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消化道肿瘤淋巴结转移灶多药耐药性的变化及其意义 被引量:28

The changes of mnltidrug resistance in metastatic lymph nodes of gastrointestinal tnmors
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摘要 目的探讨消化道肿瘤淋巴结转移灶多药耐药性(MDR)的变化。方法对55例胃癌、大肠癌原发灶及相应淋巴结转移灶分别进行MDR相关蛋白(MRP)、P-糖蛋白(gp)、DNA拓扑异物酶(Topo)Ⅱα、谷胱甘肽S转移酶(GST)-л免疫组织化学染色,比较二病灶间诸指标表达程度的差异。结果原发灶与淋巴结转移灶比较:(1)两者的MRP、P-gp、TopoⅡα、GST-л表达一致率分别为32.7%、40.0%、45.5%、50.9%;(2)P-gp、GST-л阳性表达差异均有统计学意义(P<0.01); (3)中高分化腺癌的MRP、TopoⅡα阳性表达差异均有统计学意义(P<0.01,P<0.05),低分化腺癌仅GST-л阳性表达差异有统计学意义(P<0.01)。中高分化腺癌与低分化腺癌比较:原发灶中TopoⅡα阳性表达、转移灶中MRP及TopoⅡα阳性表达差异均有统计学意义(P<0.05)。结论消化道肿瘤淋巴结转移灶存在MDR的异质性变化,肿瘤原发灶的耐药基因相关蛋白表达水平不能预测淋巴结转移灶的MDR。 Objective To investigate the difference of multidrug resistance (MDR) between gastrointestinal primary tumors (PTs) and metastatic lymph nodes (MLNs). Methods The S-P immunohistochemical technique was used to detect multidrug resistance-associated protein (MRP), P-glycoprotein (P-gp) ,topoisomerase Ⅱα(TopoⅡα) and glutathione S transferase (GST-n) expression in PTs and MLNs from 48 cases of gastrointestinal tumors with metastatsis of lymph nodes. Results There was statistical difference in P-gp or GST-n expression (P 〈 0.01) between PTs and MLNs. Significant difference in MRP or Topo I] a expression was found in well differentated adenocarcinomas between PTs and MLNs (P 〈 0.01, P 〈 0.05), and GST-n expression in poorly differentated adenocarcinomas (P〈0.01 ). As compared between well and poorly differentated adenocarcinomas, the difference in the Topo Ⅱα expression level in PTs was statistically significant ( P 〈 0.05 ), and difference in MRP or TopoⅡα level expression also was significant in MLNs ( P 〈 0.05). Conclusion There was significant heterogeneity of MDR in metastatic lymph nodes as compared with gastrointestinal primary tumors. Resistance-associated proteins as MRP, P-gp,TopoⅡα, GST-n expression levels in PTs cannot be used to predict MDR of MLNs.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2006年第12期1495-1496,共2页 Chinese Journal of Experimental Surgery
基金 河北省科技攻关计划项目(05276164)
关键词 肿瘤 消化道 转移 淋巴结 多药耐药性 耐药基因相关蛋白 Tumors, gestrointestine Metastatsis, lymph nodes Multidrug resistance Multidrug resistance proteins
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