Barrett's oesophagus: an ideal model to study cancer genetics

被引:12
作者
di Pietro, Massimiliano [1 ]
Fitzgerald, Rebecca C. [1 ]
机构
[1] Hutchison MRC Res Ctr, Canc Cell Unit, Cambridge CB2 0XZ, England
基金
英国医学研究理事会;
关键词
GASTROESOPHAGEAL-REFLUX DISEASE; HIGH-GRADE DYSPLASIA; NITRIC-OXIDE SYNTHASE; DNA-REPAIR GENES; FACTOR-KAPPA-B; BILE-ACIDS; MOLECULAR PATHOGENESIS; NEOPLASTIC PROGRESSION; INTESTINAL METAPLASIA; SQUAMOUS EPITHELIUM;
D O I
10.1007/s00439-009-0665-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chronic gastro-oesophageal reflux disease can induce a metaplastic change of the distal oesophagus called Barrett's oesophagus whereby the normal squamous epithelium is substituted by a columnar epithelium. Patients with Barrett's oesophagus are at increased risk of oesophageal adenocarcinoma which occurs through dysplastic stages with increasing degree of cellular and architectural disorganization. Barrett's oesophagus represents an ideal model to study the genetic events supporting the onset of an invasive tumour since patients with this condition are surveilled with endoscopic tissue sampling until high grade dysplasia or intramucosal carcinoma develop. However, due to the relatively low incidence of this disease compared to other cancers, i.e. colon and breast, it is only recently that researchers have concentrated on understanding the genetic events supporting the onset of Barrett's and its transformation to cancer. Here, we review the knowledge acquired so far on the genetic and molecular alterations along the oesophageal metaplasia-dysplasia-carcinoma sequence.
引用
收藏
页码:233 / 246
页数:14
相关论文
共 183 条
[11]   Obesity prevalence from a European perspective:: a systematic review [J].
Berghoefer, Anne ;
Pischon, Tobias ;
Reinhold, Thomas ;
Apovian, Caroline M. ;
Sharma, Arya M. ;
Willich, Stefan N. .
BMC PUBLIC HEALTH, 2008, 8 (1)
[12]   Chromosomal numerical aberrations are frequent in oesophageal and gastric adenocarcinomas:: a study using in-situ hybridization [J].
Beuzen, F ;
Dubois, S ;
Fléjou, JF .
HISTOPATHOLOGY, 2000, 37 (03) :241-249
[13]   CLONAL ORDERING OF 17P AND 5Q ALLELIC LOSSES IN BARRETT DYSPLASIA AND ADENOCARCINOMA [J].
BLOUNT, PL ;
MELTZER, SJ ;
YIN, J ;
HUANG, Y ;
KRASNA, MJ ;
REID, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3221-3225
[14]   Cytostatic drug treatment causes seeding of gene promoter methylation [J].
Bredberg, Anders ;
Bodmer, Walter .
EUROPEAN JOURNAL OF CANCER, 2007, 43 (05) :947-954
[15]   Incidence of adenocarcinoma of the esophagus among white Americans by sex, stage, and age [J].
Brown, Linda Morris ;
Devesa, Susan S. ;
Chow, Wong-Ho .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (16) :1184-1187
[16]   Extent of high-grade dysplasia in Barrett's esophagus correlates with risk of adenocarcinoma [J].
Buttar, NS ;
Wang, KK ;
Sebo, TJ ;
Riehle, DM ;
Krishnadath, KK ;
Lutzke, LS ;
Anderson, MA ;
Petterson, TM ;
Burgart, LJ .
GASTROENTEROLOGY, 2001, 120 (07) :1630-1639
[17]   Chemoprevention of esophageal adenocarcinoma by COX-2 inhibitors in an animal model of Barrett's esophagus [J].
Buttar, NS ;
Wang, KK ;
Leontovich, O ;
Westcott, JY ;
Pacifico, RJ ;
Anderson, MA ;
Krishnadath, KK ;
Lutzke, LS ;
Burgart, LJ .
GASTROENTEROLOGY, 2002, 122 (04) :1101-1112
[18]   Gastroesophageal reflux disease in monozygotic and dizygotic twins [J].
Cameron, AJ ;
Lagergren, J ;
Henriksson, C ;
Nyren, O ;
Locke, GR ;
Pedersen, NL .
GASTROENTEROLOGY, 2002, 122 (01) :55-59
[19]   Cyclin D1 polymorphism (G870A) and risk for esophageal adenocarcinoma [J].
Casson, AG ;
Zheng, ZY ;
Evans, SC ;
Geldenhuys, L ;
van Zanten, SV ;
Veugelers, PJ ;
Porter, GA ;
Guernsey, DL .
CANCER, 2005, 104 (04) :730-739
[20]   Polymorphisms in DNA repair genes in the molecular pathogenesis of esophageal (Barrett) adenocarcinoma [J].
Casson, AG ;
Zheng, ZY ;
Evans, SC ;
Veugelers, PJ ;
Porter, GA ;
Guernsey, DL .
CARCINOGENESIS, 2005, 26 (09) :1536-1541