| Literature DB >> 26520441 |
Zhendong Zheng1,2, Yingjuan Zheng3, Meiyan Zhang4, Jiejun Wang5,6, Guanzhen Yu7,8, Wenzheng Fang9.
Abstract
Activation of AMP-activated protein kinase (AMPK) suppressed mammalian target of rapamycin (mTOR) pathway, resulting in impaired cancer cell proliferation. Two cohorts (50 and 1072 cases) of patients with resected gastric adenocarcinoma were enrolled in the study. Immunohistochemical staining for p-AMPKa, p-ACC, p-mTOR, p-S6, and p-4EBP1 was performed on the 50-patient cohort. Tissue microarray blocks containing samples from 1072 patients of Chinese ethnicity were used for the immunohistochemical detection of p-AMPKa and p-S6 levels. p-AMPK and p-ACC were frequently inactivated in both cohorts of gastric cancer samples, while p-mTOR, p-S6, and p-4EBP1 were frequently activated in the small cohort of gastric cancer. However, only levels of p-AMPKa and p-S6 were associated with the overall survival of gastric cancer patients. In the larger 1072-patient cohort, downregulation of p-AMPKa and upregulation of p-S6 were associated with tumor progression and were independent predictors of survival after resection of primary gastric cancer. Therefore, reciprocal expression of p-AMPKa and p-S6 may be promising prognostic biomarkers in patients with gastric cancer.Entities:
Keywords: Gastric carcinoma; Immunohistochemistry; Prognosis; p-4EBP1; p-ACC; p-AMPKa; p-S6; p-mTOR
Mesh:
Substances:
Year: 2015 PMID: 26520441 DOI: 10.1007/s13277-015-4193-5
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283