Oxidative stress and metabolic reprogramming in Cr(VI) carcinogenesis
Autor: | Xianglin Shi, Zhuo Zhang, Marco Clementino |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Glutaminolysis Cell growth Chemistry Tumor initiation Oxidative phosphorylation Pentose phosphate pathway Toxicology medicine.disease_cause Article Cell biology 03 medical and health sciences 030104 developmental biology 0302 clinical medicine 030220 oncology & carcinogenesis medicine Metal Carcinogenesis Carcinogenesis Oxidative stress |
Zdroj: | Current Opinion in Toxicology. 8:20-27 |
ISSN: | 2468-2020 |
DOI: | 10.1016/j.cotox.2017.11.015 |
Popis: | Cr(VI)-containing compounds are well-established lung carcinogens. Chronic exposure of the normal human epithelial cells is able to induce malignant cell transformation, the first stage of metal carcinogenesis. These Cr(VI)-transformed cells exhibit increased level of antioxidants, reduced capacity of generating reactive oxygen species (ROS), and development of apoptosis resistance, promoting tumorigenesis of Cr(VI)-transformed cells, the second stage of metal carcinogenesis. The mechanism of Cr(VI) induced carcinogenesis is still under investigation. Recent studies indicate that ROS play a positive role in the first stage while a negative role in the second stage. Transformed cells adapt metabolism to support tumor initiation and progression. Altered metabolic activities directly participate in the process of cell transformation or support a large requirement for nucleotides, amino acids, and lipids for tumor growth. In malignantly Cr(VI)-transformed cells, mitochondrial oxidative phosphorylation is defective, and pentose phosphate pathway, glycolysis, and glutaminolysis are upregulated. These metabolic reprogramming supports rapid cell proliferation and contributes to tumorigenesis of Cr(VI)-transformed cells. This article summarizes the current progress in the studies of metabolic reprogramming and Cr(VI) carcinogenesis with emphasis on the metabolic enzymes and oxidative stress related major oncogenic pathways. |
Databáze: | OpenAIRE |
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