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蝎毒联合ADM对人乳腺癌MCF-7细/胞的凋亡诱导作用及其耐药逆转的研究 被引量:4

Effect of Inducing Apoptosis and Resistance Reversing of BMK Combined with ADM on Human Breast Cancer MCF-7/ADM Cell Line
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摘要 目的探讨蝎毒(BMK)联合阿霉素(ADM)对人乳腺癌MCF-7/ADM细胞的凋亡诱导及其耐药逆转作用。方法MTT法、荧光分光光度法、流式细胞术、紫外分光光度术和免疫细胞化学法。结果①非细胞毒性剂量(3.0μg/m l)蝎毒能显著降低MCF-7/ADM的IC50(P<0.01),增加MCF-7/ADM细胞内ADM的药物积累(P<0.01)。②蝎毒(3.0μg/m l)联合ADM后增强了对耐药细胞的凋亡诱导作用,凋亡率由8.9±0.01%上升为12.6±0.21%(P<0.01)。③蝎毒(3.0μg/m l)能够显著降低耐药细胞内谷胱甘肽S转移酶(GSTs)酶的活性(P<0.01)。结论蝎毒能够部分逆转人乳腺癌MCF-7/ADM细胞对阿霉素的耐药性,其逆转机制与抑制耐药细胞GSTs活性有关。 Objective To study the effect of inducing apoposis and resistance reversing of buthus martensii karsch(BMK) combined with adriamycin (ADM) on human breast cancer MCF-7/ADM cell line. Methods The MTT assay, fluorescent-spectrophotometry, flow cytometry, UV-spectropbotometry and immunocytochemistry were used. Results ①The non-cytotoxic dose of BMK (μg/ml) significantly decreased the IC50 value of ADM and increased the intracellular ADM accumulation in MCF-7/ADM cells ( P 〈 0.01, P 〈 0.05 ). ②BMK(3μg/ml) combined with ADM increased the apoptosis inducing effect of ADM to MCF-7/ADM cells, which of apoptosis percentage was increased from (8.9 ± 0.01 ) % to ( 12.6 ± 0.21 ) % ( P 〈 0.01 ). ③BMK (3μg/ml) significantly decreased glutathione-S-transferase (GFTs) activity in MCF-7/ADM cells( P 〈0.01 ). Conclusion BMK could partially reverse resistance to ADM in human breast cancer MCF-7/ADM cell line, which may be associated with the decreased GSTs activity.
出处 《解剖科学进展》 CAS 2006年第3期224-226,共3页 Progress of Anatomical Sciences
关键词 蝎毒 耐药逆转 谷胱甘肽S转移酶 MCF-7/ADM细胞株 buthus martensii karsch resistane reverse MCF-7/ADM cell line glutathione-S-transferase
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