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人结肠癌染色体1q杂合性缺失分析

黄幼生 解娜 邓晓佳 宋伟伟 罗志飞

肿瘤防治研究2011,Vol.38Issue(6):658-662,5.
肿瘤防治研究2011,Vol.38Issue(6):658-662,5.DOI:10.3971/j.issn.1000-8578.2011.06.013

人结肠癌染色体1q杂合性缺失分析

Loss of Heterozygosity on Chromosome 1q in Human Colon Carcinoma

黄幼生 1解娜 1邓晓佳 1宋伟伟 1罗志飞1

作者信息

  • 1. 520101,海口,海南医学院病理教研室
  • 折叠

摘要

Abstract

Objective To define the minimally lost regions(MLR) on chromosome lq, and further to explore the molecular genetics alteration during the malignant progression of human colon mucosa. Methods Fifteen microsatellite markers were used and combined with PCR to detect the frequencies of LOH of every selected microsatellite site on chromosome 1q in colon carcinoma. Results Chromosome 1q LOH was identified in 69 of 93 colon carcinoma (74. 2%). The LOH values in the D1S413 (34. 62%) and D1S305 (43. 75) were higher than that in other microsatellite markers. Through analyzing allelic loss mapping on chromosome 1q in colon carcinoma, we found that the common lost regions are between D1S2878 ~D1S2346(1q21.3~1q23. 2) as well as D1S413~D1S249(1q31.3 ~1q32. 1). The MLR was in D1S249~D1S413, which was about 7. 1cM. A significant association was found between chromosome 1q LOH and histopathological grade, and the frequencies of LOH is the highest in poor differentiated colon carcinoma (P<0. 05). Conclusion There are high LOH frequency on the chromosome 1q31.3 ~1q32. 1 and 1q21.3~1q23. 2 in colon carcinoma. The result suggests these regions perhaps harbor putative tumor suppressor gene(s) contributing to tumorigenesis and differentiation in human colon carcinoma. The high frequency allelic loss on 1q is associated with colon carcinoma cell differentiation.

关键词

结肠癌/染色体1q/杂合性缺失/微卫星

Key words

Colon cancer/ Loss of heterozygosity/ Chromosome 1q/ Microsatellite markers

分类

医药卫生

引用本文复制引用

黄幼生,解娜,邓晓佳,宋伟伟,罗志飞..人结肠癌染色体1q杂合性缺失分析 [J].肿瘤防治研究,2011,38(6):658-662,5.

基金项目

海南省教育厅基金资助项目(2007047) (2007047)

肿瘤防治研究

OA北大核心CSCDCSTPCD

1000-8578

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