Please use this identifier to cite or link to this item: https://doi.org/10.7150/jca.25138
Title: Functional genome-wide screening identifies targets and pathways sensitizing pancreatic cancer cells to dasatinib
Authors: Chien W. 
Sudo M. 
Ding L.-W. 
Sun Q.-Y. 
Wuensche P.
Lee K.L. 
Hattori N.
Garg M. 
Xu L. 
Zheng Y.
Gery S.
Wongphayak S. 
Yang H. 
Baloglu E.
Shacham S.
Kauffman M.
Mori S. 
Phillip Koeffler H.
Keywords: Dasatinib
Pancreatic Cancer
XPO
Issue Date: 2018
Publisher: Ivyspring International Publisher
Citation: Chien W., Sudo M., Ding L.-W., Sun Q.-Y., Wuensche P., Lee K.L., Hattori N., Garg M., Xu L., Zheng Y., Gery S., Wongphayak S., Yang H., Baloglu E., Shacham S., Kauffman M., Mori S., Phillip Koeffler H. (2018). Functional genome-wide screening identifies targets and pathways sensitizing pancreatic cancer cells to dasatinib. Journal of Cancer 9 (24) : 4762-4773. ScholarBank@NUS Repository. https://doi.org/10.7150/jca.25138
Abstract: This study is an unbiased genomic screen to obtain functional targets for increased effectiveness of dasatinib in pancreatic cancer. Dasatinib, a multi-targeted tyrosine kinase inhibitor, is used in clinical trials for treatment of pancreatic cancer; however, intrinsic and acquired resistance often occurs. We used a dasatinib-resistant pancreatic cancer cell line SU8686 to screen for synthetic lethality that synergizes with dasatinib using a pooled human shRNA library followed by next generation sequencing. Novel genes were identified which when silenced produced a prominent inhibitory effect with dasatinib against the pancreatic cancer cells. Several of these genes are involved in the regulation of epigenetics, as well as signaling pathways of the FOXO and hedgehog families. Small molecule inhibitors of either histone deacetylases or nuclear exporter had marked inhibitory effect with dasatinib in pancreatic cancers, suggesting their potential therapeutic effectiveness in this deadly cancer. � Ivyspring International Publisher. This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license
Source Title: Journal of Cancer
URI: https://scholarbank.nus.edu.sg/handle/10635/164164
ISSN: 18379664
DOI: 10.7150/jca.25138
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