首都医科大学学报 ›› 2012, Vol. 33 ›› Issue (2): 223-226.doi: 10.3969/j.issn.1006-7795.2012.02.018

• 基础研究 • 上一篇    下一篇

c-Met在食管鳞状细胞癌组织中的表达及其与临床病理的相关性

刘春涛, 朱圣韬, 田月, 张澍田   

  1. 首都医科大学附属北京友谊医院消化内科 北京市消化疾病中心,北京 100050
  • 收稿日期:2011-11-17 修回日期:1900-01-01 出版日期:2012-04-21 发布日期:2012-04-21
  • 通讯作者: 张澍田

c-Met expression in esophageal squamous cell carcinoma tissues and its correlation with clinicopathological characteristics

LIU Chun-tao, ZHU Sheng-tao, TIAN Yue, ZHANG Shu-tian   

  1. Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing Digestive Disease Center, Beijing 100050, China
  • Received:2011-11-17 Revised:1900-01-01 Online:2012-04-21 Published:2012-04-21

摘要: 目的 检测食管鳞状细胞癌组织及配对癌旁组织中c-Met蛋白的表达情况,探讨c-Met的表达与食管鳞状细胞癌患者临床病理特点的相关性。方法 收集87对甲醛固定,石蜡包埋的食管鳞状细胞癌及配对的癌旁组织标本,所有病例均经病理证实,同时收集患者的临床资料。采用免疫组化的方法检测组织中c-Met的表达情况。结果 c-Met主要表达于细胞膜,表现为胞膜呈棕黄色染色。87例食管鳞癌组织中有29例(33.3%)呈阳性表达。配对癌旁组织中未见c-Met表达。c-Met的表达与食管鳞状细胞癌患者的肿瘤浸润深度、淋巴结转移及临床病理分期(tumor-node-metastasis,TNM)存在显著相关性(分别为P=0.017,P=0.000,P=0.000),而与患者的性别、年龄、肿瘤细胞分化程度、肿瘤大小等无明显相关性(P>0.05)。结论 c-Met在部分食管鳞癌组织中呈高表达,且与患者的肿瘤浸润深度、淋巴结转移及TNM分期存在显著相关性,c-Met的高表达可以作为高侵袭性食管鳞癌的分子标志物。

关键词: 食管鳞状细胞癌, c-Met, 肝细胞生长因子, 临床病理

Abstract: Objective To detect the expression of c-Met in esophageal squamous cell carcinoma tissues(ESCC) and paired non-cancerous tissues, and to investigate the association between c-Met and clinicopathological parameters of ESCC patients. Methods Eighty seven pairs of paraffin-embedded ESCC tissues and paired non-cancerous esophageal tissues were collected from the Department of Pathology, Beijing Friendship Hospital Affiliated To Capital Medical University. Sections from each specimen were examined by a pathologist and graded histologically. Patients' clinical parameters were collected meanwhile. Immunohistochemistry(IHC) was applied to detected the the expression of c-Met in the tissues. Results c-Met positive signals showed brown-yellow granules in the membrane. The expression of c-Met in non-cancerous esophageal tissues was always negative, whereas strong positive staining of c-Met was observed in 29/87(33.3%) of ESCCs. The expression of c-Met was correlated with tumor invasion depth, lymph node metastasis, and TNM(tumor-node-metastasis) stage(P=0.017, P=0.000, P=0.000, respectively). No significant association between c-Met expression and other clinicopathological parameters(patients' gender, age, cell grading, and tumor size) was found(P>0.05). Conclusion The overexpression of c-Met was correlated with tumor invasion depth, lymph node metastasis, and TNM stage of ESCC patients. The overexpression of c-Met may be a marker for highly invasive ESCC.

Key words: esophageal squamous cell carcinoma, c-Met, hepatocyte growth factor, clinicopathology

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