Cell proliferation and carcinogenesis: an approach to screening for potential human carcinogens

被引:1
作者
Cohen, Samuel M. [1 ,2 ]
机构
[1] Univ Nebraska Med Ctr, Dept Pathol Microbiol & Immunol, Omaha, NE 68182 USA
[2] Univ Nebraska Med Ctr, Buffett Canc Ctr, Omaha, NE 68182 USA
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
two-year bioassay; mutagenesis; immunosuppression; estrogenic activity; cytotoxicity; regenerative proliferation; cell proliferation; CANCER-RISK; HUMAN RELEVANCE; IPCS FRAMEWORK; DOSE-RESPONSE; MODE; PANCREAS; BLADDER; LESIONS; TUMORS; INFORMATION;
D O I
10.3389/fonc.2024.1394584
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer arises from multiple genetic errors occurring in a single stem cell (clonality). Every time DNA replicates, mistakes occur. Thus, agents can increase the risk of cancer either by directly damaging DNA (DNA-reactive carcinogens) or increasing the number of DNA replications (increased cell proliferation). Increased cell proliferation can be achieved either by direct mitogenesis or cytotoxicity with regenerative proliferation. Human carcinogens have a mode of action of DNA reactivity, immunomodulation (mostly immunosuppression), increased estrogenic activity (mitogenesis), or cytotoxicity and regeneration. By focusing on screening for these four effects utilizing in silico, in vitro, and short-term in vivo assays, a biologically based screening for human chemical carcinogens can be accomplished with greater predictivity than the traditional 2-year bioassay with considerably less cost, less time, and the use of fewer animals.
引用
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页数:7
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