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Programming of Cell Resistance to Genotoxic and Oxidative Stress.
Velegzhaninov, Ilya O; Ievlev, Vitaly A; Pylina, Yana I; Shadrin, Dmitry M; Vakhrusheva, Olesya M.
Afiliação
  • Velegzhaninov IO; Institute of Biology of Komi Science Centre of Ural Branch of RAS, Syktyvkar 167982, Russia. vellio@yandex.ru.
  • Ievlev VA; Polytechnical Institute of Vyatka State University, Kirov 610000, Russia. vellio@yandex.ru.
  • Pylina YI; Biology department of St. Olaf College, Northfield, MN 55057, USA. ievlev1@stolaf.edu.
  • Shadrin DM; Institute of Biology of Komi Science Centre of Ural Branch of RAS, Syktyvkar 167982, Russia. yanapylina@yandex.ru.
  • Vakhrusheva OM; Institute of Biology of Komi Science Centre of Ural Branch of RAS, Syktyvkar 167982, Russia. shdimas@yandex.ru.
Biomedicines ; 6(1)2018 Jan 02.
Article em En | MEDLINE | ID: mdl-29301323
ABSTRACT
Different organisms, cell types, and even similar cell lines can dramatically differ in resistance to genotoxic stress. This testifies to the wide opportunities for genetic and epigenetic regulation of stress resistance. These opportunities could be used to increase the effectiveness of cancer therapy, develop new varieties of plants and animals, and search for new pharmacological targets to enhance human radioresistance, which can be used for manned deep space expeditions. Based on the comparison of transcriptomic studies in cancer cells, in this review, we propose that there is a high diversity of genetic mechanisms of development of genotoxic stress resistance. This review focused on possibilities and limitations of the regulation of the resistance of normal cells and whole organisms to genotoxic and oxidative stress by the overexpressing of stress-response genes. Moreover, the existing experimental data on the effect of such overexpression on the resistance of cells and organisms to various genotoxic agents has been analyzed and systematized. We suggest that the recent advances in the development of multiplex and highly customizable gene overexpression technology that utilizes the mutant Cas9 protein and the abundance of available data on gene functions and their signal networks open new opportunities for research in this field.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Federação Russa

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Federação Russa