Abstract
王立东,刘宾,郑树.林州居民食管癌p53基因突变谱分析与不同地区食管癌和其他类型肿瘤的比较[J].Chinese journal of Epidemiology,2003,24(3):202-205
林州居民食管癌p53基因突变谱分析与不同地区食管癌和其他类型肿瘤的比较
Analysis of p53 mutational spectra of esophageal squamous cell carcinomas from Linzhou, comparison with esophageal and other cancers from other areas
Received:March 20, 2002  
DOI:
KeyWord: p53突变谱  食管肿瘤  生物信息学
English Key Word: p53 mutation spectrum  Esophageal neoplasms  Bioinformatics
FundProject:国家杰出青年科学基金资助项目(30025016);河南省高校创新人才工程基金资助项目
Author NameAffiliation
WANG Lidong Cancer Institute, College of Medicine, Zhejiang University, Hangzhou 310009, China 
LIU Bin 首都医科大学同仁医院 
ZHENG Shu Cancer Institute, College of Medicine, Zhejiang University, Hangzhou 310009, China 
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Abstract:
      目的分析河南省林州市与其他地区食管癌前病变和鳞状细胞癌p53突变谱,探讨食管癌变的发病因素。方法采用生物信息学和MonteCarlo方法,依据IARCp53突变数据库、Curic研究院p53突变数据库和郑州大学医学院癌症研究所实验室的资料,用FileMarkPro3.0软件系统建立局部资料库进行分析。结果林州食管癌高发区食管鳞癌碱基替换的发生率低于其他地区食管鳞癌的发生率(32.8%vs39.8%),但CpG位点G∶C→A∶T的发生率高于其他地区食管癌(29.6%vs16.4%)。林州食管癌突变位点具有明显的特征,主要发生在273(占所有错义突变的11.3%)、175(9.7%)、159(6.5%)和282(6.5%)位密码子的CpG位点上。林州地区食管鳞癌p53突变与其他地区食管鳞癌以及头颈部鳞癌p53突变相比,差异有显著性(P=0.02)。结论林州食管癌p53突变具有内、外源致癌原所致突变的特征,提示慢性炎症、饮食习惯和接触致癌原,可能是林州居民发生食管鳞癌的主要危险因素
English Abstract:
      Objective To study the etiological clues involved (in esophageal cancer in Linzhou, Henan, a high-incidence area for esophageal cancer) by analyzing p53 mutational spectrum from esophageal precancerous and cancerous lesions.Methods Using bolt bioinformatic and Monte Carlo methods to analyze p53 mutation spectra from "The IARC Database of Somatic p53 Mutations in Human Tumors and Cell Lines", "p53 Database at Institute Curic" and to establish a local database based on these data using the FileMark Pro 3.0 software to allow fast and off-line analysis on a PC from the authors' laboratory. Results We found that esophageal squamous cell carcinomas from Linzhou had a lower prevalence of base substitutions associated with strand bias than those from other areas ( 32.8% vs 39.8%). However, a higher prevalence of G∶ C→ A∶T transitions at CpG site ( 29.6% vs 16.4%) was found. Esophageal squamous cell carcinomas from Linzhou displayed a distinctive profile of mutation hotspots, including codons 273 (covers 11.3% of all missense mutations), 175 ( 9.7%),158 ( 9.7%), 159 ( 6.5%) and 282 ( 6.5%), all of which were at the CpG site. Statistical analysis showed that the p53 mutation profiles between esophageal squamous cell carcinomas from Linzhou and those from other areas were different ( P= 0.02). The p53 mutation profiles of esophageal squamous cell carcinomas from Linzhou and from other areas were also different from cancer of the head and neck.Conclusion Data showed that the p53 mutational spectrum of esophageal squamous cell carcinomas from Linzhou baring the characteristics of those caused both by endogenous and exogenous mutagenic agents, suggesting the potential involvement of chronic inflammation, unique dietary habits and carcinogen exposure in the pathogenesis of esophageal squamous cell carcinoma in Linzhou.
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