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12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯及其与叙利亚和中国仓鼠细胞中姐妹染色单体互换诱导的关系。

12-O-tetradecanoyl-phorbol-13-acetate and its relationship to SCE induction in Syrian and Chinese hamster cells.

作者信息

Popescu N C, Amsbaugh S C, Larramendy M L, DiPaolo J A

出版信息

Environ Mutagen. 1982;4(1):73-81. doi: 10.1002/em.2860040110.

Abstract

12-O-Tetradecanoyl-phorbol-13-acetate (TPA) in conditions that produce enhancement of ultraviolet light (UV) and x-irradiation Syrian hamster embryo cell (HEC) transformation did not cause further increase in the sister chromatid exchange (SCE) frequency induced by UV and x-irradiation, two physical carcinogens that differ in their mode of DNA interaction and efficiency of SCE induction. Several factors which might influence SCE induction by TPA were studied on HEC and Chinese hamster V79-4 cells. Heat-inactivated serum was used because of the possibility that a serum component may interfere with TPA ability to cause SCE. TPA effect on SCE was determined at the first and second division post treatment on cells exposed to different 5-bromodeoxyuridine (BrdUrd) concentrations. Independent of BrdUrd concentration (1-10 microgram/ml medium) and the number of cell divisions post treatment TPA (0.01-2 microgram/ml medium) was ineffective in inducing SCE in exponentially and stationary HEC cultures cultivated in medium supplemented with heat-inactivated serum. Also, TPA did not increase the SCE frequency in V79-4 Chinese hamster cells cultured in heat-inactivated or noninactivated serum. Although SCE induction, a cellular response to carcinogen-induced DNA damage, may be important for the induction of transformation by environmental agents, the enhancement of transformation frequency caused by TPA occurs without further DNA alterations involved in SCE formation.

摘要

在能增强紫外线(UV)和X射线对叙利亚仓鼠胚胎细胞(HEC)转化作用的条件下,12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)并不会导致由UV和X射线诱导的姐妹染色单体交换(SCE)频率进一步增加,这两种物理致癌物在DNA相互作用模式和SCE诱导效率方面存在差异。在HEC和中国仓鼠V79 - 4细胞上研究了几种可能影响TPA诱导SCE的因素。使用热灭活血清是因为血清成分可能干扰TPA引起SCE的能力。在暴露于不同5 - 溴脱氧尿苷(BrdUrd)浓度的细胞处理后的第一次和第二次分裂时,测定TPA对SCE的影响。无论BrdUrd浓度(1 - 10微克/毫升培养基)和处理后细胞分裂次数如何,TPA(0.01 - 2微克/毫升培养基)在添加热灭活血清的培养基中培养的指数生长和静止期HEC培养物中诱导SCE均无效。此外,TPA在热灭活或未灭活血清中培养的V79 - 4中国仓鼠细胞中也不会增加SCE频率。虽然SCE诱导是细胞对致癌物诱导的DNA损伤的一种反应,可能对环境因子诱导转化很重要,但TPA引起的转化频率增加是在不涉及SCE形成的进一步DNA改变的情况下发生的。

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