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K-ras基因突变与结直肠癌生物学行为的关系

吴文辉 肖隆斌 汤友珍 蔡世荣 詹文华

中国病理生理杂志2009,Vol.25Issue(11):2159-2162,4.
中国病理生理杂志2009,Vol.25Issue(11):2159-2162,4.

K-ras基因突变与结直肠癌生物学行为的关系

Relationship between mutated k - ras and biological behavior of colorectal cancer

吴文辉 1肖隆斌 1汤友珍 1蔡世荣 2詹文华2

作者信息

  • 1. 中山大学附属第一医院黄埔院区普外科,广东,广州,510700
  • 2. 中山大学附属第一医院胃肠胰外科,广东,广州,510080
  • 折叠

摘要

Abstract

AIM: To investigate mutations of oncogene k-ras in colorectal cancer tissues and the relationship between mutations of k - ras and biological behavior of colorectal carcinoma. METHODS:The specimens of 123 patients with colorectal cancer were collected. Real - time fluorescence quantitative PCR were performed to detect k-ras mutations at codon 12 and codon 13 of exon 1, and the results were analyzed with the corresponding clinical pathological data. RESULTS: Among 123 colorectal cancer cases, point mutations were detected in 53 cases (40.8% ) , point mutations at codon 12 were found in 42 (34.1 % ) cases, and 11(8.9% ) cases at codon 13.No closely relationship between mutations of k-ras and tumor size, location, invasive depth and differentiation extent was observed. The rate of k-ras mutation in the cases with more invaded lymph nodes was higher than that in the cases without invaded lymph nodes ( P < 0.05 ) , and the rate of k-ras gene mutation in the cases with hepatic metastases was higher than that in no hepatic metastases (P <0.05). The rate of k - ras gene mutation was higher in TNM staging Ⅲ/Ⅳ than that in Ⅰ/Ⅱ( P < 0.05 ). CONCLUSION: Mutation of oncogene k-ras plays an important role in the carcinogenesis and development of colorectal cancer, and it is closely associated with invaded lymph notes and hepatic metastases, suggesting that mutation of k- ras indicates a poor prognosis.

关键词

结直肠肿瘤/基因/突变/肿瘤转移

Key words

Colorectal neoplasms/ Genes/ Mutation/ Neoplasm metastasis

分类

医药卫生

引用本文复制引用

吴文辉,肖隆斌,汤友珍,蔡世荣,詹文华..K-ras基因突变与结直肠癌生物学行为的关系[J].中国病理生理杂志,2009,25(11):2159-2162,4.

基金项目

广州市黄埔区科技计划资助项目(No.2009031) (No.2009031)

中国病理生理杂志

OA北大核心CSCDCSTPCD

1000-4718

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