Back to Search Start Over

Negative Association of c-fos Expression as a Favorable Prognostic Indicator in Gastric Cancer

Authors :
Zhou, Li
Zhang, Jie-Shi
Yu, Jian-Chun
Cui, Quan-Cai
Zhou, Wei-Xun
Kang, Wei-Ming
Ma, Zhi-Qiang
Source :
Archives of Medical Research. Apr2010, Vol. 41 Issue 3, p201-206. 6p.
Publication Year :
2010

Abstract

Background and Aims: The onco-protein c-fos was previously linked to favorable prognosis of gastric cancer (GC) without further validations. The present study was designed to address the issue based on a cohort of Chinese patients. Methods: Expression of c-fos was determined by immunohistochemical staining in specimens from 58 patients with GC who underwent surgical resection. The relationships between c-fos expression and clinicopathological and prognostic variables were further evaluated. Results: Expression of c-fos in tumor epithelia was observed in 39 (67.2%) patients. The protein was also positively expressed in lymphocytes within tumors and para-tumor epithelia. Tumors with positive expression of c-fos in tumor epithelia had a smaller size and marginally earlier T stage in all patients and/or those who underwent curative resection. Univariate analysis showed that patients with positive c-fos expression in tumor epithelia had significantly prolonged overall and tumor-free survival. Cox regression analysis revealed that c-fos expression in tumor epithelia was an independent or potential independent indicator of improved prognosis in different subgroups of patients. Expression of c-fos in para-tumor epithelia and intra-tumor lymphocytes was not associated with clinicopathological variables and long-term outcomes in patients. Conclusions: Our data demonstrated that c-fos expression was negatively associated with tumor progression and was predictive for favorable survival in patients with GC. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01884409
Volume :
41
Issue :
3
Database :
Academic Search Index
Journal :
Archives of Medical Research
Publication Type :
Academic Journal
Accession number :
51291835
Full Text :
https://doi.org/10.1016/j.arcmed.2010.04.009