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TIMP-3基因甲基化与结直肠癌临床病理的关系
引用本文:黄美近,汪建平,褚忠华,宋新明,王磊,杨祖立,蔡世荣.TIMP-3基因甲基化与结直肠癌临床病理的关系[J].中国病理生理杂志,2005,21(12):2418-2421.
作者姓名:黄美近  汪建平  褚忠华  宋新明  王磊  杨祖立  蔡世荣
作者单位:1中山大学附属第一医院胃肠胰外科, 广东 广州 510080;2中山大学附属第二医院胃肠外科, 广东 广州 510120
基金项目:教育部博土点基金资助项目(NO.20020558050)
摘    要:目的:探讨TIMP-3基因甲基化与结直肠癌临床病理指标和转移复发的关系。 方法: 采用巢式甲基化特异性PCR技术(nMSP法)检测100例结直肠癌组织和100例癌旁非癌组织TIMP-3基因甲基化;采用RT-PCR检测100例结直肠癌组织和100例癌旁非癌组织TIMP-3 mRNA的表达。 结果: 肿瘤组织TIMP-3 mRNA的表达阳性率为64%,肿瘤组织TIMP-3 mRNA的表达率明显低于癌旁非癌组织(P<0.01);TIMP-3 mRNA的表达率无淋巴结转移组(34/42)高于淋巴结转移组(30/58)(P<0.01),甲基化阳性率Duke’s C+D期伴淋巴结转移组明显高于Duke’s A+B期不伴淋巴结转移组(P<0.05)。结肠近端、分化程度差的结直肠癌组织甲基化阳性率明显高于远端直肠和分化程度高者(P<0.05)。 结论: TIMP-3基因甲基化容易发生在结肠近端、Duke’s C、D期、伴淋巴结转移、细胞分化差和浸润型结直肠癌患者。

关 键 词:结直肠肿瘤  金属蛋白酶3组织抑制剂  
文章编号:1000-4718(2005)12-2418-04
收稿时间:2005-09-01
修稿时间:2005-09-012005-11-28

Methylation of TIMP-3 gene and their relationships with their clinical-pathological characteristics of colorectal cancers
HUANG Mei-jin,WANG Jian-ping,CHU Zhong-hua,SONG Xin-ming,WANG Lei,YANG Zu-li,CAI Shi-rong.Methylation of TIMP-3 gene and their relationships with their clinical-pathological characteristics of colorectal cancers[J].Chinese Journal of Pathophysiology,2005,21(12):2418-2421.
Authors:HUANG Mei-jin  WANG Jian-ping  CHU Zhong-hua  SONG Xin-ming  WANG Lei  YANG Zu-li  CAI Shi-rong
Institution:1Department of Gastrointestinal-Pancreatic Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China;2Department of Gastrointestinal Surgery, The Second Affiliated Hospital, Sun Yat-sen University, Guangzhou 510120, China
Abstract:AIM: To investigate whether methylation of the TIMP - 3 gene is associated with clinical - pathological characteristics, recurrence and metastasis of the colorectal cancer. METHODS: Nest methylation specific PCR (nMSP) and RTPCR techniques were used to detect methylation of TTMP-3 gene and its mRNA expression in the colorectal cancer specimen and adjacent non - cancerous tissues. RESULTS: The expression of TIMP - 3 mRNA in tumor tissues was distinctly reduced (P< 0.01). The expression of TIMP - 3 mRNA in those without lymph node metastasis was higher than those with lymph node metastasis ( P<0.01). The patients with Duke's C, I) and lymph node metastasis were more to contain methylated TIMP - 3 compared to those with Duke's A, B and no lymph node metastasis (P<0.05) . Statistical differences in pathological characteristics such as tumor site, Duke' s stage, histological differentiation and type between TIMP - 3 methylation positive group and negative group were observed (P<0.05). CONCLUSION: Methylation of the TIMP - 3 gene promoter usually occurs in the proximal site, infiltrating type, poor cellular differentiation, lymph node metastasis and advanced stage of colorectal cancers patients.
Keywords:Colorectal neoplasms  Tissue inhibitor of metalloproteinase - 3  Methylation  mRNA expression
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