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Association of elevated reactive oxygen species and hyperthermia induced radiosensitivity in cancer stem-like cells.


ABSTRACT: Cancer stem-like cells (CSCs) are the principal causes of tumor radio-resistance, dormancy and recurrence after radiotherapy. Clinical trials show hyperthermia (HT) might be a potent radiation sensitizer. In this study, CSCs were found to be more susceptible to radiation when combined with HT treatment. Treated cells showed significantly reduced self-renewal, cell survival and proliferation in vitro, as well as significant reduced tumor formation in vivo. Further study demonstrated that the radiosensitization effect was associated with increased intracellular reactive oxygen species (ROS) level in CSCs, confirmed by modifying redox status in CSCs bidirectionally. Pharmacologic depletion of glutathione by buthionine sulphoximine mimicked HT induced radiosensitivity in CSCs. Antioxidant N-acetylcysteine could efficiently rescue HT induced radiosensitivity in CSCs. To our knowledge, this may be the first report suggesting the association between elevated intracellular ROS level and HT induced radiosensitization in human breast CSCs and pancreatic CSCs, which might provide new strategy for improving CSCs radiosensitivity.

SUBMITTER: Fu Q 

PROVIDER: S-EPMC5731896 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Association of elevated reactive oxygen species and hyperthermia induced radiosensitivity in cancer stem-like cells.

Fu Qibin Q   Huang Tuchen T   Wang Xudong X   Lu Chunyang C   Liu Feng F   Yang Gen G   Wang Yugang Y   Wang Biao B  

Oncotarget 20171009 60


Cancer stem-like cells (CSCs) are the principal causes of tumor radio-resistance, dormancy and recurrence after radiotherapy. Clinical trials show hyperthermia (HT) might be a potent radiation sensitizer. In this study, CSCs were found to be more susceptible to radiation when combined with HT treatment. Treated cells showed significantly reduced self-renewal, cell survival and proliferation <i>in vitro</i>, as well as significant reduced tumor formation <i>in vivo</i>. Further study demonstrated  ...[more]

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