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胞内氯离子通道蛋白1表达与胆囊癌侵袭转移的相关性研究 被引量:1

CLIC1 protein expression correlates with invasion and metastasis of gallbladder cancer
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摘要 目的探讨胆囊癌组织胞内氯离子通道蛋白1(chloride intraeellular channel 1,CLICl)蛋白表达与胆囊癌侵袭转移的关系。方法应用免疫组织化学sP染色法及Westernblot技术,检测36例胆囊癌和相应癌旁组织中CLICl蛋白的表达。采用Spearman等级相关分析、x。检验对结果进行分析。结果免疫组化结果提示,CLICl蛋白高表达于胆囊癌组织,癌旁组织中CLICl蛋白表达较少,阳性表达率分别为81%(29/36)和44%(16/36),差异有统计学意义(P〈0.05)。胆囊癌组织CLICl表达与患者性别和年龄无关(P〉0.05),而与肿瘤的淋巴转移、浸润深度、TNM分期和分化程度相关(P〈0.05)。Westernblot结果显示,CLICl的特异性条带出现在Marker标准相对分子质量27000左右,CLICl在胆囊癌的阳性率高于癌旁组织(P〈0.05)。结论CLICl可能在胆囊癌的发生发展过程中发挥重要的作用,CLICl蛋白的高表达与胆囊癌的侵袭转移密切相关。 Objective To investigate the correlation between the CLIC1 protein expression with the invasion and metastasis in gallbladder cancer. Methods The expressions of CLIC1 was detected in 36 matching-samples including primary gallbladder cancer tissues and paratumor normal tissues by immunohistochemistry and Western blot. All data were analyzed via Spearman rank correlation coefficient and chi-square test. Results The over-expression of CLIC1 was found in 81% (29/36)of the gallbladder cancer tissues, whereas in 44% (16/36) of paratumor normal tissues. There were significant differences in the expression of CLIC1 between them (P 〈0. 05). The expression of CLIC1 did not correlate with age and sex of patients(P 〉 0. 05 ), but with tumor differentiation and lymph node metastasis (P 〈 0.05 ). Western blot displayed clear bands of CLIC1 about 27 000 by molecular weight marker Mix, and there was a significant difference between the high expressions of CLIC1 in gallbladder cancer and the low expressions in paratumor normal tissues(P 〈 0.05). Conclusions CLIC1 may play an important role in tumorigenesis of gallbladder cancer. The invasion and metastasis of gallbladder cancer lesions are correlated with the expression of CLIC1.
出处 《中华普通外科杂志》 CSCD 北大核心 2013年第2期112-115,共4页 Chinese Journal of General Surgery
基金 教育部博士点基金(博导类)资助项目(2011(137311(1386) 国家自然科学基金面上资助项目(30972918、81172029、81172026)
关键词 胆囊肿瘤 肿瘤侵润 细胞凋亡 胞内氯离子通道蛋白1 Gallbladder neoplasms Neoplasm invasiveness Apoptosis Chloride intracellularchannel 1
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