Gastric Cancer Pathology and Underlying Molecular Mechanisms

被引:76
作者
Grabsch, Heike I. [1 ,2 ]
Tan, Patrick [3 ,4 ,5 ,6 ]
机构
[1] Univ Leeds, Leeds Inst Canc & Pathol, Leeds LS9 7TF, W Yorkshire, England
[2] Leeds Teaching Hosp NHS Trust, St Jamess Inst Oncol, Dept Histopathol & Mol Pathol, Leeds, W Yorkshire, England
[3] Natl Univ Singapore, Duke NUS Grad Med Sch, Singapore 117548, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Canc Sci Inst Singapore, Singapore 117595, Singapore
[5] Genome Inst Singapore, Singapore, Singapore
[6] Natl Canc Ctr, Singapore, Singapore
关键词
Gastric cancer; Genetic alterations; Pathology; COMPARATIVE-GENOMIC-HYBRIDIZATION; EXPRESSION MICROARRAY ANALYSIS; HMLH1 GENE PROMOTER; MICROSATELLITE INSTABILITY; COPY NUMBER; CLINICOPATHOLOGICAL FEATURES; INTESTINAL METAPLASIA; PRECANCEROUS LESIONS; HISTOLOGICAL TYPE; PROGNOSTIC-FACTOR;
D O I
10.1159/000350876
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The development of gastric adenocarcinoma is a complex multistep process involving multiple genetic alterations. Based on pathology, four different macroscopic types and at least two major histological types, intestinal and diffuse, have been described. Most gastric cancer (GC) show genetic instability, either microsatellite instability or chromosomal instability, which is considered an early event in gastric carcinogenesis. Molecular studies of alterations of single genes have provided evidence that intestinal and diffuse type GC evolve via different genetic pathways. Recent results from high-throughput whole-genome expression or copy number studies have demonstrated extensive genetic diversity between cases and within individual GC. Sets of commonly up-or downregulated microRNAs have been identified in GC and might be useful in the near future to identify pathways of GC progression. Results from detailed molecular and/or pathological GC studies, although promising, still have limited clinical utility in predicting survival and stratifying GC patients for appropriate treatment. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:150 / 158
页数:9
相关论文
共 102 条
[1]  
[Anonymous], 2003, GASTROINTEST ENDOSC, V58, pS3
[2]  
[Anonymous], 2010, WHO CLASSIFICATION T
[3]  
Bang YJ, 2010, LANCET, V376, P1302
[4]   Gross genomic damage measured by DNA image cytometry independently predicts gastric cancer patient survival [J].
Belien, J. A. M. ;
Buffart, T. E. ;
Gill, A. J. ;
Broeckaert, M. A. M. ;
Quirke, P. ;
Meijer, G. A. ;
Grabsch, H. I. .
BRITISH JOURNAL OF CANCER, 2009, 101 (06) :1011-1018
[5]  
Borrmann R, 1926, HDB SPEZIELLEN PATHO, P864
[6]   Gastric cancers in young and elderly patients show different genomic profiles [J].
Buffart, T. E. ;
Carvalho, B. ;
Hopmans, E. ;
Brehm, V. ;
Kranenbarg, E. Klein ;
Schaaiji-Visser, T. B. M. ;
Eijk, P. P. ;
van Grieken, N. C. T. ;
Ylstra, B. ;
van de Velde, C. J. H. ;
Meijer, G. A. .
JOURNAL OF PATHOLOGY, 2007, 211 (01) :45-51
[7]   Gastric cancers of Western European and African patients show different patterns of genomic instability [J].
Buffart, Tineke E. ;
Louw, Melanie ;
van Grieken, Nicole C. T. ;
Tijssen, Marianne ;
Carvalho, Beatriz ;
Ylstra, Bauke ;
Grabsch, Heike ;
Mulder, Chris J. J. ;
van de Velde, Cornelis J. H. ;
van der Merwe, Schalk W. ;
Meijer, Gerrit A. .
BMC MEDICAL GENOMICS, 2011, 4
[8]   High resolution analysis of DNA copy-number aberrations of chromosomes 8, 13, and 20 in gastric cancers [J].
Buffart, Tineke E. ;
van Grieken, Nicole C. T. ;
Tijssen, Marianne ;
Coffa, Jordy ;
Ylstra, Bauke ;
Grabsch, Heike I. ;
van de Velde, Cornelis J. H. ;
Carvalho, Beatriz ;
Meijer, Gerrit A. .
VIRCHOWS ARCHIV, 2009, 455 (03) :213-223
[9]   DNA copy number profiles of gastric cancer precursor lesions [J].
Buffart, Tineke E. ;
Carvalho, Beatriz ;
Mons, Thomas ;
Reis, Rui M. ;
Moutinho, Catia ;
Silva, Paula ;
van Grieken, Nicole C. T. ;
Vieth, Michael ;
Stolte, Manfred ;
van de Velde, Cornelis J. H. ;
Schrock, Evelin ;
Matthaei, Anja ;
Ylstra, Bauke ;
Carneiro, Fatima ;
Meijer, Gerrit A. .
BMC GENOMICS, 2007, 8
[10]  
C F., 1997, Curr Diag Pathol, V4, P51