Editorial
Copyright ©2010 Baishideng.
World J Gastrointest Oncol. Feb 15, 2010; 2(2): 59-64
Published online Feb 15, 2010. doi: 10.4251/wjgo.v2.i2.59
Table 2 Clinico-pathological and molecular-genetic differences between early-onset and conventional gastric cancers
Conventional gastric cancerEarly-onset gastric cancerRef.
Equally common in male and femalesMore common in females[13,28,30,31]
Intestinal type cancer more commonDiffuse type cancer more common[13,28]
Usually unifocalOften multifocal[32,33]
Often preceded by intestinal metaplasiaNo intestinal metaplasia[13,28]
Microsatellite Instability in 15%-20%Lack of MSI[24,29,41-43]
Commonly find loss of heterozygosityInfrequent loss of heterozygosity[24]
COX2 overexpression in 66%COX2 overexpression in 10%[46]
Loss of TFF1 expression in 73%Loss of TFF1 expression in 39%[46]
Loss of RUNX3 geneNo loss of RUNX3[58-61]
Widespread gains throughout genomeGains at chromosomes 17q, 19q and 20q[40]
Distinct gene clusters on hierarchical analysisDistinct gene clusters on hierarchical analysis[39]
Infrequent LMW isoforms of cyclin EFrequent LMW isoforms of cyclin E[52]
CD44v6 expressionCD44v6 more commonly expressed[57]
Usually no family history10% with a family history[13]