1. Topotecan induces hepatocellular injury via ASCT2 mediated oxidative stress
- Author
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Zhou Guoliang, Jianting Yang, Hao Yu, Mei-song Qin, and Xiao-lin Zhang
- Subjects
0301 basic medicine ,Amino Acid Transport System ASC ,endocrine system diseases ,Glutamine ,Apoptosis ,medicine.disease_cause ,Minor Histocompatibility Antigens ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Western blot ,Cell Line, Tumor ,medicine ,Humans ,Cell Proliferation ,chemistry.chemical_classification ,Reactive oxygen species ,Hepatology ,medicine.diagnostic_test ,business.industry ,Cell growth ,Gastroenterology ,Glutathione ,Hep G2 Cells ,General Medicine ,Molecular biology ,Oxidative Stress ,030104 developmental biology ,chemistry ,030220 oncology & carcinogenesis ,Hepatocytes ,Topotecan ,Chemical and Drug Induced Liver Injury ,Topoisomerase I Inhibitors ,business ,Reactive Oxygen Species ,Oxidative stress ,medicine.drug - Abstract
Background Topotecan is an anti-cancer chemotherapy drug with common side effects, including hepatotoxicity. In this study, we aim to investigate the mechanisms of topotecan-induced hepatocellular injury beyond conventional DNA damage. Materials and methods Methyl Thiazolyl Tetrazolium (MTT) assay was used to detect the inhibitory effect of topotecan on cell proliferation. Western blot was used to detect protein expression. Flow cytometry assay was performed to determine apoptosis rate under topotecan treatment. ASCT2 overexpression was addressed using adenovirus vector. qRT-PCR and western blot assay were used to detect the expression of ASCT2. Glutamine uptake, intracellular glutathione (GSH) and reactive oxygen species (ROS) level were detected by glutamine detection kit, GSH detection kit and ROS detection kit respectively. Results MTT results showed that topotecan had an inhibitory effect on cell proliferation and induced apoptosis in both L02 and HepG2 cell lines. Topotecan inhibited the expression of glutamine transporter ASCT2 and the uptake of glutamine in both L02 and HepG2 cell lines. The uptake of glutamine and the GSH level was increased in both L02 and HepG2 cell lines after ASCT2 overexpression. The ROS level was inhibited by ASCT2 overexpression upon topotecan treatment in both L02 and HepG2 cell lines. Topotecan-induced hepatocellular apoptosis and proliferation inhibition were attenuated by ASCT2 overexpression in both L02 and HepG2 cell lines. Conclusion Topotecan-induced hepatocytes death is dependent on ASCT2 down-regulation, which causes oxidative stress via inhibiting GSH production.
- Published
- 2021
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