The Mitotic Checkpoint in Cancer Therapy
The mitotic checkpoint is a key cell cycle control mechanism that ensures an accurate segregation of chromosomes during mitosis by delaying the onset of anaphase until all chromosomes are properly attached to a bipolar mitotic spindle. While complete loss of this checkpoint is lethal in vertebrates,...
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Veröffentlicht in: | Cell cycle (Georgetown, Tex.) Tex.), 2005-11, Vol.4 (11), p.1495-1499 |
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description | The mitotic checkpoint is a key cell cycle control mechanism that ensures an accurate segregation of chromosomes during mitosis by delaying the onset of anaphase until all chromosomes are properly attached to a bipolar mitotic spindle. While complete loss of this checkpoint is lethal in vertebrates, a weakened mitotic checkpoint is frequently seen in cancer cells and it may contribute to tumorigenesis. Many antitumor drugs, including spindle assembly inhibitors and DNA damaging agents, can activate the mitotic checkpoint. However, since these drugs influence interphase events besides activating the mitotic checkpoint, the role of the mitotic checkpoint in drug-induced cell death remained unclear. Using a KSP antagonist that specifically acts on mitotic cells, we have recently shown that activation of the mitotic checkpoint followed by mitotic slippage or adaptation, activates Bax and initiates apoptosis. Notably, cells with a weakened mitotic checkpoint incur much less apoptotic death than their checkpoint-proficient counterparts, indicating the requirement of a competent mitotic checkpoint in the induction of apoptosis. In light of these findings and other recent reports, the potential influence of the mitotic checkpoint in response to chemotherapies, and the strategy to target the mitotic checkpoint for cancer therapeutics are discussed. |
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While complete loss of this checkpoint is lethal in vertebrates, a weakened mitotic checkpoint is frequently seen in cancer cells and it may contribute to tumorigenesis. Many antitumor drugs, including spindle assembly inhibitors and DNA damaging agents, can activate the mitotic checkpoint. However, since these drugs influence interphase events besides activating the mitotic checkpoint, the role of the mitotic checkpoint in drug-induced cell death remained unclear. Using a KSP antagonist that specifically acts on mitotic cells, we have recently shown that activation of the mitotic checkpoint followed by mitotic slippage or adaptation, activates Bax and initiates apoptosis. Notably, cells with a weakened mitotic checkpoint incur much less apoptotic death than their checkpoint-proficient counterparts, indicating the requirement of a competent mitotic checkpoint in the induction of apoptosis. In light of these findings and other recent reports, the potential influence of the mitotic checkpoint in response to chemotherapies, and the strategy to target the mitotic checkpoint for cancer therapeutics are discussed.</description><identifier>ISSN: 1538-4101</identifier><identifier>EISSN: 1551-4005</identifier><identifier>DOI: 10.4161/cc.4.11.2130</identifier><identifier>PMID: 16258280</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Animals ; Antimitotic Agents - therapeutic use ; Antineoplastic Agents - therapeutic use ; Apoptosis - drug effects ; Apoptosis - physiology ; Binding ; Biology ; Bioscience ; Calcium ; Cancer ; Cell ; Cycle ; Humans ; Landes ; Mitosis - drug effects ; Mitosis - physiology ; Neoplasms - drug therapy ; Neoplasms - pathology ; Organogenesis ; Proteins</subject><ispartof>Cell cycle (Georgetown, Tex.), 2005-11, Vol.4 (11), p.1495-1499</ispartof><rights>Copyright © 2005 Landes Bioscience 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-a5f0a3bb9744b7f589c9553d91971a4f4146095573fdac03432c5e454e1262133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16258280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tao, Weikang</creatorcontrib><title>The Mitotic Checkpoint in Cancer Therapy</title><title>Cell cycle (Georgetown, Tex.)</title><addtitle>Cell Cycle</addtitle><description>The mitotic checkpoint is a key cell cycle control mechanism that ensures an accurate segregation of chromosomes during mitosis by delaying the onset of anaphase until all chromosomes are properly attached to a bipolar mitotic spindle. 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In light of these findings and other recent reports, the potential influence of the mitotic checkpoint in response to chemotherapies, and the strategy to target the mitotic checkpoint for cancer therapeutics are discussed.</description><subject>Animals</subject><subject>Antimitotic Agents - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - physiology</subject><subject>Binding</subject><subject>Biology</subject><subject>Bioscience</subject><subject>Calcium</subject><subject>Cancer</subject><subject>Cell</subject><subject>Cycle</subject><subject>Humans</subject><subject>Landes</subject><subject>Mitosis - drug effects</subject><subject>Mitosis - physiology</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Organogenesis</subject><subject>Proteins</subject><issn>1538-4101</issn><issn>1551-4005</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkLtPwzAQhy0EoqWwMaNMiIGkPj_yGFHESypiKbPlOI5qSOJgp0L973GVAguTT9Z3v7v7ELoEnDBIYalUwhKAhADFR2gOnEPMMObH-5rmMQMMM3Tm_TvGJM8KOEUzSAnPSY7n6Ga90dGLGe1oVFRutPoYrOnHyPRRKXulXRQAJ4fdOTppZOv1xeFdoLeH-3X5FK9eH5_Lu1WsaJaNseQNlrSqioyxKmt4XqiCc1oXUGQgWcOApTj8ZLSppcKUUaK4ZpxpIGk4gS7Q9ZQ7OPu51X4UnfFKt63std16keY54QRDAG8nUDnrvdONGJzppNsJwGJvRiglmAAQezMBvzrkbqtO13_wQUUAlhMQJtXaV8Z6ZXRQ8IuGPOmCp1b_RGZTh-kb6zr5ZV1bi1HuWusaF-wZL-i_y3wDfZB_gQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Tao, Weikang</creator><general>Taylor & Francis</general><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></search><sort><creationdate>20051101</creationdate><title>The Mitotic Checkpoint in Cancer Therapy</title><author>Tao, Weikang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-a5f0a3bb9744b7f589c9553d91971a4f4146095573fdac03432c5e454e1262133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Antimitotic Agents - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - physiology</topic><topic>Binding</topic><topic>Biology</topic><topic>Bioscience</topic><topic>Calcium</topic><topic>Cancer</topic><topic>Cell</topic><topic>Cycle</topic><topic>Humans</topic><topic>Landes</topic><topic>Mitosis - drug effects</topic><topic>Mitosis - physiology</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - pathology</topic><topic>Organogenesis</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tao, Weikang</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><jtitle>Cell cycle (Georgetown, Tex.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tao, Weikang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Mitotic Checkpoint in Cancer Therapy</atitle><jtitle>Cell cycle (Georgetown, Tex.)</jtitle><addtitle>Cell Cycle</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>4</volume><issue>11</issue><spage>1495</spage><epage>1499</epage><pages>1495-1499</pages><issn>1538-4101</issn><eissn>1551-4005</eissn><abstract>The mitotic checkpoint is a key cell cycle control mechanism that ensures an accurate segregation of chromosomes during mitosis by delaying the onset of anaphase until all chromosomes are properly attached to a bipolar mitotic spindle. While complete loss of this checkpoint is lethal in vertebrates, a weakened mitotic checkpoint is frequently seen in cancer cells and it may contribute to tumorigenesis. Many antitumor drugs, including spindle assembly inhibitors and DNA damaging agents, can activate the mitotic checkpoint. However, since these drugs influence interphase events besides activating the mitotic checkpoint, the role of the mitotic checkpoint in drug-induced cell death remained unclear. Using a KSP antagonist that specifically acts on mitotic cells, we have recently shown that activation of the mitotic checkpoint followed by mitotic slippage or adaptation, activates Bax and initiates apoptosis. Notably, cells with a weakened mitotic checkpoint incur much less apoptotic death than their checkpoint-proficient counterparts, indicating the requirement of a competent mitotic checkpoint in the induction of apoptosis. 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subjects | Animals Antimitotic Agents - therapeutic use Antineoplastic Agents - therapeutic use Apoptosis - drug effects Apoptosis - physiology Binding Biology Bioscience Calcium Cancer Cell Cycle Humans Landes Mitosis - drug effects Mitosis - physiology Neoplasms - drug therapy Neoplasms - pathology Organogenesis Proteins |
title | The Mitotic Checkpoint in Cancer Therapy |
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