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辐射诱导的顺铂耐药性海拉细胞的克隆变异性

Clonal variability of radiation-induced cisplatin resistant HeLa cells.

作者信息

Eichholtz-Wirth H, Marx K

机构信息

GSF-National Research Center for Environment and Health, Institute of Radiology, Neuherberg, Germany.

出版信息

Anticancer Res. 1998 Jul-Aug;18(4C):2989-91.

PMID:9713497
Abstract

Low-dose fractionated gamma-irradiation (3 cycles of 5x2 Gy) induces moderate cisplatin resistance in HeLa cells which is associated with alterations of the caspase-dependent apoptotic pathway (2). There is a considerable heterogeneity in cell survival among isolated resistant clones (Rf values between 1.4 to 2.4) and in the propensity of the cells to enter apoptosis. These variations are associated with altered activation of the apoptotic pathway by members of the TNF family. The membrane receptor CD95 (Apo-1/Fas), which is upregulated immediately after cisplatin exposure in parental HeLa cells, is expressed at various levels in the resistant clones. There are also changes in the formation of the inhibitor protein I kappa B, which regulates the antiapoptotic transcription factor NF kappa B. Since the response to radiation is unchanged, the results collectively suggest that changes in the activation of the caspase-dependent signalling cascade are involved in the death pathway initiated by cisplatin but not by radiation damage.

摘要

低剂量分次伽马射线照射(3个周期,每次5×2 Gy)可诱导HeLa细胞产生中度顺铂耐药性,这与半胱天冬酶依赖性凋亡途径的改变有关(2)。在分离出的耐药克隆中,细胞存活率存在相当大的异质性(Rf值在1.4至2.4之间),且细胞进入凋亡的倾向也不同。这些差异与TNF家族成员对凋亡途径的激活改变有关。膜受体CD95(Apo-1/Fas)在亲本HeLa细胞中顺铂暴露后立即上调,在耐药克隆中表达水平各不相同。调节抗凋亡转录因子NF-κB的抑制蛋白IκB的形成也有变化。由于对辐射的反应未改变,这些结果共同表明,半胱天冬酶依赖性信号级联激活的变化参与了顺铂引发的死亡途径,但不参与辐射损伤引发的死亡途径。

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