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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer letters 2013-05, Vol.332 (2), p.359-368
Hauptverfasser: Pore, Milind M, Hiltermann, T. Jeroen N, Kruyt, Frank A.E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 368
container_issue 2
container_start_page 359
container_title Cancer letters
container_volume 332
creator Pore, Milind M
Hiltermann, T. Jeroen N
Kruyt, Frank A.E
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1327725223</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S030438351000457X</els_id><sourcerecordid>3642013481</sourcerecordid><originalsourceid>FETCH-LOGICAL-c469t-2cb946a79dce8d35a92c663d6c38ab54ccc3a75f08b87908d5ba4b106529a1383</originalsourceid><addsrcrecordid>eNqFkc1q3DAUhUVoaaZJ3yA0A90UiqdX_9ImUEL_INBFEsjuIsuaqSYe25Xslnn7anCSQjZdCaTvHh19IuSMwooCVR-3K--6NowrBmUL7AooOyILajSrtDXwgiyAg6i44fKYvM55CwBSaPmKHDOwWkiqF-TDjUubMMZus3RDP4x9jnk5uPHnH7fPy9gt26kclZt8SKfk5dq1Obx5WE_I7ZfPN5ffqqsfX79ffrqqvFB2rJivrVBO28YH03DpLPNK8UZ5blwthfeeOy3XYGqjLZhG1k7UFJRk1tFS94S8n3OH1P-aQh5xF7MPbeu60E8ZKWdaM8kYL-i7Z-i2n1JX2iFVyoBgc6CYKZ_6nFNY45DizqU9UsCDTNziLBMPMhEsFpll7O1D-FTvQvM09GivAOczsHY9uk2KGW-vS4IspjnnmhbiYiZC8fU7hoTZx1BkNjEFP2LTx_91eB7g29hF79r7sA_532sxMwS8Pnz54cdpqSCkvuN_AVmDowI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1668042138</pqid></control><display><type>article</type><title>Targeting apoptosis pathways in lung cancer</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Pore, Milind M ; Hiltermann, T. Jeroen N ; Kruyt, Frank A.E</creator><creatorcontrib>Pore, Milind M ; Hiltermann, T. Jeroen N ; Kruyt, Frank A.E</creatorcontrib><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><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. Jeroen N</creatorcontrib><creatorcontrib>Kruyt, Frank A.E</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pore, Milind M</au><au>Hiltermann, T. Jeroen N</au><au>Kruyt, Frank A.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting apoptosis pathways in lung cancer</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2013-05-28</date><risdate>2013</risdate><volume>332</volume><issue>2</issue><spage>359</spage><epage>368</epage><pages>359-368</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>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.</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>
fulltext fulltext
identifier ISSN: 0304-3835
ispartof Cancer letters, 2013-05, Vol.332 (2), p.359-368
issn 0304-3835
1872-7980
language eng
recordid cdi_proquest_miscellaneous_1327725223
source MEDLINE; Elsevier ScienceDirect Journals Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T03%3A32%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Targeting%20apoptosis%20pathways%20in%20lung%20cancer&rft.jtitle=Cancer%20letters&rft.au=Pore,%20Milind%20M&rft.date=2013-05-28&rft.volume=332&rft.issue=2&rft.spage=359&rft.epage=368&rft.pages=359-368&rft.issn=0304-3835&rft.eissn=1872-7980&rft_id=info:doi/10.1016/j.canlet.2010.09.012&rft_dat=%3Cproquest_cross%3E3642013481%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1668042138&rft_id=info:pmid/20974517&rft_els_id=S030438351000457X&rfr_iscdi=true