Therapeutic targeting of receptor tyrosine kinases in lung cancer
Lung cancer is a difficult illness with a poor overall survival. Even though combination strategies with chemotherapy, radiation therapy and surgery have all been utilised, the overall outcome for this disease continues to be relatively disappointing. In order to make a difference in the treatment o...
Gespeichert in:
Veröffentlicht in: | Expert opinion on therapeutic targets 2005-06, Vol.9 (3), p.533-559 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 559 |
---|---|
container_issue | 3 |
container_start_page | 533 |
container_title | Expert opinion on therapeutic targets |
container_volume | 9 |
creator | Choong, Nicholas W Ma, Patrick C Salgia, Ravi |
description | Lung cancer is a difficult illness with a poor overall survival. Even though combination strategies with chemotherapy, radiation therapy and surgery have all been utilised, the overall outcome for this disease continues to be relatively disappointing. In order to make a difference in the treatment of lung cancer, novel therapeutics will have to be developed. Through basic biological studies, a number of receptor tyrosine kinases have been implicated in the pathogenesis and progression of lung cancer. In this review, the authors summarise the mechanisms of several major receptor tyrosine kinases in lung cancer, especially epidermal growth factor receptor, Her2/neu, MET, vascular endothelial growth factor and KIT. The biology associated with these receptors is described, and the various novel therapeutic inhibitory strategies that are ongoing in preclinical and clinical studies for lung cancer are detailed. Through understanding of receptor tyrosine kinases and the utilisation of specific inhibitors, it is hopeful that a dramatic impact will be made on the biology and therapy for lung cancer. |
doi_str_mv | 10.1517/14728222.9.3.533 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_67922177</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67922177</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-6e0a67f07c17da8cd5cc702b9c3914337ebabab67c62b2bc0f58f391131e12523</originalsourceid><addsrcrecordid>eNp9kM9LwzAUx4Mobk7vnqQnb6350TatnmT4CwZe5jmk6euW2TY1SZH992ZsIh6Ud3gPvj94fBC6JDghGeE3JOW0oJQmZcKSjLEjNCU8TWOeM3Ic7iDHO32CzpzbYExxmeWnaEKyMi1yTqfofrkGKwcYvVaRl3YFXveryDSRBQWDNzbyW2uc7iF617104CLdR-0YTEr2Cuw5Omlk6-DisGfo7fFhOX-OF69PL_P7RaxSjH2cA5Y5bzBXhNeyUHWmFMe0KhUrScoYh0qGybnKaUUrhZusaIJEGAFCM8pm6HrfO1jzMYLzotNOQdvKHszoRM5LSgnnwYj3RhX-dhYaMVjdSbsVBIsdNvGNTZSCiYAtRK4O3WPVQf0TOHAKhru9QfeNsZ38NLathZfb1tjGBg7aCfZP_e2v9Bpk69dKWhAbM9o-YPv7ty8QcI4k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67922177</pqid></control><display><type>article</type><title>Therapeutic targeting of receptor tyrosine kinases in lung cancer</title><source>MEDLINE</source><source>Taylor & Francis Medical Library - CRKN</source><source>Taylor & Francis Journals Complete</source><creator>Choong, Nicholas W ; Ma, Patrick C ; Salgia, Ravi</creator><creatorcontrib>Choong, Nicholas W ; Ma, Patrick C ; Salgia, Ravi</creatorcontrib><description>Lung cancer is a difficult illness with a poor overall survival. Even though combination strategies with chemotherapy, radiation therapy and surgery have all been utilised, the overall outcome for this disease continues to be relatively disappointing. In order to make a difference in the treatment of lung cancer, novel therapeutics will have to be developed. Through basic biological studies, a number of receptor tyrosine kinases have been implicated in the pathogenesis and progression of lung cancer. In this review, the authors summarise the mechanisms of several major receptor tyrosine kinases in lung cancer, especially epidermal growth factor receptor, Her2/neu, MET, vascular endothelial growth factor and KIT. The biology associated with these receptors is described, and the various novel therapeutic inhibitory strategies that are ongoing in preclinical and clinical studies for lung cancer are detailed. Through understanding of receptor tyrosine kinases and the utilisation of specific inhibitors, it is hopeful that a dramatic impact will be made on the biology and therapy for lung cancer.</description><identifier>ISSN: 1472-8222</identifier><identifier>EISSN: 1744-7631</identifier><identifier>DOI: 10.1517/14728222.9.3.533</identifier><identifier>PMID: 15948672</identifier><language>eng</language><publisher>England: Ashley Publications Ltd</publisher><subject>Antibodies, Monoclonal - pharmacology ; Antibodies, Monoclonal - therapeutic use ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; epidermal growth factor receptor (EGFR) ; Humans ; lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - enzymology ; Receptor Protein-Tyrosine Kinases - antagonists & inhibitors ; Receptor Protein-Tyrosine Kinases - metabolism ; receptor tyrosine kinase</subject><ispartof>Expert opinion on therapeutic targets, 2005-06, Vol.9 (3), p.533-559</ispartof><rights>Ashley Publications Ltd 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-6e0a67f07c17da8cd5cc702b9c3914337ebabab67c62b2bc0f58f391131e12523</citedby><cites>FETCH-LOGICAL-c400t-6e0a67f07c17da8cd5cc702b9c3914337ebabab67c62b2bc0f58f391131e12523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1517/14728222.9.3.533$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1517/14728222.9.3.533$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,59620,59726,60409,60515</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15948672$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choong, Nicholas W</creatorcontrib><creatorcontrib>Ma, Patrick C</creatorcontrib><creatorcontrib>Salgia, Ravi</creatorcontrib><title>Therapeutic targeting of receptor tyrosine kinases in lung cancer</title><title>Expert opinion on therapeutic targets</title><addtitle>Expert Opin Ther Targets</addtitle><description>Lung cancer is a difficult illness with a poor overall survival. Even though combination strategies with chemotherapy, radiation therapy and surgery have all been utilised, the overall outcome for this disease continues to be relatively disappointing. In order to make a difference in the treatment of lung cancer, novel therapeutics will have to be developed. Through basic biological studies, a number of receptor tyrosine kinases have been implicated in the pathogenesis and progression of lung cancer. In this review, the authors summarise the mechanisms of several major receptor tyrosine kinases in lung cancer, especially epidermal growth factor receptor, Her2/neu, MET, vascular endothelial growth factor and KIT. The biology associated with these receptors is described, and the various novel therapeutic inhibitory strategies that are ongoing in preclinical and clinical studies for lung cancer are detailed. Through understanding of receptor tyrosine kinases and the utilisation of specific inhibitors, it is hopeful that a dramatic impact will be made on the biology and therapy for lung cancer.</description><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>epidermal growth factor receptor (EGFR)</subject><subject>Humans</subject><subject>lung cancer</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - enzymology</subject><subject>Receptor Protein-Tyrosine Kinases - antagonists & inhibitors</subject><subject>Receptor Protein-Tyrosine Kinases - metabolism</subject><subject>receptor tyrosine kinase</subject><issn>1472-8222</issn><issn>1744-7631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9LwzAUx4Mobk7vnqQnb6350TatnmT4CwZe5jmk6euW2TY1SZH992ZsIh6Ud3gPvj94fBC6JDghGeE3JOW0oJQmZcKSjLEjNCU8TWOeM3Ic7iDHO32CzpzbYExxmeWnaEKyMi1yTqfofrkGKwcYvVaRl3YFXveryDSRBQWDNzbyW2uc7iF617104CLdR-0YTEr2Cuw5Omlk6-DisGfo7fFhOX-OF69PL_P7RaxSjH2cA5Y5bzBXhNeyUHWmFMe0KhUrScoYh0qGybnKaUUrhZusaIJEGAFCM8pm6HrfO1jzMYLzotNOQdvKHszoRM5LSgnnwYj3RhX-dhYaMVjdSbsVBIsdNvGNTZSCiYAtRK4O3WPVQf0TOHAKhru9QfeNsZ38NLathZfb1tjGBg7aCfZP_e2v9Bpk69dKWhAbM9o-YPv7ty8QcI4k</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Choong, Nicholas W</creator><creator>Ma, Patrick C</creator><creator>Salgia, Ravi</creator><general>Ashley Publications Ltd</general><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>20050601</creationdate><title>Therapeutic targeting of receptor tyrosine kinases in lung cancer</title><author>Choong, Nicholas W ; Ma, Patrick C ; Salgia, Ravi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-6e0a67f07c17da8cd5cc702b9c3914337ebabab67c62b2bc0f58f391131e12523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>epidermal growth factor receptor (EGFR)</topic><topic>Humans</topic><topic>lung cancer</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - enzymology</topic><topic>Receptor Protein-Tyrosine Kinases - antagonists & inhibitors</topic><topic>Receptor Protein-Tyrosine Kinases - metabolism</topic><topic>receptor tyrosine kinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choong, Nicholas W</creatorcontrib><creatorcontrib>Ma, Patrick C</creatorcontrib><creatorcontrib>Salgia, Ravi</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>Expert opinion on therapeutic targets</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choong, Nicholas W</au><au>Ma, Patrick C</au><au>Salgia, Ravi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Therapeutic targeting of receptor tyrosine kinases in lung cancer</atitle><jtitle>Expert opinion on therapeutic targets</jtitle><addtitle>Expert Opin Ther Targets</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>9</volume><issue>3</issue><spage>533</spage><epage>559</epage><pages>533-559</pages><issn>1472-8222</issn><eissn>1744-7631</eissn><abstract>Lung cancer is a difficult illness with a poor overall survival. Even though combination strategies with chemotherapy, radiation therapy and surgery have all been utilised, the overall outcome for this disease continues to be relatively disappointing. In order to make a difference in the treatment of lung cancer, novel therapeutics will have to be developed. Through basic biological studies, a number of receptor tyrosine kinases have been implicated in the pathogenesis and progression of lung cancer. In this review, the authors summarise the mechanisms of several major receptor tyrosine kinases in lung cancer, especially epidermal growth factor receptor, Her2/neu, MET, vascular endothelial growth factor and KIT. The biology associated with these receptors is described, and the various novel therapeutic inhibitory strategies that are ongoing in preclinical and clinical studies for lung cancer are detailed. Through understanding of receptor tyrosine kinases and the utilisation of specific inhibitors, it is hopeful that a dramatic impact will be made on the biology and therapy for lung cancer.</abstract><cop>England</cop><pub>Ashley Publications Ltd</pub><pmid>15948672</pmid><doi>10.1517/14728222.9.3.533</doi><tpages>27</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1472-8222 |
ispartof | Expert opinion on therapeutic targets, 2005-06, Vol.9 (3), p.533-559 |
issn | 1472-8222 1744-7631 |
language | eng |
recordid | cdi_proquest_miscellaneous_67922177 |
source | MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete |
subjects | Antibodies, Monoclonal - pharmacology Antibodies, Monoclonal - therapeutic use Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use epidermal growth factor receptor (EGFR) Humans lung cancer Lung Neoplasms - drug therapy Lung Neoplasms - enzymology Receptor Protein-Tyrosine Kinases - antagonists & inhibitors Receptor Protein-Tyrosine Kinases - metabolism receptor tyrosine kinase |
title | Therapeutic targeting of receptor tyrosine kinases 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=2025-02-21T20%3A13%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Therapeutic%20targeting%20of%20receptor%20tyrosine%20kinases%20in%20lung%20cancer&rft.jtitle=Expert%20opinion%20on%20therapeutic%20targets&rft.au=Choong,%20Nicholas%20W&rft.date=2005-06-01&rft.volume=9&rft.issue=3&rft.spage=533&rft.epage=559&rft.pages=533-559&rft.issn=1472-8222&rft.eissn=1744-7631&rft_id=info:doi/10.1517/14728222.9.3.533&rft_dat=%3Cproquest_pubme%3E67922177%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67922177&rft_id=info:pmid/15948672&rfr_iscdi=true |