Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/80807
Title: Discovery of a small-molecule binder of the oncoprotein gankyrin that modulates gankyrin activity in the cell
Authors: Chattopadhyay, Anasuya
O’Connor, Cornelius J.
Zhang, Fengzhi
Galvagnion, Celine
Galloway, Warren R. J. D.
Tan, Yaw Sing
Stokes, Jamie E.
Rahman, Taufiq
Verma, Chandra
Spring, David R.
Itzhaki, Laura S.
Keywords: DNA Damage
DRNTU::Science::Biological sciences
Cell Cycle Protein
Issue Date: 2016
Source: Chattopadhyay, A., O’Connor, C. J., Zhang, F., Galvagnion, C., Galloway, W. R. J. D., Tan, Y. S., . . . Itzhaki, L. S. (2016). Discovery of a small-molecule binder of the oncoprotein gankyrin that modulates gankyrin activity in the cell. Scientific Reports, 6, 23732-. doi:10.1038/srep23732
Series/Report no.: Scientific Reports
Abstract: Gankyrin is an ankyrin-repeat oncoprotein whose overexpression has been implicated in the development of many cancer types. Elevated gankyrin levels are linked to aberrant cellular events including enhanced degradation of tumour suppressor protein p53, and inhibition of gankyrin activity has therefore been identified as an attractive anticancer strategy. Gankyrin interacts with several partner proteins, and a number of these protein-protein interactions (PPIs) are of relevance to cancer. Thus, molecules that bind the PPI interface of gankyrin and interrupt these interactions are of considerable interest. Herein, we report the discovery of a small molecule termed cjoc42 that is capable of binding to gankyrin. Cell-based experiments demonstrate that cjoc42 can inhibit gankyrin activity in a dose-dependent manner: cjoc42 prevents the decrease in p53 protein levels normally associated with high amounts of gankyrin, and it restores p53-dependent transcription and sensitivity to DNA damage. The results represent the first evidence that gankyrin is a “druggable” target with small molecules.
URI: https://hdl.handle.net/10356/80807
http://hdl.handle.net/10220/46601
DOI: 10.1038/srep23732
Rights: © 2016 The Authors (Nature Publishing Group). This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles

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