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TCRP1通过PI3k-Akt途径介导口腔鳞癌顺铂化学治疗耐受

TCRP1 mediates the resistance of oral squamous cell carcinoma to cisplatin through regulation of PI3K–Akt pathway

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【作者】 谷依学王成昆尹江彭波郑国沛贺智敏

【Author】 GU Yixue1,WANG Chengkun1,YIN Jiang2,PENG Bo2,ZHENG Guopei2,HE Zhimin1,2 (1.Cancer Research Institute,Cancer Hospital,Guangzhou Medical University,Guangzhou 510182; 2.Institute of Cancer Research,Central South University,Changsha 410078,China)

【机构】 广州医学院附属肿瘤医院肿瘤研究所中南大学肿瘤研究所

【摘要】 目的:研究新的耐药相关基因TCRP1在口腔鳞癌组织中的表达及其与顺铂临床疗效的关系,同时对TCRP1的作用机制进行初步探索。方法:采用免疫组织化学法检测TCRP1在舌癌组织中的表达及其与临床顺铂化学治疗疗效之间及体外药敏实验的相关性,Western印迹法及免疫共沉淀甄别TCRP1下游的作用分子。结果:在TCRP1低表达的患者中,缓解率达84.62%,而高表达患者组中缓解率为37.5%。体外药敏结果显示类似的结果。TCRP1表达改变影响Akt信号通路分子的表达,而且TCRP1与Akt存在物理上的相互结合。结论:TCRP1的表达影响口腔鳞癌的顺铂化学治疗疗效。TCRP1介导顺铂耐药的作用机制至少部分与TCRP1对Akt信号通路调节有关。

【Abstract】 Objective: To investigate the correlation between expression of TCRP1 gene and clinical cisplatin chemotherapy response in oral squamous cell carcinoma and to explore the functional mechanism of TCRP1 gene.Methods: Immunohistochemical methods were used to detect the expression of TCRP1 in oral squamous cell carcinoma tissues.The correlation between the expression of TCRP1 and clinical chemotherapy response or the sensitivity of tongue cancer cells to cisplatin in vitro was analyzed.Western blot and co-immunoprecipitation were used to identify the down-stream functional target of TCRP1.Results: In the group of low expressed TCRP1,the clinical cisplatin-based chemotherapy response rate was 84.62%,whereas,in the group of over-expressed TCRP1,the rate was 37.5%.The drug sensitivity assay in vitro indicated similar tendency.TCRP1 expression altered the expression pattern of Akt signal pathway molecules,and there was an interaction in physics between TCRP1 and Akt.Conclusion: TCRP1 plays a critical role in contributing to response of oral squamous cell carcinoma to cisplatin-based chemotherapy,which is involved,at least partly,in modulation of Akt pathway.

【关键词】 肿瘤口腔鳞癌TCRP1顺铂Akt
【Key words】 tumororal squamous cell carcinomaTCRP1cisplatinAkt
【基金】 国家自然科学基金(30873088);国家教育部博士点专项基金(200805330009)~~
  • 【文献出处】 国际病理科学与临床杂志 ,International Journal of Pathology and Clinical Medicine , 编辑部邮箱 ,2012年06期
  • 【分类号】R739.8
  • 【被引频次】2
  • 【下载频次】127
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