scholarly journals S57 Identification of Two Upregulated Genes in Tumor Tissues With Poor Prognosis in Pancreatic Ductal Adenocarcinoma via Bioinformatical Analysis

2021 ◽  
Vol 116 (1) ◽  
pp. S24-S25
Author(s):  
Chenyu Sun ◽  
Yuting Huang ◽  
John Pocholo W. Tuason ◽  
Na Hyun Kim ◽  
Chandur Bhan ◽  
...  
2021 ◽  
Vol 116 (1) ◽  
pp. S654-S655
Author(s):  
Chenyu Sun ◽  
Na Hyun Kim ◽  
John Pocholo W. Tuason ◽  
Ce Cheng ◽  
Chandur Bhan ◽  
...  

Cancer ◽  
2006 ◽  
Vol 107 (2) ◽  
pp. 251-257 ◽  
Author(s):  
Norihiro Sato ◽  
Noriyoshi Fukushima ◽  
Hiroyuki Matsubayashi ◽  
Christine A. Iacobuzio-Donahue ◽  
Charles J. Yeo ◽  
...  

Tumor Biology ◽  
2015 ◽  
Vol 36 (12) ◽  
pp. 9189-9199 ◽  
Author(s):  
Chen Gong ◽  
Yixin Zhang ◽  
Yinji Chen ◽  
Haifeng Zhang ◽  
Xiaorong Liu ◽  
...  

2021 ◽  
Author(s):  
Hao Yu ◽  
Xiaoping Mei ◽  
Xueming Zhang ◽  
Neng Qian ◽  
Qingjiang Yu ◽  
...  

Abstract Objective: Pancreatic ductal adenocarcinoma (PDAC) serves as a prevailing tumor type with high mortality and poor prognosis. The study aims to explore the mechanism of gemcitabine resistance in PDAC patients. Methods: Immunohistochemistry(IHC)was used to analyze the expression of SLC39A1 in PDAC samples. PDAC cells were culture and transfected with siSLC39A1 and siNC, respectively. Cell proliferation analysis was performed using CCK-8 assay. And qPCR and Western blotting was used to analysis the expression level of SLC39A1 and related signal molecular in cells. Results: IHC results demonstrated that the SLC39A1 expression was significantly up-regulated in the gemcitabine-resistant PDAC samples compared with gemcitabine-sensitive PDAC samples. The treatment of gemcitabine dose-dependently inhibited the viability of the PDAC cells. Meanwhile, the mRNA and protein expression of SLC39A1 were elevated in the gemcitabine-resistant PDAC. The treatment of gemcitabine remarkably decreased viability of PDACs, in which SLC39A1 depletion could reverse this effect. SLC39A1 knockdown could reverse the gemcitabine-induced phosphorylation of AMPK enhanced and gemcitabine-inhibited S6K expression. Conclusion: SLC39A1 contributed to gemcitabine resistance of PDAC by activating AMPK signaling.


Pancreatology ◽  
2019 ◽  
Vol 19 (3) ◽  
pp. 443-448 ◽  
Author(s):  
Yuki Hashimoto ◽  
Mitsuaki Ishida ◽  
Hironori Ryota ◽  
Tomohisa Yamamoto ◽  
Hisashi Kosaka ◽  
...  

2020 ◽  
Vol 123 (1) ◽  
pp. 72-80
Author(s):  
Fabien Robin ◽  
Gaëlle Angenard ◽  
Luis Cano ◽  
Laetitia Courtin-Tanguy ◽  
Elodie Gaignard ◽  
...  

2020 ◽  
Vol 11 (8) ◽  
pp. 2213-2221
Author(s):  
Ming Cui ◽  
Lei You ◽  
Bang Zheng ◽  
Xinmei Huang ◽  
Qiaofei Liu ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Tao Sun ◽  
Xiangyu Kong ◽  
Yiqi Du ◽  
Zhaoshen Li

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with a high rate of mortality and poor prognosis. Numerous studies have proved that microRNA (miRNA) may play a vital role in a wide range of malignancies, including PDAC, and dysregulated miRNAs, including circulating miRNAs, are associated with PDAC proliferation, invasion, chemosensitivity, and radiosensitivity, as well as prognosis. Greater understanding of the roles of miRNAs in PDAC could provide insights into this disease and identify potential diagnostic markers and therapeutic targets. The current review focuses on recent advances with respect to the roles of miRNAs in PDAC and their practical value.


2016 ◽  
Vol 73 (4) ◽  
pp. 152-157 ◽  
Author(s):  
BoLin Sun ◽  
Xiaogang Liu ◽  
Yewu Gao ◽  
Li Li ◽  
ZhenLing Dong

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