TY - JOUR
T1 - Molecular alterations in early gastric carcinomas
T2 - No apparent correlation with Helicobacter pylori status
AU - Blok, Paul
AU - Craanen, Mikael E.
AU - Offerhaus, G. Johan
AU - Dekker, Willem
AU - Kuipers, Ernst J.
AU - Meuwissen, Stephan G.
AU - Tytgat, Guido N.
PY - 1999
Y1 - 1999
N2 - Data on the differences in molecular profile between H pylori-positive and H pylori-negative early gastric carcinomas, if any, are almost nonexistent. We therefore investigated whether molecular differences can be observed between H pylori-positive and H pylori-negative early gastric carcinomas. Forty-five early gastric carcinomas were analyzed for alterations in certain oncogenes (ras, MDM2, c-erbB-2, cyclin D1), the p53 tumor suppressor gene, and the e-cadherin gene. Of these 28 carcinomas were H pylori-positive, and 17 were H pylori-negative. No significant differences were found in the groups irrespective of Lauren type; ras (0% vs 0%), MDM2 (0% vs 0%), c-erbB-2 (0% vs 0%), cyclin D1 (18% vs 29%), p53 (68% vs 47%), and e-cadherin (46% vs 41%). Helicobacter pylori-positive and H pylori- negative early gastric carcinomas do not differ in molecular profile. Although they may prove different when tested for other abnormalities, our findings suggest that the acquisition of molecular alterations occurs via an H pylori independent pathway.
AB - Data on the differences in molecular profile between H pylori-positive and H pylori-negative early gastric carcinomas, if any, are almost nonexistent. We therefore investigated whether molecular differences can be observed between H pylori-positive and H pylori-negative early gastric carcinomas. Forty-five early gastric carcinomas were analyzed for alterations in certain oncogenes (ras, MDM2, c-erbB-2, cyclin D1), the p53 tumor suppressor gene, and the e-cadherin gene. Of these 28 carcinomas were H pylori-positive, and 17 were H pylori-negative. No significant differences were found in the groups irrespective of Lauren type; ras (0% vs 0%), MDM2 (0% vs 0%), c-erbB-2 (0% vs 0%), cyclin D1 (18% vs 29%), p53 (68% vs 47%), and e-cadherin (46% vs 41%). Helicobacter pylori-positive and H pylori- negative early gastric carcinomas do not differ in molecular profile. Although they may prove different when tested for other abnormalities, our findings suggest that the acquisition of molecular alterations occurs via an H pylori independent pathway.
KW - E-cadherin gene
KW - Early gastric carcinoma
KW - Gastric carcinogenesis
KW - Helicobacter pylori
KW - Oncogenes
KW - p53 Tumor suppressor gene
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U2 - 10.1093/ajcp/111.2.241
DO - 10.1093/ajcp/111.2.241
M3 - Article
C2 - 9930147
AN - SCOPUS:0032954882
SN - 0002-9173
VL - 111
SP - 241
EP - 247
JO - American Journal of Clinical Pathology
JF - American Journal of Clinical Pathology
IS - 2
ER -