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作 者:彭光彩[1] 王晓雯[1] 易村犍[1] Peng Guangcai Wang Xiaowen Yi Cunjian(Department of Obstetrics and Gynecology, The First Affiliated Hospital of Yangtze University,Jingzhou 43430)
机构地区:[1]长江大学附属第一医院妇产科,荆州434300
出 处:《现代妇产科进展》2016年第12期891-894,899,共5页Progress in Obstetrics and Gynecology
摘 要:目的::监测卵巢癌患者外周血中游离干细胞因子( SCF)的浓度变化和c-kit蛋白在卵巢癌组织中的表达,探讨外周血SCF值对早期预测c-kit (+)上皮性卵巢癌继发性化疗耐药的临床价值。方法:利用量子点双染免疫荧光( QDs)检测106例卵巢癌组织中c-kit和SCF蛋白表达,ELISA法检测46例上述卵巢癌患者化疗期间冰冻保存的外周血SCF值,分析铂类为主的化疗药物敏感型和耐药型卵巢癌患者外周血SCF值与组织c-kit表达的差异。结果:继发性化疗耐药的上皮性卵巢癌组织中,c-kit(+)表达率远高于化疗敏感组(29.27% vs 10.8%,P<0.05),c-kit(+)表达率随着FIGO分期的进展而升高(Ⅰ~Ⅱ期8.7%,Ⅲ~Ⅳ期25%,P<0.05)。继发性化疗耐药组的外周血SCF值随铂类为主的化疗药物治疗而有升高的趋势,化疗敏感组的SCF值随之有下降的趋势;继发性化疗耐药组的外周血SCF均值高于化疗敏感组( P<0.05)。卵巢癌c-kit (+)的外周血SCF值均值高于c-kit(-)组(P=0.018),外周血SCF值在卵巢癌c-kit(+)组随铂类为主的化疗耐药而升高。结论:卵巢上皮癌组织中c-kit蛋白阳性表达可能导致肿瘤对铂类化疗药物耐药;c-kit蛋白在肿瘤间质细胞内的阳性表达,预示卵巢上皮性癌化疗耐药微环境的形成和极差的临床结局。卵巢癌化疗期间,监测外周血SCF值升高可能是早期预测c-kit(+)卵巢癌继发性化疗耐药的标记物之一。Objective:To monitor the changes in the concentration of free stem cell fac-tor ( SCF) in peripheral blood and the expression of c-kit protein in ovarian cancer tissues,and to investigate the clinical value of early prediction of c-kit (+) in epithelial ovarian cancer (EOC) resistance to platinum-based chemotherapy by monitoring SCF in peripheral blood. Methods:Expressions of c-kit and SCF were retrospectively studied with quantum dots immuno-fluorescence histochemistry ( QDs-IHC) ,in paraffin-embeded tissue specimens from 106 cases of EOC. The plasma concentration of the SCF were measured with enzyme linked immuno-sor-bent assay ( ELISA) from 46 EOC. To investigate the difference of SCF value in peripheral ser-um and c-kit expression of EOC patients who were sensitive and resistant to platinum-based chemotherapy. Results:In epithelial ovarian cancer ( EOC) ,the positive expression rate of c-kit in the chemoresistance group was 29. 27%,it was statistically higher than chemosensitive group (10. 8%)(P〈0. 05). The positive expression of c-kit in EOC was closely corralated with ad-vanced FIGO clinical stages and chemotherapy-sensitivity. The positive rate increased in ad-vanced stage (Ⅰ~Ⅱ8 . 7%,Ⅲ~Ⅳ25%) ( P〈0 . 05 ) . The mean plasma concentration of the SCF in the chemoresistance group was statistically higher than the chemosensitive group of EOC ( P〈0 . 05 ) . The plasma concentration of the SCF in the chemoresistance group was up-regula-ted after platinum-based chemotherapy. The mean value of the SCF in c-kit (+) group was higher than that in c-kit (-) group in epithelial ovarian cancer(P=0. 018),the plasma con-centration of the SCF in c-kit (+) group was up-regulated after platinum-based chemotherapy. Conclusion:The abnormal expression of c-kit protein may play an important role in the progres-sion and chemoresistance of EOC. The positive expression of c-kit protein in ovarian cancer stromal cell indicated poor clinical outcome
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