Department of Pulmonary Medicine, Medizinsche Klinik-Innenstadt, Ludwi-Maximilians-University, Munich, Germany.
Eur J Med Res. 2010 Oct 25;15(10):448-51. doi: 10.1186/2047-783x-15-10-448.
Resistance to cisplatin in the course of chemotherapy contributes to the poor prognosis of small cell lung cancer (SCLC). B cell lymphoma-2 is the founding member of a large family of proteins that either promote or inhibit apoptosis. We aimed at investigating if the pro-apoptotic members Bad, Bax, Bim and Bid are involved in cisplatin-resistance. - Cisplatin-resistance in the SCLC cell line H1339 was induced by repetitive exposure to cisplatin. Protein expression was quantified by Western Blot and immuno-fluorescence analysis. Protein expression was altered using siRNA interference. - Four cycles of 0.5 μg/ml cisplatin led to partial cisplatin-resistance in H1339 cells. The expression of Bad, Bim and Bid was comparable in naive and resistant cells while the expression of Bax was reduced in the resistant clone. But, reducing Bax expression in naive cells did not lead to altered cisplatin sensitivity neither in H1339 nor in H187 SCLC cells. - We conclude that the reduced Bax expression after exposure to cisplatin is not sufficient to induce cisplatin-resistance in SCLC cells.
在化疗过程中对顺铂的耐药性导致小细胞肺癌 (SCLC) 的预后不良。B 细胞淋巴瘤-2 是一大类蛋白的创始成员,这些蛋白可以促进或抑制细胞凋亡。我们旨在研究促凋亡蛋白 Bad、Bax、Bim 和 Bid 是否参与顺铂耐药性。-通过重复暴露于顺铂,在 SCLC 细胞系 H1339 中诱导顺铂耐药性。通过 Western Blot 和免疫荧光分析定量蛋白质表达。使用 siRNA 干扰改变蛋白质表达。-经过四轮 0.5μg/ml 顺铂处理,H1339 细胞中出现部分顺铂耐药性。在未处理和耐药细胞中,Bad、Bim 和 Bid 的表达水平相当,而 Bax 的表达在耐药克隆中降低。但是,降低未处理细胞中的 Bax 表达水平不会导致 H1339 和 H187 SCLC 细胞对顺铂的敏感性发生改变。-我们得出结论,暴露于顺铂后 Bax 表达的降低不足以诱导 SCLC 细胞的顺铂耐药性。