Amplification of the UQCRFS1 Gene in Gastric Cancers.
- Author:
Kyong Hwa JUN
1
;
Su Young KIM
;
Jung Hwan YOON
;
Jae Hwi SONG
;
Won Sang PARK
Author Information
- Publication Type:Original Article
- Keywords: Stomach neoplasms; ArrayCGH; Immunohistochemistry; Amplification; Overexpression
- MeSH: Adenocarcinoma; Cell Line; Coat Protein Complex I; DNA; DNA Copy Number Variations; Immunohistochemistry; Nucleic Acid Hybridization; Real-Time Polymerase Chain Reaction; Stomach Neoplasms
- From:Journal of Gastric Cancer 2012;12(2):73-80
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: The specific aim of this study is to unravel a DNA copy number alterations, and to search for novel genes that are associated with the development of Korean gastric cancer. MATERIALS AND METHODS: We investigated a DNA copy number changes in 23 gastric adenocarcinomas by array-comparative genomic hybridization and quantitative real-time polymerase chain reaction analyses. Besides, the expression of UQCRFS1, which shows amplification in array-CGH, was examined in 186 gastric cancer tissues by an immunohistochemistry, and in 9 gastric cancer cell lines, as well as 24 gastric cancer tissues by immunoblotting. RESULTS: We found common gains at 48 different loci, and a common loss at 19 different loci. Amplification of UQCRFS1 gene at 19q12 was found in 5 (21.7%) of the 23 gastric cancers in an array-comparative genomic hybridization and DNA copy number were increased in 5 (20.0%) out of the 25 gastric cancer in quantitative real-time polymerase chain reaction. In immunohistochemistry, the overexpression of the protein was detected in 105 (56.5%) out of the 186 gastric cancer tissues. Statistically, there was no significant relationship between the overexpression of UQCRFS1 and clinicopathologic parameters (P>0.05). In parallel, the overexpression of UQCRFS1 protein was confirmed in 6 (66.7%) of the 9 gastric cancer cell lines, and 12 (50.0%) of the 24 gastric cancer tissues by immunoblotting. CONCLUSIONS: These results suggest that the overexpression of UQCRFS1 gene may contribute to the development and/or progression of gastric cancer, and further supported that mitochondrial change may serve as a potential cancer biomarker.
