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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Expression of anti-apoptosis genes determines the response of adrenal cancer to apoptosis-inducing chemotherapy.
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Expression of anti-apoptosis genes determines the response of adrenal cancer to apoptosis-inducing chemotherapy.

机译:抗凋亡基因的表达决定了肾上腺癌对诱导凋亡的化学疗法的反应。

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摘要

BACKGROUND: This study tested the hypothesis that response of adrenal cortical carcinoma (ACC) to pro-apoptosis drugs depends on expression of anti-apoptosis genes. MATERIALS AND METHODS: Expression of Bcl-2 and Bcl-XL proteins was determined in two human adrenal cancer cell lines, NCI-H-295 and RL-251. Two pro-apoptosis drugs, gossypol (G) and docetaxel (D) were tested in vitro and in vivo in a human ACC/SCID mouse chimera. RESULTS: Bcl-XL was strongly expressed in RL-251 but not in H-295 and neither expressed the Bcl-2 protein. G and D induced greater dose-dependent inhibition of cell proliferation in RL-251 than in H-295 cells and completely suppressed growth of tumors with high expression of Bcl-XL (p<0.05) while there was no growth suppression in tumors without Bcl-XL expression. CONCLUSION: This study provided proof of concept that expression of Bcl-XL determines response to pro-apoptosis drugs. Profiling adrenal tumors for expression of anti-apoptosis genes may provide clues to their potential response to drugs that induce apoptosis.
机译:背景:这项研究检验了一种假设,即肾上腺皮质癌(ACC)对促凋亡药物的反应取决于抗凋亡基因的表达。材料与方法:在两种人肾上腺癌细胞系NCI-H-295和RL-251中测定Bcl-2和Bcl-XL蛋白的表达。在人ACC / SCID小鼠嵌合体中体外和体内测试了两种促凋亡药物棉酚(G)和多西他赛(D)。结果:Bcl-XL在RL-251中高表达,而在H-295中不表达,且均不表达Bcl-2蛋白。 G和D在RL-251中诱导的细胞增殖抑制作用大于H-295细胞,并完全抑制了高表达Bcl-XL的肿瘤的生长(p <0.05),而没有Bcl-XL的肿瘤则没有生长抑制作用-XL表达式。结论:这项研究提供了概念的证据,即Bcl-XL的表达决定了对促凋亡药物的反应。对肾上腺肿瘤进行分析以表达抗凋亡基因可能为它们对诱导凋亡的药物的潜在反应提供线索。

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