Heat Meets DNA: DNA Damage and Repair

Y. Nakagawa, A. Kajihara, T. Kirita, Eiichiro Mori
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引用次数: 3

Abstract

Hyperthermia is generally used in combination with chemo and radiation therapy in the treatment of various cancers. Thus far, most studies have focused on the additive effects of heat shock. However, it is also critical to understand the solitary effect of heat shock stress on mammalian cells. DNA double-strand breaks (DSBs) are known to be generated by ionizing radiation and a variety of DNA modifying reagents. As shown by neutral comet assays and γH2AX (phosphorylated histone H2AX at serine 139) focus formation, heat shock also induces DSBs. While existing literature suggests that heat shock leads to cell death through the induction of DSBs, the pathway involved in repairing heat-induced damage remains to be elucidated. In the current review, we examined the history of hyperthermia, from the discovery of DSBs after heat shock, to our recent finding regarding the homologous recombination repair pathway after heat shock.
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热与DNA相遇:DNA损伤与修复
热疗通常与化疗和放疗联合使用,用于治疗各种癌症。迄今为止,大多数研究都集中在热休克的加性效应上。然而,了解热休克应激对哺乳动物细胞的孤立效应也是至关重要的。DNA双链断裂(DSBs)是由电离辐射和各种DNA修饰试剂产生的。中性彗星实验和γ - H2AX(丝氨酸第139位磷酸化组蛋白H2AX)焦点的形成表明,热休克也会诱导dsb。虽然现有文献表明热休克通过诱导dsb导致细胞死亡,但修复热损伤的途径仍有待阐明。在当前的综述中,我们研究了热疗的历史,从热休克后dsb的发现,到我们最近关于热休克后同源重组修复途径的发现。
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