华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

肿瘤耐药蛋白在舌鳞癌中的表达及意义

冷卫东,王大章,冯戈,何嘉   

  1. 四川大学教育部口腔生物医学工程教育部重点实验室,四川 成都610041
  • 收稿日期:2004-02-25 修回日期:2004-02-25 出版日期:2004-02-20 发布日期:2004-02-20
  • 通讯作者: 冷卫东,Tel:13684079810
  • 作者简介:冷卫东(1968-),男,湖北人,主治医师,博士
  • 基金资助:

    国家自然科学基金资助项目(39970798);四川大学优秀博士论文研究基金资助项目(0040305505010)

Expression and Implication of Pgp, MRP, LRP, GST-π, TopoⅡαin Tongue Squamous Cell Carcinoma

LENG Wei- dong,WANG Da-zhang,FENG Ge,HEJia   

  1. KeyLab.ofOral Biomedical Engineering,Ministry ofEducation,Sichuan Uni- versity,Chengdu610041,China
  • Received:2004-02-25 Revised:2004-02-25 Online:2004-02-20 Published:2004-02-20

摘要:

目的 检测P-糖蛋白(Pgp),多药耐药相关蛋白(MRP),肺耐药相关蛋白(LRP),谷胱苷肽-S转移酶(GST-π) 及DNA拓扑异构酶Ⅱα(TopoⅡα)在舌鳞癌组织中的表达水平及与化疗疗效的关系。方法 采用卡铂、平阳霉素和氨甲喋呤化疗方案对40例舌鳞癌患者进行化疗,分别于化疗前和化疗后用免疫组织化学LsAB法检测Pgp,MRP, LRP,GST-π,TopoⅡα在80例舌鳞癌组织中的表达,其中40例为化疗前,40例为化疗后。结果 在检测的舌癌组织中,化疗前Pgp,MRP,LRP,GST-π,TopoⅡα的阳性表达率分别为47·5%,50%,35%,45%,82·5%,它们的表达与临床病理无关(P>0·05);Pgp,MRP化疗前后水平上升(P<0·05);Pgp,MRP与化疗耐药效果有关(P<0·05);共表达现象普遍,Pgp,MRP,GST-π及MRP,GST-π联合表达率在化疗无效者中为40%和50%,而在化疗有效者中为0。结论 Pgp,MRP,GST-π的共表达与舌鳞癌的原发性耐药有关。

关键词: 舌鳞癌, 多药耐药, P-糖蛋白, 多药耐药相关蛋白, 谷胱苷肽-S转移酶

Abstract:

Objective To explore the correlation of chemotherapy efficacy in tongue squamous cell carcinoma(SCC) with ex- pression level of P-glycoprotein(Pgp), multidrug resistance-associated protein (MRP), lung resistance-related protein (LRP), glutathiones-tranferase (GST-π), DNAtopo-isomeraseⅡα(TopoⅡα).Methods The expression patterns of Pgp, MRP, LRP, GST-πand TopoⅡαin 40 patients (pre and post-chemotherapy, respectively) with tongue SCC were examined by immunohisto- chemically labelled streptavidin bioein method (LsAB).Results The expression ratios of Pgp, MRP, LRP, GST-πand TopoⅡ αin pre-chemotherapy cases were 47·5%, 50%, 35%, 45%, 82·5%, respectively. No relations between expression of Pgp, MRP, LRP, GST-π, TopoⅡαand clinic indexes were established (P>0·05). Expression ratios of Pgp, MRP in post-chemo- therapy cases were higher than that in pre-chemotherapy cases (P<0·05). Expression of Pgp and MRP showed relevance with drug resistance (P<0·05). The co-expressionwas common, the ratios of co-expression of Pgp, MRP, GST-πandMRP, GST-π in chemotherapy non-responders were 40% and 50%, respectively, but 0 in responders.Conclusion The intrinsic multidrug resistance of tongue SCC is relevant to the effects of Pgp, MRP, GST-π.

Key words: tongue sequamous cell carcinoma, multidrug resistance, P-glycoprotein, multidrug resistance-associated protein, glutathione-S-tranferase