HSP90 as a novel molecular target in non-small-cell lung cancer

Khashayar Esfahani, Victor Cohen Segal Cancer Center, Jewish General Hospital, McGill University, Montreal, QC, Canada Abstract: Lung cancer remains the most lethal cancer, with over 160,000 annual deaths in the USA alone. Over the past decade, the discovery of driver mutations has changed the land...

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Autores principales: Esfahani K, Cohen V
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2016
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Acceso en línea:https://doaj.org/article/c825e459e0d84d2aafce3734f4eeb073
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spelling oai:doaj.org-article:c825e459e0d84d2aafce3734f4eeb0732021-12-02T03:03:03ZHSP90 as a novel molecular target in non-small-cell lung cancer1179-2728https://doaj.org/article/c825e459e0d84d2aafce3734f4eeb0732016-03-01T00:00:00Zhttps://www.dovepress.com/hsp90-as-a-novel-molecular-target-in-non-small-cell-lung-cancer-peer-reviewed-article-LCTThttps://doaj.org/toc/1179-2728Khashayar Esfahani, Victor Cohen Segal Cancer Center, Jewish General Hospital, McGill University, Montreal, QC, Canada Abstract: Lung cancer remains the most lethal cancer, with over 160,000 annual deaths in the USA alone. Over the past decade, the discovery of driver mutations has changed the landscape for the treatment of non-small-cell lung cancer (NSCLC). Targeted therapies against epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) have now been approved by the Food and Drug Administration as part of the standard first-line treatment of NSCLC. Despite good initial responses, most patients develop resistance within 8–12 months and have disease progression. Keywords: non-small-cell lung cancer, driver mutations, targeted therapy, heat shock protein 90 (HSP90)Esfahani KCohen VDove Medical PressarticleNon-small cell lung cancerdriver mutationstargeted therapyheat shock protein 90 (HSP90)Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENLung Cancer: Targets and Therapy, Vol 2016, Iss Issue 1, Pp 11-17 (2016)
institution DOAJ
collection DOAJ
language EN
topic Non-small cell lung cancer
driver mutations
targeted therapy
heat shock protein 90 (HSP90)
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Non-small cell lung cancer
driver mutations
targeted therapy
heat shock protein 90 (HSP90)
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Esfahani K
Cohen V
HSP90 as a novel molecular target in non-small-cell lung cancer
description Khashayar Esfahani, Victor Cohen Segal Cancer Center, Jewish General Hospital, McGill University, Montreal, QC, Canada Abstract: Lung cancer remains the most lethal cancer, with over 160,000 annual deaths in the USA alone. Over the past decade, the discovery of driver mutations has changed the landscape for the treatment of non-small-cell lung cancer (NSCLC). Targeted therapies against epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) have now been approved by the Food and Drug Administration as part of the standard first-line treatment of NSCLC. Despite good initial responses, most patients develop resistance within 8–12 months and have disease progression. Keywords: non-small-cell lung cancer, driver mutations, targeted therapy, heat shock protein 90 (HSP90)
format article
author Esfahani K
Cohen V
author_facet Esfahani K
Cohen V
author_sort Esfahani K
title HSP90 as a novel molecular target in non-small-cell lung cancer
title_short HSP90 as a novel molecular target in non-small-cell lung cancer
title_full HSP90 as a novel molecular target in non-small-cell lung cancer
title_fullStr HSP90 as a novel molecular target in non-small-cell lung cancer
title_full_unstemmed HSP90 as a novel molecular target in non-small-cell lung cancer
title_sort hsp90 as a novel molecular target in non-small-cell lung cancer
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/c825e459e0d84d2aafce3734f4eeb073
work_keys_str_mv AT esfahanik hsp90asanovelmoleculartargetinnonsmallcelllungcancer
AT cohenv hsp90asanovelmoleculartargetinnonsmallcelllungcancer
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