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作 者:刘殊[1] 冯丹[1] 刘云鹏[2] 侯柯佐[2] 于萍[2]
机构地区:[1]中国医科大学附属第四医院肿瘤内科,辽宁沈阳110032 [2]中国医科大学附属第一医院肿瘤内科,辽宁沈阳110001
出 处:《中华肿瘤防治杂志》2007年第6期430-432,共3页Chinese Journal of Cancer Prevention and Treatment
基 金:辽宁省自然科学基金(962303);辽宁省教育厅基金(20122152)
摘 要:目的:研究DNA-PKcs和Bcl-2在急性白血病(AL)细胞中的表达及相关性。方法:采用免疫组化SP法检测62名初治AL患者骨髓白血病细胞DNA-PKcs和Bcl-2的表达。结果:DNA-PKcs在对化疗药物耐药患者白血病细胞中的表达率(51.5%)明显高于敏感组(20.7%),P<0.05。Bcl-2在对化疗药物耐药患者白血病细胞中的表达率(84.8%)明显高于敏感组(62.1%),P<0.05。耐药组患者的白血病细胞中DNA-PKcs(+)/Bcl-2(+),DNA-PKcs(+)/Bcl-2(-),DNA-PKcs(-)/Bcl-2(+)和DNA-PKcs(-)/Bcl-2(-)细胞的百分率分别是88.2%,33.3%,44.8%和30.0%,DNA-PKcs(+)/Bcl-2(+)与DNA-PKcs(+)/Bcl-2(-)、DNA-PKcs(-)/Bcl-2(+)和DNA-PKcs(-)/Bcl-2(-)之间差异均有统计学意义(P<0.05,P<0.01,P<0.01)。33名耐药组患者中,DNA-PKcs和Bcl-2的表达无相关性,r=0.171,P>0.05。29名敏感组患者中,DNA-PKcs和Bcl-2的表达呈负相关,r=-0.45,P<0.05。结论:DNA-PKcs可能下调Bcl-2的表达,AL患者的白血病细胞中DNA-PKcs和Bcl-2表达水平增高与临床耐药密切相关。OBJECTIVE: To study the expressions of DNA-PKcs and Bcl-2 and their relationship in acute leukemia (AL) patients. METHODS: The expressions of DNA-PKcs and Bcl-2 in bone marrow mononuelear cells of 62 AL patients were measured by SP immunohistoehemistry method. RESULTS: The positive expression rate of DNA-PKcs in the treatment resistant group(51.5%)was significantly higher than that in the sensitive group(20.7 % ), P〈0.05. The positive expression rate of Bcl-2 in the treatment resistant group (84.8 %) was significantly higher than that in the sensitive group(62.1%),P〈 0.05. The percentage of patients with DNA-PKcs ( + )/Bcl-2 (+) in the treatment resistant group(88.2% ) was significantly higher than that of ones with DNA-PKcs (+)/Bcl-2 (-) (33.3%),DNA-PKcs(-)/Bcl-2(+)(44.8%) and DNA-PKcs (-)/Bcl-2(- )(30.0%), respectively(P〈0.05, P〈0.01, P〈0.01). In the treatment resistant group, there was no correlation between DNA-PKes and Bcl-2 expression, r= 0. 171, P〉0.05. However, in the treatment sensitive group, negative correlation existed between the expression of DNA-PKes and Bcl-2, r=0.45,P〈0.05. CONCLUSIONS: DNA-PKcs probably down-regulates Bcl-2 in triggering apoptosis in response to se vere DNA damage, and the higher expressions of DNA-PKcs and Bcl-2 are closely correlated with clinical drug resistance.
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