Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice

Purpose: Non-small cell lung cancers (NSCLC) are a heterogeneous group of carcinomas harboring a variety of different gene mutations. We have utilized two distinct genetically engineered mouse models of human NSCLC (adenocarcinoma) to investigate how genetic factors within tumor parenchymal cells in...

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Main Authors: Perez, Bradford A., Ghafoori, A. Paiman, Lee, Chang-Lung, Johnston, Samuel M., Li, Yifan, Moroshek, Jacob G., Ma, Yan, Mukherjee, Sayan, Kim, Yongbaek, Badea, Cristian T., Kirsch, David G.
Format: Online
Language:English
Published: Frontiers Media S.A. 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613757/
id pubmed-3613757
recordtype oai_dc
spelling pubmed-36137572013-04-05 Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice Perez, Bradford A. Ghafoori, A. Paiman Lee, Chang-Lung Johnston, Samuel M. Li, Yifan Moroshek, Jacob G. Ma, Yan Mukherjee, Sayan Kim, Yongbaek Badea, Cristian T. Kirsch, David G. Oncology Purpose: Non-small cell lung cancers (NSCLC) are a heterogeneous group of carcinomas harboring a variety of different gene mutations. We have utilized two distinct genetically engineered mouse models of human NSCLC (adenocarcinoma) to investigate how genetic factors within tumor parenchymal cells influence the in vivo tumor growth delay after one or two fractions of radiation therapy (RT). Frontiers Media S.A. 2013-04-02 /pmc/articles/PMC3613757/ /pubmed/23565506 http://dx.doi.org/10.3389/fonc.2013.00072 Text en Copyright © 2013 Perez, Ghafoori, Lee, Johnston, Li, Moroshek, Ma, Mukherjee, Kim, Badea and Kirsch. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Perez, Bradford A.
Ghafoori, A. Paiman
Lee, Chang-Lung
Johnston, Samuel M.
Li, Yifan
Moroshek, Jacob G.
Ma, Yan
Mukherjee, Sayan
Kim, Yongbaek
Badea, Cristian T.
Kirsch, David G.
spellingShingle Perez, Bradford A.
Ghafoori, A. Paiman
Lee, Chang-Lung
Johnston, Samuel M.
Li, Yifan
Moroshek, Jacob G.
Ma, Yan
Mukherjee, Sayan
Kim, Yongbaek
Badea, Cristian T.
Kirsch, David G.
Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
author_facet Perez, Bradford A.
Ghafoori, A. Paiman
Lee, Chang-Lung
Johnston, Samuel M.
Li, Yifan
Moroshek, Jacob G.
Ma, Yan
Mukherjee, Sayan
Kim, Yongbaek
Badea, Cristian T.
Kirsch, David G.
author_sort Perez, Bradford A.
title Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
title_short Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
title_full Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
title_fullStr Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
title_full_unstemmed Assessing the Radiation Response of Lung Cancer with Different Gene Mutations Using Genetically Engineered Mice
title_sort assessing the radiation response of lung cancer with different gene mutations using genetically engineered mice
description Purpose: Non-small cell lung cancers (NSCLC) are a heterogeneous group of carcinomas harboring a variety of different gene mutations. We have utilized two distinct genetically engineered mouse models of human NSCLC (adenocarcinoma) to investigate how genetic factors within tumor parenchymal cells influence the in vivo tumor growth delay after one or two fractions of radiation therapy (RT).
publisher Frontiers Media S.A.
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613757/
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