Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories
Non-small-cell lung cancer (NSCLC) is the leading cause of cancer-related deaths worldwide. Although advances are being made towards earlier detection and the development of impactful targeted therapies and immunotherapies, the 5-year survival of patients with advanced disease is still below 20%. Ef...
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Online Access: | https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200247 |
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doaj-726d0207c380411f80bae211ade2e7432021-03-15T15:51:14ZengThe Royal SocietyOpen Biology2046-24412021-01-0111110.1098/rsob.200247200247Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectoriesRobert E. HyndsKristopher K. FreseDavid R. PearceEva GrönroosCaroline DiveCharles SwantonNon-small-cell lung cancer (NSCLC) is the leading cause of cancer-related deaths worldwide. Although advances are being made towards earlier detection and the development of impactful targeted therapies and immunotherapies, the 5-year survival of patients with advanced disease is still below 20%. Effective cancer research relies on pre-clinical model systems that accurately reflect the evolutionary course of disease progression and mimic patient responses to therapy. Here, we review pre-clinical models, including genetically engineered mouse models and patient-derived materials, such as cell lines, primary cell cultures, explant cultures and xenografts, that are currently being used to interrogate NSCLC evolution from pre-invasive disease through locally invasive cancer to the metastatic colonization of distant organ sites.https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200247cell linesorganoidspatient-derived xenograftsgenetically engineered mouse modelscancer evolutionmodel systems |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Robert E. Hynds Kristopher K. Frese David R. Pearce Eva Grönroos Caroline Dive Charles Swanton |
spellingShingle |
Robert E. Hynds Kristopher K. Frese David R. Pearce Eva Grönroos Caroline Dive Charles Swanton Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories Open Biology cell lines organoids patient-derived xenografts genetically engineered mouse models cancer evolution model systems |
author_facet |
Robert E. Hynds Kristopher K. Frese David R. Pearce Eva Grönroos Caroline Dive Charles Swanton |
author_sort |
Robert E. Hynds |
title |
Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
title_short |
Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
title_full |
Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
title_fullStr |
Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
title_full_unstemmed |
Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
title_sort |
progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories |
publisher |
The Royal Society |
series |
Open Biology |
issn |
2046-2441 |
publishDate |
2021-01-01 |
description |
Non-small-cell lung cancer (NSCLC) is the leading cause of cancer-related deaths worldwide. Although advances are being made towards earlier detection and the development of impactful targeted therapies and immunotherapies, the 5-year survival of patients with advanced disease is still below 20%. Effective cancer research relies on pre-clinical model systems that accurately reflect the evolutionary course of disease progression and mimic patient responses to therapy. Here, we review pre-clinical models, including genetically engineered mouse models and patient-derived materials, such as cell lines, primary cell cultures, explant cultures and xenografts, that are currently being used to interrogate NSCLC evolution from pre-invasive disease through locally invasive cancer to the metastatic colonization of distant organ sites. |
topic |
cell lines organoids patient-derived xenografts genetically engineered mouse models cancer evolution model systems |
url |
https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200247 |
work_keys_str_mv |
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