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作 者:檀碧波[1] 李勇[1] 范立侨[1] 赵群[1] 刘羽[1] 赵雪峰[1]
机构地区:[1]河北医科大学第四医院外三科,石家庄050011
出 处:《中华实验外科杂志》2012年第7期1315-1317,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81072033);河北省自然科学基金资助项目(C2010000619);河北省普通高校强势特色学科资助项目[冀教高(2005)52];河北省卫生厅科研基金资助项目(20110460)
摘 要:目的探讨胃癌凋亡相关蛋闩表达与体外化疗药敏性的关系。方法对64例胃癌标本进行Survivin、B淋巴细胞/白血病-2(bcl-2)、bax免疫组织化学染色,并以噻唑蓝(MTF)比色法检测体外化疗药物敏感性。结果肿瘤Smwivin、bcl-2、bax阳性表达率分别为90.6%、75.0%、68.8%;Survivin与bax、bcl-2与bax间表达强度均呈负相关(r=-0.45044、-0.41403,P〈0.01)。在耐药因子表达程度与药物对肿瘤细胞抑制率的关系中,Smwivin强表达时,表阿霉素(eADM)、顺铂(DDP)对肿瘤细胞的抑制率明显降低(P〈0.05),但奥沙利铂(L—OHP)对肿瘤细胞的抑制率明显增加(P〈0.05);bcl-2强表达时,5-氟尿嘧啶(5-FIJ)、紫杉醇(PTX)、eADM对肿瘤细胞的抑制率明显低于弱表达组(P〈0.05);bax强表达组中,5-Fu、eADM、L—OHP和甲氨喋呤(MTX)对肿瘤细胞的抑制率明显高于弱表达组(P〈0.05)。结论胃癌凋亡相关蛋白表达与部分化疗药物敏感性有关。Objective To investigate the relationship between expression of apoptosis-related pro- teins and chemosensitivities in gastric carcinoma. Methods The expression levels of Survivin, B lympho- eytes/leukemia-2 (bcl-2) and bax were determined immunohistochemically, and the chemosenisitivities of 9 drugs were measured by methyl thiazol tetrazolium (MTT) assay in 64 tissue specimens of gastric carci- nomas. Results The positive rate of Survivin, bcl-2 and bax was 90. 6% , 75.0% and 68.8% respective- ly. There was negatively significant correlations between the expression of Survivin and bax, and bel-2 and bax (r = -0. 450 44, -0. 414 03, both P〈0. 01 ). In terms of relationship between the expression of Survivin, bcl-2, bax and inhibition rate of tumor cells, the inhibition rate for epirubicin (eADM) and cis- platin (DDP) in Survivin strong expression group was lower than that in weak group (both P 〈 0. 05 ), but for oxaliplatin (L-OHP) the inhibition rate was increased ( P 〈 0. 05 ). The inhibition rate to 5-fluorouraeil (5-Fu), paclitaxel (PTX) and eADM was significantly lower in the bcl-2 strong expression group than the weak group (all P 〈 0. 05). There was higher inhibition rate for 5-Fu, eADM, L-OHP and methotrexate (MTX) in bax strong expression group ( all P 〈 0. 05 ). Conclusion The expression of apoptosis-related proteins in gastric carcinoma was associated with the chemosensitivities of parts of drugs.
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