Gene Expression in Gastric Adenocarcinomas

위선암에서의 유전자 발현

  • Lee Jong Hoon (Departments of Internal Medicine Departments of Internal Medicine) ;
  • Choi Seok Ryeol (Departments of Internal Medicine Departments of Internal Medicine) ;
  • Han Sang Young (Departments of Internal Medicine Departments of Internal Medicine) ;
  • Hwang Tae Ho (Departments of Pharmacology) ;
  • Kim Min Chan (Departments of Departments of Internal Medicine) ;
  • Jung Ghap Joong (Departments of Departments of Internal Medicine) ;
  • Roh Mee Sook (Departments of Pathology, Departments of Internal Medicine) ;
  • Jeong Jin Sook (Departments of Pathology, Departments of Internal Medicine)
  • 이종훈 (동아대학교 의과대학 내과학교실) ;
  • 최석렬 (동아대학교 의과대학 내과학교실) ;
  • 한상영 (동아대학교 의과대학 내과학교실) ;
  • 황태호 (동아대학교 의과대학 약리학교실) ;
  • 김민찬 (동아대하교 의과대학 외과학교실) ;
  • 정갑중 (동아대학교 의과대학 외과학교실) ;
  • 노미숙 (동아대학교 의과대학 병리학교실) ;
  • 정진숙 (동아대학교 의과대학 병리학교실)
  • Published : 2002.12.01

Abstract

Purpose: The cDNA microarray provides a powerful alternative with an unprecedented view in monitoring geneexpression levels and leads to discoveries of regulatory pathways involved in complicated biological processes. Our aim is to explore the different gene-expression patterns in gastric adenocarcinomas. Materials and Methods: By using a cDNA microarray representing 4,600 cDNA clusters, we studied the expression profiling in 10 paired gastric adenocarcinoma samples and in adjacent noncancerous gastric tissues from the same patients. Alterations in the gene-expression levels were confirmed by Vsing Northern blots and reverse-transcription PCR (RT-PCR) in all of 4 randomly selected genes. Results: Genes those were expressed differently in cancer ous and noncancerous tissues were identified. 44 (of which 26 were known) and 92 (of which 43 were known) genes or cDNA were up- and down-regulated, respectively, in more than $80\%$ of the gastric adenocarcinoma samples. In cancer ous tissues, genes related to gene/protein expression, cellcycle regulation, and metabolism were mostly up-regulated whereas genes related to the oncogene/tumor suppressor gene, cell structure/motility, and immunology were mostly down-regulated. The semi-quantitative RT-PCR results for the four genes we tested were consistent with the array findings. Conclusions: These results provide not only a new molecular basis for understanding the biological properties of gastric adenocarcinomas but also a useful resource for future development of therapeutic targets and diagnostic markers for gastric adenocarcinomas.

Keywords