| Literature DB >> 29575012 |
Shaohua Fan1, Yanyan Wang2, Zifeng Zhang1, Jun Lu1, Zhiyong Wu3, Qun Shan1, Chunhui Sun1, Dongmei Wu2, Mengqiu Li1, Ning Sheng1, Ying Xie1, Yuanlin Zheng1.
Abstract
Glutamate-ammonia ligase (GLUL), which is also called GS (glutamine synthetase), is the enzyme that catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. Here, we found higher expression of GLUL in the ovarian cancer patients was associated with worse disease-free survival (DFS) and overall survival (OS). In addition, GLUL was heterogeneously expressed in various ovarian cancer cells. The mRNA and protein expression levels of GLUL in NIH:OVCAR-3 and ES-2 cells were obviously higher than that in the other types of ovarian cancer cells. Knockdown of GLUL in NIH:OVCAR-3 or ES-2 cells could significantly decrease the proliferation ability. Furthermore, GLUL knockdown markedly inhibited the p38 MAPK signaling pathway in NIH:OVCAR-3 or ES-2 cells. Our findings suggest that decreasing expression of GLUL may be a new approach that can be used for ovarian cancer treatment.Entities:
Keywords: glutamate-ammonia ligase; ovarian cancer; proliferation
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Year: 2018 PMID: 29575012 DOI: 10.1002/jcb.26797
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429