Targeting apoptosis pathways in lung cancer
Lung cancer is a devastating disease with a poor prognosis. Non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) represent different forms of lung cancer that are associated with distinct genetic causes and display different responses to therapy in the clinic. Whereas SCLC is often s...
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Veröffentlicht in: | Cancer letters 2013-05, Vol.332 (2), p.359-368 |
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description | Lung cancer is a devastating disease with a poor prognosis. Non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) represent different forms of lung cancer that are associated with distinct genetic causes and display different responses to therapy in the clinic. Whereas SCLC is often sensitive to chemotherapy at start of treatment, NSCLC are less chemo-sensitive. In NSCLC different histological subtypes are distinguished and increasing efforts are made to identify subtypes that respond to specific therapies, such as those harbouring epidermal growth factor receptor (EGFR) mutations that have benefit from treatment with EGFR inhibitors. Targeting of the apoptotic machinery represents another approach that aims to selectively kill cancer cells while sparing normal ones. Here we describe different ways that are currently explored to induce apoptosis in lung cancer cells, specifically pathways controlled by TNF-related apoptosis-inducing ligand (TRAIL), BCL-2 family members and apoptosis inhibitory proteins (IAPs). Preclinical studies are discussed and for some agents results from early clinical studies and future perspectives are considered. |
doi_str_mv | 10.1016/j.canlet.2010.09.012 |
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Here we describe different ways that are currently explored to induce apoptosis in lung cancer cells, specifically pathways controlled by TNF-related apoptosis-inducing ligand (TRAIL), BCL-2 family members and apoptosis inhibitory proteins (IAPs). Preclinical studies are discussed and for some agents results from early clinical studies and future perspectives are considered.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2010.09.012</identifier><identifier>PMID: 20974517</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Antineoplastic Agents - therapeutic use ; Apoptosis ; BCL-2 ; Cancer therapies ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - pathology ; chemotherapy ; clinical trials ; Cytochrome ; Cytotoxicity ; epidermal growth factor receptors ; Hematology, Oncology and Palliative Medicine ; Humans ; Inhibitor of Apoptosis Proteins - metabolism ; Lung cancer ; lung neoplasms ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Medical prognosis ; Mutation ; Polycyclic aromatic hydrocarbons ; prognosis ; Proteins ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; Receptor, Epidermal Growth Factor - genetics ; Rodents ; Small Cell Lung Carcinoma - drug therapy ; Small Cell Lung Carcinoma - pathology ; Survivin ; Therapy ; TNF-Related Apoptosis-Inducing Ligand - metabolism ; TRAIL ; Tumors ; X-Linked Inhibitor of Apoptosis Protein - metabolism ; XIAP</subject><ispartof>Cancer letters, 2013-05, Vol.332 (2), p.359-368</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2010 Elsevier Ireland Ltd</rights><rights>Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited May 28, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-2cb946a79dce8d35a92c663d6c38ab54ccc3a75f08b87908d5ba4b106529a1383</citedby><cites>FETCH-LOGICAL-c469t-2cb946a79dce8d35a92c663d6c38ab54ccc3a75f08b87908d5ba4b106529a1383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.canlet.2010.09.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20974517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pore, Milind M</creatorcontrib><creatorcontrib>Hiltermann, T. Jeroen N</creatorcontrib><creatorcontrib>Kruyt, Frank A.E</creatorcontrib><title>Targeting apoptosis pathways in lung cancer</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Lung cancer is a devastating disease with a poor prognosis. Non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) represent different forms of lung cancer that are associated with distinct genetic causes and display different responses to therapy in the clinic. Whereas SCLC is often sensitive to chemotherapy at start of treatment, NSCLC are less chemo-sensitive. In NSCLC different histological subtypes are distinguished and increasing efforts are made to identify subtypes that respond to specific therapies, such as those harbouring epidermal growth factor receptor (EGFR) mutations that have benefit from treatment with EGFR inhibitors. Targeting of the apoptotic machinery represents another approach that aims to selectively kill cancer cells while sparing normal ones. Here we describe different ways that are currently explored to induce apoptosis in lung cancer cells, specifically pathways controlled by TNF-related apoptosis-inducing ligand (TRAIL), BCL-2 family members and apoptosis inhibitory proteins (IAPs). Preclinical studies are discussed and for some agents results from early clinical studies and future perspectives are considered.</description><subject>Animals</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Apoptosis</subject><subject>BCL-2</subject><subject>Cancer therapies</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>chemotherapy</subject><subject>clinical trials</subject><subject>Cytochrome</subject><subject>Cytotoxicity</subject><subject>epidermal growth factor receptors</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Inhibitor of Apoptosis Proteins - metabolism</subject><subject>Lung cancer</subject><subject>lung neoplasms</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical prognosis</subject><subject>Mutation</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>prognosis</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>Receptor, Epidermal Growth Factor - genetics</subject><subject>Rodents</subject><subject>Small Cell Lung Carcinoma - drug therapy</subject><subject>Small Cell Lung Carcinoma - pathology</subject><subject>Survivin</subject><subject>Therapy</subject><subject>TNF-Related Apoptosis-Inducing Ligand - metabolism</subject><subject>TRAIL</subject><subject>Tumors</subject><subject>X-Linked Inhibitor of Apoptosis Protein - metabolism</subject><subject>XIAP</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1q3DAUhUVoaaZJ3yA0A90UiqdX_9ImUEL_INBFEsjuIsuaqSYe25Xslnn7anCSQjZdCaTvHh19IuSMwooCVR-3K--6NowrBmUL7AooOyILajSrtDXwgiyAg6i44fKYvM55CwBSaPmKHDOwWkiqF-TDjUubMMZus3RDP4x9jnk5uPHnH7fPy9gt26kclZt8SKfk5dq1Obx5WE_I7ZfPN5ffqqsfX79ffrqqvFB2rJivrVBO28YH03DpLPNK8UZ5blwthfeeOy3XYGqjLZhG1k7UFJRk1tFS94S8n3OH1P-aQh5xF7MPbeu60E8ZKWdaM8kYL-i7Z-i2n1JX2iFVyoBgc6CYKZ_6nFNY45DizqU9UsCDTNziLBMPMhEsFpll7O1D-FTvQvM09GivAOczsHY9uk2KGW-vS4IspjnnmhbiYiZC8fU7hoTZx1BkNjEFP2LTx_91eB7g29hF79r7sA_532sxMwS8Pnz54cdpqSCkvuN_AVmDowI</recordid><startdate>20130528</startdate><enddate>20130528</enddate><creator>Pore, Milind M</creator><creator>Hiltermann, T. Jeroen N</creator><creator>Kruyt, Frank A.E</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Limited</general><scope>FBQ</scope><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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20130528</creationdate><title>Targeting apoptosis pathways in lung cancer</title><author>Pore, Milind M ; Hiltermann, T. Jeroen N ; Kruyt, Frank A.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-2cb946a79dce8d35a92c663d6c38ab54ccc3a75f08b87908d5ba4b106529a1383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Apoptosis</topic><topic>BCL-2</topic><topic>Cancer therapies</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>chemotherapy</topic><topic>clinical trials</topic><topic>Cytochrome</topic><topic>Cytotoxicity</topic><topic>epidermal growth factor receptors</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Inhibitor of Apoptosis Proteins - metabolism</topic><topic>Lung cancer</topic><topic>lung neoplasms</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical prognosis</topic><topic>Mutation</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>prognosis</topic><topic>Proteins</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><topic>Receptor, Epidermal Growth Factor - genetics</topic><topic>Rodents</topic><topic>Small Cell Lung Carcinoma - drug therapy</topic><topic>Small Cell Lung Carcinoma - pathology</topic><topic>Survivin</topic><topic>Therapy</topic><topic>TNF-Related Apoptosis-Inducing Ligand - metabolism</topic><topic>TRAIL</topic><topic>Tumors</topic><topic>X-Linked Inhibitor of Apoptosis Protein - metabolism</topic><topic>XIAP</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pore, Milind M</creatorcontrib><creatorcontrib>Hiltermann, T. 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In NSCLC different histological subtypes are distinguished and increasing efforts are made to identify subtypes that respond to specific therapies, such as those harbouring epidermal growth factor receptor (EGFR) mutations that have benefit from treatment with EGFR inhibitors. Targeting of the apoptotic machinery represents another approach that aims to selectively kill cancer cells while sparing normal ones. Here we describe different ways that are currently explored to induce apoptosis in lung cancer cells, specifically pathways controlled by TNF-related apoptosis-inducing ligand (TRAIL), BCL-2 family members and apoptosis inhibitory proteins (IAPs). Preclinical studies are discussed and for some agents results from early clinical studies and future perspectives are considered.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>20974517</pmid><doi>10.1016/j.canlet.2010.09.012</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents - therapeutic use Apoptosis BCL-2 Cancer therapies Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - pathology chemotherapy clinical trials Cytochrome Cytotoxicity epidermal growth factor receptors Hematology, Oncology and Palliative Medicine Humans Inhibitor of Apoptosis Proteins - metabolism Lung cancer lung neoplasms Lung Neoplasms - drug therapy Lung Neoplasms - pathology Medical prognosis Mutation Polycyclic aromatic hydrocarbons prognosis Proteins Proto-Oncogene Proteins c-bcl-2 - metabolism Receptor, Epidermal Growth Factor - genetics Rodents Small Cell Lung Carcinoma - drug therapy Small Cell Lung Carcinoma - pathology Survivin Therapy TNF-Related Apoptosis-Inducing Ligand - metabolism TRAIL Tumors X-Linked Inhibitor of Apoptosis Protein - metabolism XIAP |
title | Targeting apoptosis pathways in lung cancer |
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