| Literature DB >> 26311050 |
Dexiang Zhang1, Yuedi Dai2, Yuankun Cai1, Tao Suo3, Han Liu3, Yueqi Wang3, Zhijian Cheng4, Houbao Liu5.
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is one of the most common malignancies in the world. Numerous studies have linked the activation of AKT to the progression of PDAC. Phosphatidylethanolamine-binding protein 4 (PEBP4) has been reported to be upregulated in various cancer types. However, its expression pattern and biological functions in PDAC are unknown. In this study, it was found that the messenger RNA (mRNA) and protein level of PEBP4 was elevated in PDAC samples. Forced expression of PEBP4 in PDAC cell lines promoted cell growth and migration, while downregulation of PEBP4 in PDAC cells by RNA interference (RNAi) inhibited the growth, migration, and metastasis of the cancer cells. PEBP4 interacted with AKT and promoted the phosphorylation of serine 473 in AKT. Collectively, this study suggested that PEBP4 might promote the progression of PDAC through activating AKT signaling and PEBP4 might be a promising therapeutic target for PDAC treatment.Entities:
Keywords: AKT; Cell growth and migration; PDAC; PEBP4
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Year: 2015 PMID: 26311050 DOI: 10.1007/s13277-015-3906-0
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283