Targeting Cdc20 as a novel cancer therapeutic strategy
The Anaphase Promoting Complex (APC, also called APC/C) regulates cell cycle progression by forming two closely related, but functionally distinct E3 ubiquitin ligase sub-complexes, APC(Cdc20) and APC(Cdh1), respectively. Emerging evidence has begun to reveal that Cdc20 and Cdh1 have opposing functi...
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Veröffentlicht in: | Pharmacology & therapeutics (Oxford) 2015-07, Vol.151, p.141-151 |
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creator | Wang, Lixia Zhang, Jinfang Wan, Lixin Zhou, Xiuxia Wang, Zhiwei Wei, Wenyi |
description | The Anaphase Promoting Complex (APC, also called APC/C) regulates cell cycle progression by forming two closely related, but functionally distinct E3 ubiquitin ligase sub-complexes, APC(Cdc20) and APC(Cdh1), respectively. Emerging evidence has begun to reveal that Cdc20 and Cdh1 have opposing functions in tumorigenesis. Specifically, Cdh1 functions largely as a tumor suppressor, whereas Cdc20 exhibits an oncogenic function, suggesting that Cdc20 could be a promising therapeutic target for combating human cancer. However, the exact underlying molecular mechanisms accounting for their differences in tumorigenesis remain largely unknown. Therefore, in this review, we summarize the downstream substrates of Cdc20 and the critical functions of Cdc20 in cell cycle progression, apoptosis, ciliary disassembly and brain development. Moreover, we briefly describe the upstream regulators of Cdc20 and the oncogenic role of Cdc20 in a variety of human malignancies. Furthermore, we summarize multiple pharmacological Cdc20 inhibitors including TAME and Apcin, and their potential clinical benefits. Taken together, development of specific Cdc20 inhibitors could be a novel strategy for the treatment of human cancers with elevated Cdc20 expression. |
doi_str_mv | 10.1016/j.pharmthera.2015.04.002 |
format | Article |
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Emerging evidence has begun to reveal that Cdc20 and Cdh1 have opposing functions in tumorigenesis. Specifically, Cdh1 functions largely as a tumor suppressor, whereas Cdc20 exhibits an oncogenic function, suggesting that Cdc20 could be a promising therapeutic target for combating human cancer. However, the exact underlying molecular mechanisms accounting for their differences in tumorigenesis remain largely unknown. Therefore, in this review, we summarize the downstream substrates of Cdc20 and the critical functions of Cdc20 in cell cycle progression, apoptosis, ciliary disassembly and brain development. Moreover, we briefly describe the upstream regulators of Cdc20 and the oncogenic role of Cdc20 in a variety of human malignancies. Furthermore, we summarize multiple pharmacological Cdc20 inhibitors including TAME and Apcin, and their potential clinical benefits. Taken together, development of specific Cdc20 inhibitors could be a novel strategy for the treatment of human cancers with elevated Cdc20 expression.</description><identifier>ISSN: 0163-7258</identifier><identifier>EISSN: 1879-016X</identifier><identifier>DOI: 10.1016/j.pharmthera.2015.04.002</identifier><identifier>PMID: 25850036</identifier><language>eng</language><publisher>England</publisher><subject>Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Apoptosis ; Brain - cytology ; Brain - physiology ; Cdc20 Proteins - antagonists & inhibitors ; Cdc20 Proteins - metabolism ; Cell Cycle ; Cell Differentiation ; Cilia - physiology ; Humans ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Neoplasms - pathology ; Neuronal Plasticity ; Neurons - cytology ; Neurons - physiology ; Ubiquitination</subject><ispartof>Pharmacology & therapeutics (Oxford), 2015-07, Vol.151, p.141-151</ispartof><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>2015 Published by Elsevier Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-8e3c57343b3e97fc8e66a1f5caaa4551716fce38bde220ccc15f184ba0906c9f3</citedby><cites>FETCH-LOGICAL-c490t-8e3c57343b3e97fc8e66a1f5caaa4551716fce38bde220ccc15f184ba0906c9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25850036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Lixia</creatorcontrib><creatorcontrib>Zhang, Jinfang</creatorcontrib><creatorcontrib>Wan, Lixin</creatorcontrib><creatorcontrib>Zhou, Xiuxia</creatorcontrib><creatorcontrib>Wang, Zhiwei</creatorcontrib><creatorcontrib>Wei, Wenyi</creatorcontrib><title>Targeting Cdc20 as a novel cancer therapeutic strategy</title><title>Pharmacology & therapeutics (Oxford)</title><addtitle>Pharmacol Ther</addtitle><description>The Anaphase Promoting Complex (APC, also called APC/C) regulates cell cycle progression by forming two closely related, but functionally distinct E3 ubiquitin ligase sub-complexes, APC(Cdc20) and APC(Cdh1), respectively. Emerging evidence has begun to reveal that Cdc20 and Cdh1 have opposing functions in tumorigenesis. Specifically, Cdh1 functions largely as a tumor suppressor, whereas Cdc20 exhibits an oncogenic function, suggesting that Cdc20 could be a promising therapeutic target for combating human cancer. However, the exact underlying molecular mechanisms accounting for their differences in tumorigenesis remain largely unknown. Therefore, in this review, we summarize the downstream substrates of Cdc20 and the critical functions of Cdc20 in cell cycle progression, apoptosis, ciliary disassembly and brain development. Moreover, we briefly describe the upstream regulators of Cdc20 and the oncogenic role of Cdc20 in a variety of human malignancies. Furthermore, we summarize multiple pharmacological Cdc20 inhibitors including TAME and Apcin, and their potential clinical benefits. Taken together, development of specific Cdc20 inhibitors could be a novel strategy for the treatment of human cancers with elevated Cdc20 expression.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Apoptosis</subject><subject>Brain - cytology</subject><subject>Brain - physiology</subject><subject>Cdc20 Proteins - antagonists & inhibitors</subject><subject>Cdc20 Proteins - metabolism</subject><subject>Cell Cycle</subject><subject>Cell Differentiation</subject><subject>Cilia - physiology</subject><subject>Humans</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Neuronal Plasticity</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>Ubiquitination</subject><issn>0163-7258</issn><issn>1879-016X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkFtLw0AQhRdRbK3-BcmjL4mzt2TzIkjxBgVfKvi2bLaTNCU3d5NC_72prbenAzNnzhk-QgIKEQUa326ibm1c3a_RmYgBlRGICICdkClVSRqOnvdTMh2FhwmTakIuvN8AgBDAzslkHEkAHk9JvDSuwL5simC-sgwC4wMTNO0Wq8CaxqILvlo6HPrSBr53psdid0nOclN5vDrqjLw9Piznz-Hi9ellfr8IrUihDxVyKxMueMYxTXKrMI4NzaU1xggpaULj3CJX2QoZA2stlTlVIjOQQmzTnM_I3SG3G7IaVxab8YFKd66sjdvp1pT6_6Yp17pot1oImciUjgE3xwDXfgzoe12X3mJVmQbbwWuaAOVUxZKNVnWwWtd67zD_qaGg99j1Rv9i13vsGoQesY-n13_f_Dn85sw_ATlmgv4</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Wang, Lixia</creator><creator>Zhang, Jinfang</creator><creator>Wan, Lixin</creator><creator>Zhou, Xiuxia</creator><creator>Wang, Zhiwei</creator><creator>Wei, Wenyi</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150701</creationdate><title>Targeting Cdc20 as a novel cancer therapeutic strategy</title><author>Wang, Lixia ; Zhang, Jinfang ; Wan, Lixin ; Zhou, Xiuxia ; Wang, Zhiwei ; Wei, Wenyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-8e3c57343b3e97fc8e66a1f5caaa4551716fce38bde220ccc15f184ba0906c9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Apoptosis</topic><topic>Brain - cytology</topic><topic>Brain - physiology</topic><topic>Cdc20 Proteins - antagonists & inhibitors</topic><topic>Cdc20 Proteins - metabolism</topic><topic>Cell Cycle</topic><topic>Cell Differentiation</topic><topic>Cilia - physiology</topic><topic>Humans</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Neuronal Plasticity</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Ubiquitination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Lixia</creatorcontrib><creatorcontrib>Zhang, Jinfang</creatorcontrib><creatorcontrib>Wan, Lixin</creatorcontrib><creatorcontrib>Zhou, Xiuxia</creatorcontrib><creatorcontrib>Wang, Zhiwei</creatorcontrib><creatorcontrib>Wei, Wenyi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pharmacology & therapeutics (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Lixia</au><au>Zhang, Jinfang</au><au>Wan, Lixin</au><au>Zhou, Xiuxia</au><au>Wang, Zhiwei</au><au>Wei, Wenyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting Cdc20 as a novel cancer therapeutic strategy</atitle><jtitle>Pharmacology & therapeutics (Oxford)</jtitle><addtitle>Pharmacol Ther</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>151</volume><spage>141</spage><epage>151</epage><pages>141-151</pages><issn>0163-7258</issn><eissn>1879-016X</eissn><abstract>The Anaphase Promoting Complex (APC, also called APC/C) regulates cell cycle progression by forming two closely related, but functionally distinct E3 ubiquitin ligase sub-complexes, APC(Cdc20) and APC(Cdh1), respectively. Emerging evidence has begun to reveal that Cdc20 and Cdh1 have opposing functions in tumorigenesis. Specifically, Cdh1 functions largely as a tumor suppressor, whereas Cdc20 exhibits an oncogenic function, suggesting that Cdc20 could be a promising therapeutic target for combating human cancer. However, the exact underlying molecular mechanisms accounting for their differences in tumorigenesis remain largely unknown. Therefore, in this review, we summarize the downstream substrates of Cdc20 and the critical functions of Cdc20 in cell cycle progression, apoptosis, ciliary disassembly and brain development. Moreover, we briefly describe the upstream regulators of Cdc20 and the oncogenic role of Cdc20 in a variety of human malignancies. Furthermore, we summarize multiple pharmacological Cdc20 inhibitors including TAME and Apcin, and their potential clinical benefits. Taken together, development of specific Cdc20 inhibitors could be a novel strategy for the treatment of human cancers with elevated Cdc20 expression.</abstract><cop>England</cop><pmid>25850036</pmid><doi>10.1016/j.pharmthera.2015.04.002</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Apoptosis Brain - cytology Brain - physiology Cdc20 Proteins - antagonists & inhibitors Cdc20 Proteins - metabolism Cell Cycle Cell Differentiation Cilia - physiology Humans Neoplasms - drug therapy Neoplasms - metabolism Neoplasms - pathology Neuronal Plasticity Neurons - cytology Neurons - physiology Ubiquitination |
title | Targeting Cdc20 as a novel cancer therapeutic strategy |
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