Literature DB >> 15389513

Preoperative genetic diagnosis of gastric carcinoma based on chromosomal loss and microsatellite instability.

Seung-Jin Hong1, Sang-Wook Choi, Kang-Hoon Lee, Sung Lee, Ki-Ouk Min, Mun-Gan Rhyu.   

Abstract

The degree of chromosomal losses and the presence of microsatellite instability (MSI) in gastric carcinomas have been categorized into low-risk (low-level loss and MSI) and high-risk (baseline- and high-level losses) genotypes. With the aim of making a preoperative diagnosis, this study confirmed the stem line genotype that is common over an entire tumor as well as in a single biopsy specimen. Biopsy specimens were obtained from 91 gastric carcinoma patients and examined for their microsatellite genotypes using a panel of 41 microsatellite markers on 8 cancer-associated chromosomes. The genotype of the biopsy specimens was compared with that of a surgical specimen, which had been multifocally examined for its intratumoral heterogeneity. Of the 91 pairs of biopsy and surgical specimens, 87 (96%) containing either the same (60 cases) or a similar (17 cases) number of chromosomal losses were categorized into the same microsatellite genotype, and the remaining 4 pairs (4%) were classified into a different genotype. The surgical specimens showed that an extraserosal invasion and lymph node metastasis are frequently associated with either a high-level (4 or more) of chromosomal losses irrespective of the tumor size (73% and 85%) or the large carcinomas > 5 cm in diameter irrespective of the tumor genotype (76% and 83%). The status of the extraserosal invasion and lymph node metastasis (0.691 and 0.802 receiver operating characteristic areas, respectively) predicted by the biopsy genotype and the tumor size corresponded closely to the surgical pathology results. Therefore, the extent of chromosomal losses and the presence of an MSI determined on a biopsy specimen will provide valuable information for making a preoperative genetic diagnosis of a gastric carcinoma.

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Year:  2005        PMID: 15389513     DOI: 10.1002/ijc.20603

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  5 in total

1.  Relationship between the extent of chromosomal losses and the pattern of CpG methylation in gastric carcinomas.

Authors:  Seung-Jin Hong; Young-Ho Kim; Young-Deok Choi; Ki-Ouk Min; Sang-Wook Choi; Mun-Gan Rhyu
Journal:  J Korean Med Sci       Date:  2005-10       Impact factor: 2.153

2.  The overmethylated genes in Helicobacter pylori-infected gastric mucosa are demethylated in gastric cancers.

Authors:  Seung-Jin Hong; Jung-Hwan Oh; Eun-Jung Jeon; Ki-Ouk Min; Moo-Il Kang; Sang-Wook Choi; Mun-Gan Rhyu
Journal:  BMC Gastroenterol       Date:  2010-11-20       Impact factor: 3.067

3.  The gene-reduction effect of chromosomal losses detected in gastric cancers.

Authors:  Seung-Jin Hong; Eun-Jung Jeon; Jung-Hwan Oh; Eun-Joo Seo; Sang-Wook Choi; Mun-Gan Rhyu
Journal:  BMC Gastroenterol       Date:  2010-11-20       Impact factor: 3.067

4.  The 5'-end transitional CpGs between the CpG islands and retroelements are hypomethylated in association with loss of heterozygosity in gastric cancers.

Authors:  Young-Ho Kim; Seung-Jin Hong; Yu-Chae Jung; Sung-Ja Kim; Eun-Joo Seo; Sang-Wook Choi; Mun-Gan Rhyu
Journal:  BMC Cancer       Date:  2006-07-10       Impact factor: 4.430

5.  Chromosomal losses are associated with hypomethylation of the gene-control regions in the stomach with a low number of active genes.

Authors:  Yu-Chae Jung; Seung-Jin Hong; Young-Ho Kim; Sung-Ja Kim; Seok-Jin Kang; Sang-Wook Choi; Mun-Gan Rhyu
Journal:  J Korean Med Sci       Date:  2008-12-24       Impact factor: 2.153

  5 in total

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