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https://hdl.handle.net/2440/77731
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Type: | Journal article |
Title: | Dual roles of PARP-1 promote cancer growth and progression |
Author: | Schiewer, M. Goodwin, J. Han, S. Brenner, J. Augello, M. Dean, J. Liu, F. Planck, J. Ravindranathan, P. Chinnaiyan, A. McCue, P. Gomella, L. Raj, G. Dicker, A. Brody, J. Pascal, J. Centenera, M. Butler, L. Tilley, W. Feng, F. et al. |
Citation: | Cancer Discovery, 2012; 2(12):1134-1149 |
Publisher: | American Association for Cancer Research |
Issue Date: | 2012 |
ISSN: | 2159-8274 2159-8290 |
Statement of Responsibility: | Matthew J. Schiewer, Jonathan F. Goodwin, Sumin Han, J. Chad Brenner, Michael A. Augello, Jeffry L. Dean, Fengzhi Liu, Jamie L. Planck, Preethi Ravindranathan, Arul M. Chinnaiyan, Peter McCue, Leonard G. Gomella, Ganesh V. Raj, Adam P. Dicker, Jonathan R. Brody, John M. Pascal, Margaret M. Centenera, Lisa M. Butler, Wayne D. Tilley, Felix Y. Feng and Karen E. Knudsen |
Abstract: | <h4>Unlabelled</h4>PARP-1 is an abundant nuclear enzyme that modifies substrates by poly(ADP-ribose)-ylation. PARP-1 has well-described functions in DNA damage repair and also functions as a context-specific regulator of transcription factors. With multiple models, data show that PARP-1 elicits protumorigenic effects in androgen receptor (AR)-positive prostate cancer cells, in both the presence and absence of genotoxic insult. Mechanistically, PARP-1 is recruited to sites of AR function, therein promoting AR occupancy and AR function. It was further confirmed in genetically defined systems that PARP-1 supports AR transcriptional function, and that in models of advanced prostate cancer, PARP-1 enzymatic activity is enhanced, further linking PARP-1 to AR activity and disease progression. In vivo analyses show that PARP-1 activity is required for AR function in xenograft tumors, as well as tumor cell growth in vivo and generation and maintenance of castration resistance. Finally, in a novel explant system of primary human tumors, targeting PARP-1 potently suppresses tumor cell proliferation. Collectively, these studies identify novel functions of PARP-1 in promoting disease progression, and ultimately suggest that the dual functions of PARP-1 can be targeted in human prostate cancer to suppress tumor growth and progression to castration resistance.<h4>Significance</h4>These studies introduce a paradigm shift with regard to PARP-1 function in human malignancy, and suggest that the dual functions of PARP-1 in DNA damage repair and transcription factor regulation can be leveraged to suppress pathways critical for promalignant phenotypes in prostate cancer cells by modulation of the DNA damage response and hormone signaling pathways. The combined studies highlight the importance of dual PARP-1 function in malignancy and provide the basis for therapeutic targeting. |
Keywords: | Cell Line, Tumor Chromatin Animals Mice, Inbred BALB C Humans Mice Mice, Nude Prostatic Neoplasms DNA Damage Disease Progression Benzimidazoles Poly(ADP-ribose) Polymerases Receptors, Androgen Cell Growth Processes Male Poly(ADP-ribose) Polymerase Inhibitors Poly (ADP-Ribose) Polymerase-1 |
Rights: | Copyright © 2012 American Association for Cancer Research |
DOI: | 10.1158/2159-8290.CD-12-0120 |
Published version: | http://dx.doi.org/10.1158/2159-8290.cd-12-0120 |
Appears in Collections: | Aurora harvest 4 Medicine publications |
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