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TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence

BACKGROUND: DNA methyltransferase (DNMT) is one of the major factors mediating the methylation of cancer related genes such as TGF-β receptors (TβRs). This in turn may result in a loss of sensitivity to physiologic levels of TGF-β in aggressive prostate cancer (CaP). The specific mechanisms of DNMT&...

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Autores principales: Zhang, Qiang, Chen, Lin, Helfand, Brian T., Jang, Thomas L., Sharma, Vidit, Kozlowski, James, Kuzel, Timothy Michael, Zhu, Lihua J., Yang, Ximing J., Javonovic, Borko, Guo, Yinglu, Lonning, Scott, Harper, Jay, Teicher, Beverly A., Brendler, Charles, Yu, Nengwang, Catalona, William J., Lee, Chung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184137/
https://www.ncbi.nlm.nih.gov/pubmed/21980391
http://dx.doi.org/10.1371/journal.pone.0025168
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author Zhang, Qiang
Chen, Lin
Helfand, Brian T.
Jang, Thomas L.
Sharma, Vidit
Kozlowski, James
Kuzel, Timothy Michael
Zhu, Lihua J.
Yang, Ximing J.
Javonovic, Borko
Guo, Yinglu
Lonning, Scott
Harper, Jay
Teicher, Beverly A.
Brendler, Charles
Yu, Nengwang
Catalona, William J.
Lee, Chung
author_facet Zhang, Qiang
Chen, Lin
Helfand, Brian T.
Jang, Thomas L.
Sharma, Vidit
Kozlowski, James
Kuzel, Timothy Michael
Zhu, Lihua J.
Yang, Ximing J.
Javonovic, Borko
Guo, Yinglu
Lonning, Scott
Harper, Jay
Teicher, Beverly A.
Brendler, Charles
Yu, Nengwang
Catalona, William J.
Lee, Chung
author_sort Zhang, Qiang
collection PubMed
description BACKGROUND: DNA methyltransferase (DNMT) is one of the major factors mediating the methylation of cancer related genes such as TGF-β receptors (TβRs). This in turn may result in a loss of sensitivity to physiologic levels of TGF-β in aggressive prostate cancer (CaP). The specific mechanisms of DNMT's role in CaP remain undetermined. In this study, we describe the mechanism of TGF-β-mediated DNMT in CaP and its association with clinical outcomes following radical prostatectomy. METHODOLOGY/PRINCIPAL FINDINGS: We used human CaP cell lines with varying degrees of invasive capability to describe how TGF-β mediates the expression of DNMT in CaP, and its effects on methylation status of TGF-β receptors and the invasive capability of CaP in vitro and in vivo. Furthermore, we determined the association between DNMT expression and clinical outcome after radical prostatectomy. We found that more aggressive CaP cells had significantly higher TGF-β levels, increased expression of DNMT, but reduced TβRs when compared to benign prostate cells and less aggressive prostate cancer cells. Blockade of TGF-β signaling or ERK activation (p-ERK) was associated with a dramatic decrease in the expression of DNMT, which results in a coincident increase in the expression of TβRs. Blockade of either TGF-β signaling or DNMT dramatically decreased the invasive capabilities of CaP. Inhibition of TGF-β in an TRAMP-C2 CaP model in C57BL/6 mice using 1D11 was associated with downregulation of DNMTs and p-ERK and impairment in tumor growth. Finally, independent of Gleason grade, increased DNMT1 expression was associated with biochemical recurrence following surgical treatment for prostate cancer. CONCLUSIONS AND SIGNIFICANCE: Our findings demonstrate that CaP derived TGF-β may induce the expression of DNMTs in CaP which is associated with methylation of its receptors and the aggressive potential of CaP. In addition, DNMTs is an independent predictor for disease recurrence after prostatectomy, and may have clinical implications for CaP prognostication and therapy.
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spelling pubmed-31841372011-10-06 TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence Zhang, Qiang Chen, Lin Helfand, Brian T. Jang, Thomas L. Sharma, Vidit Kozlowski, James Kuzel, Timothy Michael Zhu, Lihua J. Yang, Ximing J. Javonovic, Borko Guo, Yinglu Lonning, Scott Harper, Jay Teicher, Beverly A. Brendler, Charles Yu, Nengwang Catalona, William J. Lee, Chung PLoS One Research Article BACKGROUND: DNA methyltransferase (DNMT) is one of the major factors mediating the methylation of cancer related genes such as TGF-β receptors (TβRs). This in turn may result in a loss of sensitivity to physiologic levels of TGF-β in aggressive prostate cancer (CaP). The specific mechanisms of DNMT's role in CaP remain undetermined. In this study, we describe the mechanism of TGF-β-mediated DNMT in CaP and its association with clinical outcomes following radical prostatectomy. METHODOLOGY/PRINCIPAL FINDINGS: We used human CaP cell lines with varying degrees of invasive capability to describe how TGF-β mediates the expression of DNMT in CaP, and its effects on methylation status of TGF-β receptors and the invasive capability of CaP in vitro and in vivo. Furthermore, we determined the association between DNMT expression and clinical outcome after radical prostatectomy. We found that more aggressive CaP cells had significantly higher TGF-β levels, increased expression of DNMT, but reduced TβRs when compared to benign prostate cells and less aggressive prostate cancer cells. Blockade of TGF-β signaling or ERK activation (p-ERK) was associated with a dramatic decrease in the expression of DNMT, which results in a coincident increase in the expression of TβRs. Blockade of either TGF-β signaling or DNMT dramatically decreased the invasive capabilities of CaP. Inhibition of TGF-β in an TRAMP-C2 CaP model in C57BL/6 mice using 1D11 was associated with downregulation of DNMTs and p-ERK and impairment in tumor growth. Finally, independent of Gleason grade, increased DNMT1 expression was associated with biochemical recurrence following surgical treatment for prostate cancer. CONCLUSIONS AND SIGNIFICANCE: Our findings demonstrate that CaP derived TGF-β may induce the expression of DNMTs in CaP which is associated with methylation of its receptors and the aggressive potential of CaP. In addition, DNMTs is an independent predictor for disease recurrence after prostatectomy, and may have clinical implications for CaP prognostication and therapy. Public Library of Science 2011-09-30 /pmc/articles/PMC3184137/ /pubmed/21980391 http://dx.doi.org/10.1371/journal.pone.0025168 Text en Zhang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Qiang
Chen, Lin
Helfand, Brian T.
Jang, Thomas L.
Sharma, Vidit
Kozlowski, James
Kuzel, Timothy Michael
Zhu, Lihua J.
Yang, Ximing J.
Javonovic, Borko
Guo, Yinglu
Lonning, Scott
Harper, Jay
Teicher, Beverly A.
Brendler, Charles
Yu, Nengwang
Catalona, William J.
Lee, Chung
TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title_full TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title_fullStr TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title_full_unstemmed TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title_short TGF-β Regulates DNA Methyltransferase Expression in Prostate Cancer, Correlates with Aggressive Capabilities, and Predicts Disease Recurrence
title_sort tgf-β regulates dna methyltransferase expression in prostate cancer, correlates with aggressive capabilities, and predicts disease recurrence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184137/
https://www.ncbi.nlm.nih.gov/pubmed/21980391
http://dx.doi.org/10.1371/journal.pone.0025168
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