Using intracellular metabolic profiling to identify novel biomarkers of cisplatin-induced acute kidney injury in NRK-52E cells

• Published in: Journal of Toxicology and Environmental Health, Part A Part A, 2022-01, Vol.85 (1), p.29-42
• Main Authors: Kim, Hae Ri, Park, Jae Hyeon, Lee, Song Hee, Kwack, Seung Jun, Lee, Jaewon, Kim, Suhkmann, Yoon, Sungpil, Kim, Kyu-Bong, Lee, Byung Mu, Kacew, Sam, Kim, Hyung Sik
• Format: Article
• Language: English
• Subjects: acetate; Acetates - metabolism; Acetic acid; acute kidney injury; Acute Kidney Injury - chemically induced; Acute Kidney Injury - metabolism; Acute Kidney Injury - pathology; Animals; Apoptosis; Apoptosis - drug effects; BAX protein; Biocompatibility; biomarker; Biomarkers; Biomarkers - metabolism; Calbindin; Cell culture; Cell cycle; Cell Cycle - drug effects; Cell death; Cell Line; Chemotherapy; Cisplatin; Cisplatin - toxicity; Citric acid; Clusterin; Creatinine; Culture media; Cytotoxicity; Drug development; Gelatinase; In vivo methods and tests; Intracellular; Kidneys; Lactic acid; Leukocytes (neutrophilic); Lipocalin; Lysates; Metabolic pathways; Metabolism; Metabolites; Metabolomics; Models, Biological; nephrotoxicity; NMR; Nuclear magnetic resonance; p53 Protein; Proteins; Pyruvate kinase; Rats; Selenium; sirt1; Spectroscopy; Toxicity
• ISSN: 1528-7394; 1087-2620; 2381-3504
• DOI: 10.1080/15287394.2021.1969305

The aim of this study was to investigate changes in the intracellular metabolism resulting from cisplatin (CDDP)-induced nephrotoxicity in normal kidney tubular epithelial NRK-52E cells. Cytotoxicity, cell cycle analysis, and apoptotic cell death were all evaluated in NRK-52E cells treated with CDDP. Subsequently, proton nuclear magnetic resonance ( 1 H-NMR) spectroscopy was used to investigate cellular metabolic profiles. CDDP-induced nephrotoxicity was determined in vivo model. Cytotoxicity in the NRK-52E cells significantly rose following treatment with CDDP and these increases were found to be concentration-dependent. Both p53 and Bax protein expression was increased in CDDP-treated NRK-52E cells, correlating with enhanced cellular apoptosis. In addition, a number of metabolites were altered in both media and cell lysates in these cells. In cell lysates, citrate, creatinine, and acetate levels were dramatically reduced following treatment with 20 µM CDDP concentrations, while glutamate level was elevated. Lactate and acetate levels were significantly increased in culture media but citrate concentrations were reduced following high 20 µM CDDP concentrations incubation. In addition, excretion of clusterin, calbindin, neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), selenium binding protein 1 (SBP1), and pyruvate kinase M2 (PKM2) into the culture media was significantly increased in CDDP-treated cells while expression of acetyl CoA synthetase 1 (AceCS1) was markedly reduced in these cells. These findings suggest that acetate-dependent metabolic pathway may be a reliable and useful biomarker for detecting CDDP-induced nephrotoxicity. Taken together, data demonstrate that the discovery of novel biomarkers by metabolite profiling in target cells may contribute to the detection of nephrotoxicity and new drug development.