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热疗、多胺耗竭与X射线诱导的DNA链断裂修复抑制

Hyperthermia, polyamine depletion, and inhibition of X-ray-induced DNA strand break repair.

作者信息

Snyder R D, Lachmann P J

机构信息

Merrell Dow Research Institute, Cincinnati, Ohio 45215.

出版信息

Radiat Res. 1989 Oct;120(1):121-8.

PMID:2798775
Abstract

We have recently demonstrated that HeLa cells that had been depleted of polyamines by treatment with inhibitors of polyamine biosynthesis were deficient in their ability to repair X-ray-induced DNA strand breaks. Since it had previously been demonstrated that hyperthermic shock also inhibited strand break repair following X irradiation and that hyperthermia resulted in a leakage of polyamines from cells, it seemed of interest to examine whether the inhibition of repair by hyperthermia was related to this loss of cellular polyamines. In the present paper it is demonstrated that both polyamine depletion and hyperthermia inhibit strand closure, and that a combined treatment further reduces the rate of repair. In cells not depleted of polyamines, repair is restored to normal levels if hyperthermia treatment is followed by a 4-h incubation at 37 degrees C before X irradiation. In polyamine-depleted cells, this 37 degrees C incubation does not result in a return of repair ability. Polyamine supplementation was not effective in reversing hyperthermia-dependent repair inhibition, and, in fact, restoration of repair in control cells following hyperthermic shock corresponded to a time at which polyamines show a maximum decrease in those cells. These results suggest that the inhibition of repair and the increased radiosensitivity observed in hyperthermically treated cells is not related to polyamine depletion. However, data further suggest that polyamine-depleted cells may have other alterations, perhaps in chromatin, which render them more sensitive to thermal inhibition of repair.

摘要

我们最近证明,用多胺生物合成抑制剂处理后耗尽多胺的HeLa细胞修复X射线诱导的DNA链断裂的能力存在缺陷。由于此前已证明热休克也会抑制X射线照射后的链断裂修复,且热休克会导致细胞内多胺泄漏,因此研究热休克对修复的抑制是否与细胞内多胺的这种损失有关似乎很有意义。在本文中,我们证明多胺耗尽和热休克都会抑制链封闭,并且联合处理会进一步降低修复速率。在未耗尽多胺的细胞中,如果在X射线照射前,热休克处理后在37℃孵育4小时,修复会恢复到正常水平。在多胺耗尽的细胞中,这种37℃孵育并不会导致修复能力恢复。补充多胺对逆转热休克依赖的修复抑制无效,事实上,热休克后对照细胞修复的恢复与多胺在这些细胞中显示最大减少的时间相对应。这些结果表明,在热休克处理的细胞中观察到的修复抑制和放射敏感性增加与多胺耗尽无关。然而,数据进一步表明,多胺耗尽的细胞可能有其他改变,也许在染色质中,这使它们对热诱导的修复抑制更敏感。

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