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DNA修复酶的药理学抑制对两种人类白血病细胞系中的端粒酶活性和细胞凋亡有不同的调节作用。

Pharmacological inhibition of DNA repair enzymes differentially modulates telomerase activity and apoptosis in two human leukaemia cell lines.

作者信息

Dubner D, del Rosario Pérez M, Michelin S, Bourguignon M, Moreau P, Carosella E D, Gisone P

机构信息

Autoridad Regulatoria Nuclear, Gerencia de Apoyo Científico Laboratorio de Radiopatología, Avenida del Libertador 8250 (C1429BNP) Buenos Aires, Argentina.

出版信息

Int J Radiat Biol. 2004 Aug;80(8):593-605. doi: 10.1080/09553000412331283506.

Abstract

PURPOSE

To investigate the effect of wortmannin and 3-aminobenzamide (3-AB) on telomerase activity and apoptosis in two human leukaemia cells.

MATERIALS AND METHODS

MOLT-4 (p53-wild type) and KG1a (p53-null) cells were irradiated with gamma-rays (3 Gy at 1.57 Gy min(-1)) and the effects of wortmannin and 3-AB were evaluated. Telomerase activity was measured by polymerase chain reaction and the expression of human telomerase reverse transcriptase, human telomerase RNA and telomerase-associated protein 1 was assessed by reverse transcriptase-polymerase chain reaction. Apoptosis was evaluated by fluorescence microscopy and flow cytometry.

RESULTS

A radiation-induced up-regulation of telomerase activity was observed from 4 h post-irradiation in both cell lines. This up-regulation was abrogated by wortmannin and 3-AB. Telomerase activity was maximal 24 h post-irradiation, coinciding with an accumulation of human telomerase reverse transcriptase mRNA. Apoptosis and G2/M arrest were evident from 4 h post-irradiation in MOLT-4 cells. KG1a cells exhibited a G2/M block at 24 h post-irradiation and apoptosis increased between 24 and 48 h post-irradiation. 3-AB abolished G2/M blockage and enhanced radiation-induced apoptosis in both cell lines, while wortmannin increased apoptosis only in MOLT-4 cells.

CONCLUSIONS

3-AB inhibits the radiation-associated telomerase activity increase and enhances apoptosis in MOLT-4 and KG1a cells. Wortmannin, which also inhibits the radiation-associated telomerase activity increase in both cell lines, does not modify radiation-induced apoptosis in KG1a cells. DNA repair enzymes might be selective targets for enhancing radiosensitivity in certain tumour cells.

摘要

目的

研究渥曼青霉素和3-氨基苯甲酰胺(3-AB)对两种人白血病细胞端粒酶活性及细胞凋亡的影响。

材料与方法

用γ射线(1.57 Gy/min,3 Gy)照射MOLT-4(p53野生型)和KG1a(p53缺失型)细胞,评估渥曼青霉素和3-AB的作用。通过聚合酶链反应测定端粒酶活性,用逆转录-聚合酶链反应评估人端粒酶逆转录酶、人端粒酶RNA和端粒酶相关蛋白1的表达。通过荧光显微镜和流式细胞术评估细胞凋亡。

结果

两种细胞系在照射后4小时均观察到辐射诱导的端粒酶活性上调。渥曼青霉素和3-AB可消除这种上调。端粒酶活性在照射后24小时达到最大值,与人端粒酶逆转录酶mRNA的积累一致。MOLT-4细胞在照射后4小时出现细胞凋亡和G2/M期阻滞。KG1a细胞在照射后24小时出现G2/M期阻滞,照射后24至48小时细胞凋亡增加。3-AB消除了两种细胞系的G2/M期阻滞并增强了辐射诱导的细胞凋亡,而渥曼青霉素仅增加了MOLT-4细胞的凋亡。

结论

3-AB抑制辐射相关的端粒酶活性增加并增强MOLT-4和KG1a细胞的凋亡。渥曼青霉素也抑制两种细胞系中辐射相关的端粒酶活性增加,但不改变KG1a细胞中辐射诱导的细胞凋亡。DNA修复酶可能是增强某些肿瘤细胞放射敏感性的选择性靶点。

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