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Articles Published Processes
4/7/2016 11:01:00 AM | Browse: 1170 | Download: 1736
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Received |
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2015-06-27 09:11 |
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Peer-Review Started |
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2015-06-30 09:51 |
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To Make the First Decision |
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2015-09-17 13:27 |
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Return for Revision |
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2015-09-25 11:30 |
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Revised |
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2015-11-20 00:52 |
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Second Decision |
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2016-01-27 13:55 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2016-02-16 09:42 |
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Articles in Press |
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2016-02-16 09:42 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2016-03-24 16:21 |
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Publish the Manuscript Online |
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2016-04-07 11:01 |
ISSN |
2218-4333 (online) |
Open Access |
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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Copyright |
© The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
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Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Biochemistry & Molecular Biology |
Manuscript Type |
Editorial |
Article Title |
Targeting Enhancer of Zeste Homolog 2 as a promising strategy for cancer treatment
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Manuscript Source |
Invited Manuscript |
All Author List |
Irene Marchesi and Luigi Bagella |
Funding Agency and Grant Number |
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Corresponding Author |
Luigi Bagella, PhD, Department of Biomedical Sciences, Division of Biochemistry, University of Sassari, Viale S. Pietro 43/b, 07100 Sassari,
Italy. lbagella@uniss.it
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Key Words |
Enhancer of Zeste Homolog 2; Polycomb group proteins; Histone methyltransferase; Enhancer of Zeste Homolog 2 inhibitors; Anticancer drugs; Cancer therapy; Epigenetics |
Core Tip |
Epigenetics modifications are key players in differentiation programs and are frequently altered in cancer. Since chromatin changes can be reversed with specific drugs, in the last years several studies explored the possibility to target epigenetics alteration as a new strategy for cancer treatment. This editorial focuses on Enhancer of Zeste Homolog 2 (EZH2), the catalytic subunit of Polycomb repressive complex 2 in cancer, analyzing different roles of this protein in various cancers. Several different classes of EZH2 inhibitors are also highlighted, giving distinct thoughtfulness to small molecules that are now under consideration as potential candidates for cancer treatment alone or in combination with other drugs. |
Publish Date |
2016-04-07 11:01 |
Citation |
Marchesi I, Bagella L. Targeting Enhancer of Zeste Homolog 2 as a promising strategy for cancer treatment. World J Clin Oncol 2016; 7(2): 135-148 |
URL |
http://www.wjgnet.com/2218-4333/full/v7/i2/135.htm |
DOI |
http://dx.doi.org/10.5306/wjco.v7.i2.135 |
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