphenyls (PCBs) are typical persistent organic pollutants (POPs) in the environment. The present study investigated the effects of three PCBs including 3,3',4,4',5-pentachlorobiphenyl (PCB126), 2,3',4,4',5-pentachlorobiphenyl (PCB118), and 2,2',4,4',5,5'-hexachlorobiphenyl (PCB153) on human cervical carcinoma HeLa cell survival and the possible underlying mechanisms. The results showed that PCB126, PCB118, or PCB153 exposure for 48 h significantly promoted HeLa cell survival. Meanwhile, glucose consumption, lactate production, and glycolysis-related proteins including glucose transporter-1 (GLUT1), lactate dehydrogenase (LDHA), and pyruvate dehydrogenase kinase (PDK) were remarkably elevated after three PCBs treatment, indicated PCBs stimulating glycolysis. Moreover, we found that the expression and nuclear distribution of PKM2 protein was significantly increased in PCB126, PCB118, or PCB153-treated HeLa cells. However, the enzymatic activity of PKM2 was reduced. In addition, the three congeners exposure elevated ROS levels and the expression of NADPH oxidase subunits such as NOX2, p47, and p40. The addition of antioxidant NAC antagonized the three PCBs-induced effects on PKM2, cell survival, and glycolysis. Taken together, these results indicated that PCB126, PCB118, or PCB153 exposure promotes cervical cancer HeLa cell survival by PKM2-dependent upregulation of glycolysis, which is mediated by NADPH oxidase-induced ROS production.

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http://dx.doi.org/10.1080/15376516.2019.1584658DOI Listing

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