ras Gene mutations and expression of Ras signal transduction mediators in gastric adenocarcinomas.

Abstract:

OBJECTIVE:To investigate ras gene alteration in human gastric adenocarcinomas and its potential relationship to ras signal transduction mediators. DESIGN:Genomic DNA from 104 gastric tumors were analyzed by sequencing of polymerase chain reaction-amplified products for the presence of ras mutations. All the samples were further investigated with the use of immunohistochemical analysis for ERK1 and ERK2. SETTING:Tertiary care teaching hospital. PATIENTS:Seventy patients from a Korean population and 34 from a Midwestern US population composed of white Americans and African Americans. RESULTS:Fifteen tumors (14%) were positive for either H-ras or K-ras mutation: 9 (13%) of 70 Korean patients and 6 (18%) of 34 US patients. Seven (78%) of the 9 mutated tumors from Korean patients and all 6 (100%) from the US patients were intestinal-type lesions. Either ERK1 and/or ERK2 was overexpressed in 68 samples (65%). No association was established between ras mutations and overexpression of ERK1/2. However, the correlation between ERK1/2 and progression (early vs late) was statistically significant (P =.007). CONCLUSIONS:These data suggest that ras mutations are uncommon in gastric adenocarcinomas and that differing racial and/or geographic mechanisms may not underlie ras gene alteration. Most ras mutations were, however, observed in the group of intestinal-type samples, supporting the different genetic mechanisms of carcinogenesis between the intestinal- and diffuse-type tumors. It is noteworthy that enhanced ERK1/2 activity could be one of the characteristics of tumor invasiveness in gastric cancers.

journal_name

Arch Pathol Lab Med

authors

Yoo J,Park SY,Robinson RA,Kang SJ,Ahn WS,Kang CS

doi

10.1043/0003-9985(2002)126<1096:RGMAEO>2.0.CO;2

subject

Has Abstract

pub_date

2002-09-01 00:00:00

pages

1096-100

issue

9

eissn

0003-9985

issn

1543-2165

journal_volume

126

pub_type

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