International Journal of Nanomedicine (Jan 2023)

Proteomics and Metabolomics Analysis Reveals the Toxicity of ZnO Quantum Dots on Human SMMC-7721 Cells

  • Yang Y,
  • Wang X,
  • Song Z,
  • Zheng Y,
  • Ji S

Journal volume & issue
Vol. Volume 18
pp. 277 – 291

Abstract

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Yanjie Yang, Xu Wang, Zhenhua Song, Yafei Zheng, Shaoping Ji Henan Provincial Engineering Center for Tumor Molecular Medicine, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, People’s Republic of ChinaCorrespondence: Shaoping Ji, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, People’s Republic of China, Tel +86 371 2388 0585, Fax +86 371 2388 0585, Email [email protected]: ZnO quantum dots (QDs) are composed of less toxic metals than other QDs but have the same interesting photochemical properties. Thus, they have received considerable attention recently. Nevertheless, their toxicity cannot be ignored.Methods: In this study, we incubated ZnO QDs with human SMMC-7721 cells for 24 h to assess their nanotoxicity through proteomics (Fold change > 1.5 and p-value < 0.05) and metabolomics (Fold change ≥ 1.5; VIP ≥ 1; p-value < 0.05) analyses.Results: Both of 174 and 219 significantly changed metabolites were identified in human SMMC-7721 cells treated with 20 and 50 μg/mL ZnO QDs, respectively. ZnO QDs significantly modified metabolic pathways, including purine metabolism, ferroptosis, morphine addiction, alcoholism, cGMP-PKG signaling, and Cushing syndrome. Moreover, we identified 105 and 8 differentially expressed proteins in cells treated with 20 and 50 μg/mL ZnO QDs, and the pathways of alcoholism and Cushing syndrome were enriched.Conclusion: ZnO QDs did not affect cell viability in a CCK8 assay, but disturbed the level of intracellular metabolites and proteins at 20 μg/mL. The KEGG analyses of the metabolomics and proteomics data both enriched the alcoholism and Cushing syndrome pathways. These results provide an experimental basis for future research on the safe use of nanomaterials.Keywords: ZnO quantum dots, cytotoxicity, proteomics, metabolomics

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