Dubner D, del Rosario Pérez M, Michelin S, Bourguignon M, Moreau P, Carosella E D, Gisone P
Autoridad Regulatoria Nuclear, Gerencia de Apoyo Científico Laboratorio de Radiopatología, Avenida del Libertador 8250 (C1429BNP) Buenos Aires, Argentina.
Int J Radiat Biol. 2004 Aug;80(8):593-605. doi: 10.1080/09553000412331283506.
To investigate the effect of wortmannin and 3-aminobenzamide (3-AB) on telomerase activity and apoptosis in two human leukaemia cells.
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.
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.
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.
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。
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。
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。
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。