Aneuploidy of chromosome 8 and C-MYC amplification in individuals from northern Brazil with gastric adenocarcinoma

被引:0
|
作者
Calcagno, DQ
Leal, MF
Takeno, SS
Assumpçao, PP
Demachki, S
Smith, MDC
Burbano, RR
机构
[1] Fed Univ Para, Ctr Ciencias Biol, Dept Biol, Lab Citogenet Humana & Genet Toxicol, BR-66075900 Belem, Para, Brazil
[2] Univ Fed Sao Paulo, Dept Morphol, Discipline Genet, Sao Paulo, SP, Brazil
[3] Fed Univ Para, Joao Barros Barreto Univ Hosp, Dept Pathol, Belem, Para, Brazil
[4] Fed Univ Para, Joao Barros Barreto Univ Hosp, Surg Serv, Belem, Para, Brazil
基金
巴西圣保罗研究基金会;
关键词
fluorescence in situ hybridization; chromosome; 8; aneuploidy; C-MYC amplification; gastric adenocarcinoma;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Gastric cancer is the third most frequent type of neoplasia. In northern Brazil, the State of Para has a high incidence of this type of neoplasia. Limited data are available so far on the genetic events involved in this disease. Materials and Methods: Dual-color fluorescence in situ hybridization (FISH) for the C-MYC gene and chromosome 8 centromere was performed in 11 gastric adenocarcinomas. Results: All cases showed aneuploidy of chromosome 8 and C-MYC amplification, in both the diffuse and the intestinal histopathological types of Lauren. No, correlation was found between polysomy 8 and the histopathological characteristics of the tumors. C-MYC amplification, like homogeneously-stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Translocation of C-MYC was observed only in the diffuse-type. Conclusion: Chromosome 8 can be used as a marker in the diagnosis of gastric adenocarcinoma. The C-WC oncogene requires further studies in order to verify if it is, when amplified, an etiological cause of transformation or a consequence of the proliferation process.
引用
收藏
页码:4069 / 4074
页数:6
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