Abstract | BACKGROUND: MATERIALS AND METHODS: INPP4B expression data were obtained from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. Clinicopathological and survival data were retrieved from the TCGA database. CCK8 and colony formation assays were performed to measure the proliferative capacity of pancreatic cancer. Tumor xenograft models were established to measure cancer proliferative abilities in vivo. RESULTS: INPP4B was upregulated in pancreatic cancer tissue compared with normal tissue. INPP4B knockdown inhibited cell proliferation and promoted apoptosis in pancreatic cancer in vitro and in vivo. INPP4B knockdown also reduced AKT phosphorylation. Moreover, INPP4B was associated with poor overall and disease-free survival, with Cox regression analysis showing that INPP4B could serve as an independent prognostic marker. ROC curve analysis showed that INPP4B possessed moderate diagnostic value. CONCLUSION: Collectively, INPP4B is an oncogenic gene in pancreatic cancer and could serve as a potential diagnostic marker and an independent prognostic marker, suggesting that it could be a novel therapeutic target for pancreatic cancer.
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Authors | Shuyu Zhai, Yuanbin Liu, Xiongxiong Lu, Hao Qian, Xiaomei Tang, Xi Cheng, Yue Wang, Yusheng Shi, Xiaxing Deng |
Journal | OncoTargets and therapy
(Onco Targets Ther)
Vol. 12
Pg. 8287-8299
( 2019)
ISSN: 1178-6930 [Print] New Zealand |
PMID | 31632078
(Publication Type: Journal Article)
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Copyright | © 2019 Zhai et al. |