Progress towards non-small-cell lung cancer models that represent clinical evolutionary trajectories

被引:40
作者
Hynds, Robert E. [1 ,2 ]
Frese, Kristopher K. [3 ,4 ]
Pearce, David R. [1 ]
Gronroos, Eva [2 ]
Dive, Caroline [3 ,4 ]
Swanton, Charles [1 ,2 ]
机构
[1] UCL, UCL Canc Inst, Canc Res UK Lung Canc Ctr Excellence, London, England
[2] Francis Crick Inst, Canc Evolut & Genome Instabil Lab, London, England
[3] Univ Manchester, Canc Res UK Lung Canc Ctr Excellence, Manchester, Lancs, England
[4] Univ Manchester, Canc Biomarker Ctr, Canc Res UK Manchester Inst, Alderley Pk, Macclesfield, Cheshire, England
基金
英国医学研究理事会; 英国惠康基金; 欧洲研究理事会;
关键词
cell lines; organoids; patient-derived xenografts; genetically engineered mouse models; cancer evolution; model systems; CIRCULATING TUMOR-CELLS; PATIENT-DERIVED XENOGRAFTS; BRONCHIAL EPITHELIAL-CELLS; K-RAS ONCOGENE; IN-VITRO; MOUSE MODELS; T-CELLS; THERAPEUTIC RESPONSES; PRECLINICAL MODEL; DRUG DISCOVERY;
D O I
10.1098/rsob.200247
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:15
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