期刊文献+

中国南方食管鳞癌D5S107和D5S408杂合性丢失与微卫星不稳定性 被引量:1

Loss of Heterozygosity and Microsatellite Instability of Esophageal Squmous Cell Carcinoma in South China
暂未订购
导出
摘要 【目的】研究中国南方食管癌高发地区(潮汕地区)食管鳞癌5号染色体长臂(5q)部分微卫星标记的杂合性丢失(LOH)和微卫星不稳定(MSI),为食管鳞癌相关抑癌基因的定位提供依据。【方法】采用PCR银染技术,检测58例配对食管鳞状细胞癌标本多个微卫星标记(D5S107;SHGS31088;D5S816;D5S625和D5S408)的杂合性丢失和微卫星不稳定。【结果】SHGS31088,D5S816和D5S625杂合性丢失率和微卫星不稳定都较低;而D5S107和D5S408的杂合性丢失率分别为48.5%和34.3%,微卫星不稳定率分别为9.1%和5.7%。【结论】中国南方食管鳞癌D5S107和D5S408的杂合性丢失率较高,提示在D5S107和D5S408附近可能存在食管癌相关基因。5q区域5个微卫星标记的微卫星不稳定发生率都较低,提示微卫星不稳定在中国南方食管癌发生过程中可能不占主导地位。 [Objective] To study the loss of heterozygosity (LOH) and microsatellite instability (MSI) with some microsatellite markers on 5q of esophageal squmous cell carcinoma (ESCC) in high incidence area of South China (Chaoshan area). It will provide scientific basis for looking for the position(s) of candidate tumor suppressor gene(s) on 5q in ESCC. [Methods ] Polymerase chain reaction (PCR) based on LOH and MSI was performed in 58 primary ESCC with 5 microsatellite markers(D5S107, SHGS31088, D5S816, D5S625, and D5S408).[Resuhs]Both of the frequencies of LOH and MSI were low at SHGS31088, D5S816, and D5S625. The frequencies of LOH at D5S107 and D5S408 were 48.5% and 34.3%, respectively. The frequencies of MSI at D5S107 and D5S408 were 9.1% and 5.7%, respectively. [Conclusions]According to the high frequencies of LOH at D5S107 and D5S408, there probably existed tumor suppressor gene (s) around D5S107 and D5S408 in ESCC of South China. On the other hand, the frequencies of MSI at 5 microsatellite markers on 5q were very low, indicating MSI might not be the most important reason for the occurrence in ESCC of South China.
出处 《中山大学学报(医学科学版)》 CAS CSCD 北大核心 2008年第2期135-138,共4页 Journal of Sun Yat-Sen University:Medical Sciences
基金 国家自然科学基金(30600731) 广东省自然科学基金(04009346) 中山大学“985”二期工程基金
关键词 食管肿瘤 杂合性丢失 微卫星不稳定 D5S107 D5S408 esophageal carcinoma loss of heterozygosity microsatellite instability D5S107 D5S408
  • 相关文献

参考文献4

二级参考文献53

  • 1Zhou X,Oncogene,1994年,9卷,12期,3737页
  • 2朱丹,中华医学遗传学杂志,1994年,11卷,354页
  • 3李万波,自然科学进展,1994年,4卷,4期,461页
  • 4Huang J H,Am J Hum Genet,1990年,47卷,3期,A9页
  • 5吴--,Genetic epidemiology of cancer,1989年
  • 6Wang LD, Zheng S. The mechanism of esophageal and gastric cardia carcinogenesis from the subjects at high-incidence area for esophageal cancer in Henan. Zhengzhou Daxue Xuebao 2002; 37: 717-729.
  • 7Cullis CA. The use of DNA polymorphisms in genetic mapping. Genet Eng 2002; 24: 179-189.
  • 8Wang LD, Shi ST, Zhou Q, Goldstein S, Hong JY, Shao P, Qiu SL, Yang CS. Changes in p53 and cyclin D1 protein levels and cell proliferation in different stages of human esophageal and gastric-cardia carcinogenesis.Int J Cancer 1994; 59: 514-519.
  • 9Wang LD, Zhou Q, Hong JY, Qiu SL, Yang CS. p53 protein accumulation and gene mutations in multifocal esophageal precancerous lesions from symptom free subjects in a high incidence area for esophageal carcinoma in Henan, China. Cancer 1996; 77: 1244-1249.
  • 10Wang LD, Hong JY, Qiu SL, Gao H, Yang CS. Accumulation of p53 protein in human esophageal precancerous lesions: a possible early biomarker for carcinogenesis. Cancer Res 1993; 53: 1783-1787.

共引文献23

同被引文献10

引证文献1

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部