期刊文献+

消化道肿瘤淋巴结转移灶P-糖蛋白、谷胱甘肽S转移酶-π和凋亡抑制蛋白的表达特点 被引量:14

Expression features of P-glycoprotein, glutathione S transferase-π and inhibitor of apoptosis proteins in lymph node metastases of gastrointestinal carcinomas
原文传递
导出
摘要 目的探讨消化道肿瘤淋巴结转移灶多药耐药相关因子P-糖蛋白(P—gp)、谷胱甘肽S转移酶-π(GST-π)、p53、survivin、bcl-2的表达特点及临床意义。方法对54例胃癌和大肠癌的转移淋巴结、原发灶中上述5种多药耐药相关因子行免疫组织化学染色,对比其表达的差异。结果转移灶与原发灶相比,P-gp、GST-π在二者问表达的差异具有统计学意义(P均〈0.05);p53、bcl-2表达在二者之间具有明显相关性(r=0.7248、0.5524;P均〈0.05)。在转移淋巴结,P—gp分别与GST-π及survivin表达呈正相关(r=0.4062、0.6169,P均〈0.05),CST-πT与survivin表达呈正相关(r=0.4027,P〈0.05);而在原发灶,bcl-2与P—gp及survivin表达呈正相关(r=0.3986、0.2937,P均〈0.05)、GST-π与survivin表达呈正相关(r=0.4481,P〈0.01),仅GST-π与survivin正相关表达同时出现在转移灶和原发灶内。结论消化道肿瘤淋巴结转移灶存在多药耐药相关因子表达的异质性,肿瘤切除术后辅助化疗的靶目标应针对淋巴结转移灶。 Objective To investigate the expression features of P-glycoprotein (P-gp), glutathione S transferase-π (GST-π) and inhibitor of apoptosis proteins like p53, survivin and bcl-2 in lymph node metastases of gastrointestinal carcinomas. Methods The expression of P-gp, GST-π, p53, survivin and bcl- 2 were determined by using immunohistochemistrical technique in surgical specimens of primary tumor (PT) and lymph node metastases (LNMs) from 54 gastrointestinal cancer patients with metastatsis of lymph nodes. The expression difference of 5 muhidrugs resistance (MDR)-related factors between LNMs and PT were compared. Results Significant difference was found in the expression of P-gp and GST-π between the two groups ( both P 〈 0. 05 ) , and expression of p53 and bcl-2 showed positive correlation between LNMs and PT ( r = 0. 7248, 0. 5524 ; both P 〈 0. 05 ), respectively. In LNMs, P-gp expression was positively correlated with GST-π ( r = 0. 4062, P 〈 0. 05 ) and survivin ( r = 0. 6169, P 〈 0. 05 ), and also GST-π expression was related positively with survivin ( r = 0. 4027, P 〈 0. 05 ). Statistically positive correlations were noted between bel-2 and P-gp ( r = 0. 3986, P 〈 0. 05 ), bel-2 and survivin ( r = 0. 2937, P 〈 0. 05) , as well as GST-π and survivin ( r = 0. 4481, P 〈 0. 01 ) in PT. Only a positive correlation between GST-π and survivin expression was simultaneously shown in both LNMs and FT. Conclusions There is significant heterogeneity of MDR-related factors expression in LNMs of gastrointestinal carcinomas. Effective adjuvant chemotherapy after operation should target on the metastatic loci of the disease.
出处 《中华外科杂志》 CAS CSCD 北大核心 2009年第2期106-108,共3页 Chinese Journal of Surgery
基金 河北省科技计划基金资助项目(06276102D-73)
关键词 消化道肿瘤 淋巴结转移 多药耐药性 P-糖蛋白 谷胱甘肽S-转移酶-Π Gastrointestinal carcinomas Muhidrugs resistance Lymph node metastases P-glycoprotein Glutathione S transferase-π
  • 相关文献

参考文献4

二级参考文献34

  • 1李海,郑春宁,薛强,万厚民,王震宇.胃癌组织中的肺耐药蛋白、P糖蛋白、谷胱甘肽-S-转移酶以及拓扑异构酶Ⅱ的表达及意义[J].中华实验外科杂志,2005,22(1):58-59. 被引量:17
  • 2Miyoshi Y,Ando A,Takamura Y,et al . Prediction of response to docetaxel by CYP3A4 mRNA expression in breast cancer tissues. Int J Cancer,2002,97 ( 1 ) : 129-132.
  • 3Tucker AN,Tkaczuk KA, Lewis LM, et al . Polymorphisms in cytochrome P4503A5 (CYP3A5) may be associated with race and tumor characteristics, but not metabolism and side effects of tamoxifen in breast cancer patients. Cancer Lett,2005,217( 1 ) :61-72.
  • 4Michael M, Doherty MM. Tumoral Drug Metabolism : Overview and Its Implications for Cancer Therapy, J Clin Oncol, 2005,23 ( 1 ) : 205-229.
  • 5Townsend DM ,Tew KD. The role of glutathione-S-transferase in anticancer drug resistance. Oncogene,2003,22(47) :7369-7375.
  • 6Davis RJ. Signal transduction by the JNK group of MAP kinases.Cell,2000,103 (2) :239-252.
  • 7Fan M, Chambers TC . Role of mitogen-activated protein kinases in the response of tumor cells to chemotherapy. Drug Resist Updat,2001,4(4) :253-267.
  • 8Synold TW, Dussault I, Forman BM . The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux. Nat Med,2001,7(5) :584-590.
  • 9Takami N, Sakamoto H, Yamamoto T. Steroid and xenobiotic receptor(SXR) is a key system for the acquisition of cisplatin resistance in endometrial cancer cells. J Int Med Res,2003,31 (2) :59-68.
  • 10Doyle LA, Ross DD . Multidrug resistance mediated by the breast cancer resistance protein BCRP ( ABCG2 ). Oncogene, 2003, 22(47) :7340-7358.

共引文献59

同被引文献124

引证文献14

二级引证文献32

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部