## Abstract __p53__ codon 72, which produces variant proteins with an arginine (Arg) or proline (Pro), has been reported to be associated with cancers of the lung, esophagus and cervix. However, there have been no reports on the __p53__ codon 72 polymorphism in gastric cancer susceptibility in pati
K-ras mutation in helicobacter pylori-associated chronic gastritis in patients with and without gastric cancer
โ Scribed by Toru Hiyama; Ken Haruma; Yasuhiko Kitadai; Hiroshi Masuda; Masaki Miyamoto; Shinji Tanaka; Masaharu Yoshihara; Fumio Shimamoto; Kazuaki Chayama
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- French
- Weight
- 138 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0020-7136
- DOI
- 10.1002/ijc.1644
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โฆ Synopsis
Abstract
Mutations of an oncogene, Kโras, are associated with the development and progression of many types of human cancer. To elucidate the significance of Kโras mutations in gastric carcinogenesis, we examined Kโras mutations in gastric cancers and in Helicobacter pyloriโassociated chronic gastritis (H. pylori__โCG), which is associated with an increased risk for the gastric cancer development. Specimens of gastric cancer and H. pyloriโ__CG were obtained from 64 gastric cancer patients with H. pyloriโCG, 99 cancerโfree H. pyloriโCG patients and 30 H. pyloriโnegative healthy subjects. Kโras mutations were examined by polymerase chain reactionโsingle strand conformation polymorphism (PCRโSSCP), followed by DNA sequencing analysis. Kโras mutations were detected in 4 of 48 (8.3%) gastric cancers, in 10 of 163 (6.1%) H. pyloriโCG and none of the 30 H. pyloriโnegative healthy subjects. In the gastric cancer patients, mutated Kโras was detected in differentiated type cancers but not in any of the undifferentiated type cancers. Kโras mutations in H. pyloriโCG were significantly more frequent in gastric cancer patients than in cancerโfree patients (10.9% vs. 3.0%, p = 0.044). In addition, Kโras mutations in H. pyloriโCG were significantly more frequent in patients with Kโras mutated gastric cancer than in patients with Kโras unmutated gastric cancer (50.0% vs. 3.7%, p = 0.037). These data suggest that the genetic mechanism(s) of carcinogenesis differs between the differentiated type and the undifferentiated type of gastric cancer and that Kโras mutations may be involved in the early stages of gastric carcinogenesis of the differentiated type. ยฉ 2001 WileyโLiss, Inc.
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We conducted a longitudinal cohort study to determine the association of Helicobacter pylori infection and the progression of chronic atrophic gastritis (CAG) with gastric cancer. A cohort of 4655 healthy asymptomatic subjects was followed for a mean period of 7.7 years. H. pylori infection was esta
## Abstract Blood and gastric tissue biopsies of 34 patients with gastritis were tested for the presence of TT virus (TTV), a ubiquitous virus found in the blood of most humans. Thirtyโone of these patients were TTV positive, and 27 patients had virus in both tissues. In addition, 13 of the patient
K-ras mutation appears in about 60% of patients with non-small-cell lung cancer (NSCLC). This freqLency and its presence in normal appearing tissues point to the potential of ras oncogene mutation to serve as a good biomarker. Using enriched PCR (EPCR), which enables the detection of one mutant alle