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14-3-3 Proteins Mediate an Essential Anti-apoptotic Signal
The 14-3-3 proteins are a family of highly conserved eukaryotic regulatory molecules that play important roles in many biological processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding and modulating the activity of a host of sig...
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Published in: | The Journal of biological chemistry 2001-11, Vol.276 (48), p.45193-45200 |
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creator | Masters, S C Fu, H |
description | The 14-3-3 proteins are a family of highly conserved eukaryotic regulatory molecules that play important roles in many biological
processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding
and modulating the activity of a host of signaling proteins. The ability of 14-3-3 to inhibit Bad and other proapoptotic proteins
argues that 14-3-3 can support cell survival. To examine this issue in a global sense, a specific inhibitor of 14-3-3/ligand
interactions, difopein, was used. Difopein expression led to induction of apoptosis. Studies using various components of survival
and death signaling pathways were consistent with a vital role for 14-3-3/ligand interactions in signal transduction from
upstream pro-survival kinases to the core apoptotic machinery. Because these kinases often become activated during oncogenesis,
the effect of difopein on cell death induced by antineoplastic drugs was examined. It was found that difopein enhances the
ability of cisplatin to kill cells. These data support the model that 14-3-3, through binding to Bad and other ligands, is
critical for cell survival signaling. Inhibition of 14-3-3 may represent a useful therapeutic target for treatment of cancer
and other diseases involving inappropriate cell survival. |
doi_str_mv | 10.1074/jbc.M105971200 |
format | article |
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processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding
and modulating the activity of a host of signaling proteins. The ability of 14-3-3 to inhibit Bad and other proapoptotic proteins
argues that 14-3-3 can support cell survival. To examine this issue in a global sense, a specific inhibitor of 14-3-3/ligand
interactions, difopein, was used. Difopein expression led to induction of apoptosis. Studies using various components of survival
and death signaling pathways were consistent with a vital role for 14-3-3/ligand interactions in signal transduction from
upstream pro-survival kinases to the core apoptotic machinery. Because these kinases often become activated during oncogenesis,
the effect of difopein on cell death induced by antineoplastic drugs was examined. It was found that difopein enhances the
ability of cisplatin to kill cells. These data support the model that 14-3-3, through binding to Bad and other ligands, is
critical for cell survival signaling. Inhibition of 14-3-3 may represent a useful therapeutic target for treatment of cancer
and other diseases involving inappropriate cell survival.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M105971200</identifier><identifier>PMID: 11577088</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>14-3-3 Proteins ; Amino Acid Sequence ; Animals ; Apoptosis ; Caspase 3 ; Caspases - metabolism ; Cell Death ; Cell Survival ; Cisplatin - pharmacology ; COS Cells ; Dimerization ; Flow Cytometry ; HeLa Cells ; Humans ; Ligands ; Models, Molecular ; Molecular Sequence Data ; Peptides - antagonists & inhibitors ; Peptides - chemistry ; Precipitin Tests ; Protein Binding ; Protein Structure, Tertiary ; Proteins - chemistry ; Proteins - pharmacology ; Signal Transduction ; Time Factors ; Tyrosine 3-Monooxygenase - metabolism ; Tyrosine 3-Monooxygenase - physiology</subject><ispartof>The Journal of biological chemistry, 2001-11, Vol.276 (48), p.45193-45200</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-f5c4fae74238a770455f597ddd6178aed0f7eb516b1ca22d6e79f42c8fef8d4c3</citedby><cites>FETCH-LOGICAL-c405t-f5c4fae74238a770455f597ddd6178aed0f7eb516b1ca22d6e79f42c8fef8d4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11577088$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masters, S C</creatorcontrib><creatorcontrib>Fu, H</creatorcontrib><title>14-3-3 Proteins Mediate an Essential Anti-apoptotic Signal</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The 14-3-3 proteins are a family of highly conserved eukaryotic regulatory molecules that play important roles in many biological
processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding
and modulating the activity of a host of signaling proteins. The ability of 14-3-3 to inhibit Bad and other proapoptotic proteins
argues that 14-3-3 can support cell survival. To examine this issue in a global sense, a specific inhibitor of 14-3-3/ligand
interactions, difopein, was used. Difopein expression led to induction of apoptosis. Studies using various components of survival
and death signaling pathways were consistent with a vital role for 14-3-3/ligand interactions in signal transduction from
upstream pro-survival kinases to the core apoptotic machinery. Because these kinases often become activated during oncogenesis,
the effect of difopein on cell death induced by antineoplastic drugs was examined. It was found that difopein enhances the
ability of cisplatin to kill cells. These data support the model that 14-3-3, through binding to Bad and other ligands, is
critical for cell survival signaling. Inhibition of 14-3-3 may represent a useful therapeutic target for treatment of cancer
and other diseases involving inappropriate cell survival.</description><subject>14-3-3 Proteins</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Caspase 3</subject><subject>Caspases - metabolism</subject><subject>Cell Death</subject><subject>Cell Survival</subject><subject>Cisplatin - pharmacology</subject><subject>COS Cells</subject><subject>Dimerization</subject><subject>Flow Cytometry</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Ligands</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Peptides - antagonists & inhibitors</subject><subject>Peptides - chemistry</subject><subject>Precipitin Tests</subject><subject>Protein Binding</subject><subject>Protein Structure, Tertiary</subject><subject>Proteins - chemistry</subject><subject>Proteins - pharmacology</subject><subject>Signal Transduction</subject><subject>Time Factors</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Tyrosine 3-Monooxygenase - physiology</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEQhoMotlavHmUP4m1rJptsst5KqR_QoqCCt5DNTtqU7W7dbBH_vZEWOpf38sw7w0PINdAxUMnv16UdL4CKQgKj9IQMgaoszQR8nZIhpQzSggk1IBchrGkcXsA5GQAIKalSQ_IAPI188ta1PfomJAusvOkxMU0yCwGb3ps6mcRIzbbd9m3vbfLul42pL8mZM3XAq0OOyOfj7GP6nM5fn16mk3lqORV96oTlzqDkLFMmXuVCuPhuVVU5SGWwok5iKSAvwRrGqhxl4TizyqFTFbfZiNzte7dd-73D0OuNDxbr2jTY7oKWjBVQKBXB8R60XRtCh05vO78x3a8Gqv9t6WhLH23FhZtD867cYHXED3oicLsHVn65-vEd6tK3doUbzWSuudJcQJFlf2TncBM</recordid><startdate>20011130</startdate><enddate>20011130</enddate><creator>Masters, S C</creator><creator>Fu, H</creator><general>American Society for Biochemistry and Molecular Biology</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>20011130</creationdate><title>14-3-3 Proteins Mediate an Essential Anti-apoptotic Signal</title><author>Masters, S C ; Fu, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-f5c4fae74238a770455f597ddd6178aed0f7eb516b1ca22d6e79f42c8fef8d4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>14-3-3 Proteins</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Caspase 3</topic><topic>Caspases - metabolism</topic><topic>Cell Death</topic><topic>Cell Survival</topic><topic>Cisplatin - pharmacology</topic><topic>COS Cells</topic><topic>Dimerization</topic><topic>Flow Cytometry</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Ligands</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Peptides - antagonists & inhibitors</topic><topic>Peptides - chemistry</topic><topic>Precipitin Tests</topic><topic>Protein Binding</topic><topic>Protein Structure, Tertiary</topic><topic>Proteins - chemistry</topic><topic>Proteins - pharmacology</topic><topic>Signal Transduction</topic><topic>Time Factors</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Tyrosine 3-Monooxygenase - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masters, S C</creatorcontrib><creatorcontrib>Fu, H</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>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masters, S C</au><au>Fu, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>14-3-3 Proteins Mediate an Essential Anti-apoptotic Signal</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-11-30</date><risdate>2001</risdate><volume>276</volume><issue>48</issue><spage>45193</spage><epage>45200</epage><pages>45193-45200</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The 14-3-3 proteins are a family of highly conserved eukaryotic regulatory molecules that play important roles in many biological
processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding
and modulating the activity of a host of signaling proteins. The ability of 14-3-3 to inhibit Bad and other proapoptotic proteins
argues that 14-3-3 can support cell survival. To examine this issue in a global sense, a specific inhibitor of 14-3-3/ligand
interactions, difopein, was used. Difopein expression led to induction of apoptosis. Studies using various components of survival
and death signaling pathways were consistent with a vital role for 14-3-3/ligand interactions in signal transduction from
upstream pro-survival kinases to the core apoptotic machinery. Because these kinases often become activated during oncogenesis,
the effect of difopein on cell death induced by antineoplastic drugs was examined. It was found that difopein enhances the
ability of cisplatin to kill cells. These data support the model that 14-3-3, through binding to Bad and other ligands, is
critical for cell survival signaling. Inhibition of 14-3-3 may represent a useful therapeutic target for treatment of cancer
and other diseases involving inappropriate cell survival.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>11577088</pmid><doi>10.1074/jbc.M105971200</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Elsevier ScienceDirect Journals |
subjects | 14-3-3 Proteins Amino Acid Sequence Animals Apoptosis Caspase 3 Caspases - metabolism Cell Death Cell Survival Cisplatin - pharmacology COS Cells Dimerization Flow Cytometry HeLa Cells Humans Ligands Models, Molecular Molecular Sequence Data Peptides - antagonists & inhibitors Peptides - chemistry Precipitin Tests Protein Binding Protein Structure, Tertiary Proteins - chemistry Proteins - pharmacology Signal Transduction Time Factors Tyrosine 3-Monooxygenase - metabolism Tyrosine 3-Monooxygenase - physiology |
title | 14-3-3 Proteins Mediate an Essential Anti-apoptotic Signal |
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