Lung cancer cell lines: Useless artifacts or invaluable tools for medical science?

被引:100
作者
Gazdar, Adi F. [1 ]
Gao, Boning [1 ]
Minna, John D. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
关键词
Lung cancer; Cell lines; Preneoplasia; Oncogenes; Tumor suppressor genes; Genetic instability; GROWTH-FACTOR RECEPTOR; BRONCHIAL EPITHELIAL-CELLS; TUMOR-SUPPRESSOR LOCUS; CLINICAL-RESPONSE; RADIATION SENSITIZATION; EPIGENETIC INACTIVATION; MALIGNANT PHENOTYPE; KINASE DOMAIN; MUTATIONS; EGFR;
D O I
10.1016/j.lungcan.2009.12.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple cell lines (estimated at 300-400) have been established from human small cell (SCLC) and non-small cell lung cancers (NSCLC). These cell lines have been widely dispersed to and used by the scientific community worldwide, with over 8000 citations resulting from their study. However, there remains considerable skepticism on the part of the scientific community as to the validity of research resulting from their use. These questions center around the genomic instability of cultured cells, lack of differentiation of cultured cells and absence of stromal-vascular-inflammatory cell compartments. In this report we discuss the advantages and disadvantages of the use of cell lines, address the issues of instability and lack of differentiation. Perhaps the most important finding is that every important, recurrent genetic and epigenetic change including gene mutations, deletions, amplifications, translocations and methylation-induced gene silencing found in tumors has been identified in cell lines and vice versa. These "driver mutations" represented in cell lines offer opportunities for biological characterization and application to translational research. Another potential shortcoming of cell lines is the difficulty of studying multistage pathogenesis in vitro. To overcome this problem, we have developed cultures from central and peripheral airways that serve as models for the multistage pathogenesis of tumors arising in these two very different compartments. Finally the issue of cell line contamination must be addressed and safeguarded against. A full understanding of the advantages and shortcomings of cell lines is required for the investigator to derive the maximum benefit from their use. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:309 / 318
页数:10
相关论文
共 97 条
[61]   Gene expression profiling of cancer stem cell in human lung adenocarcinoma A549 cells [J].
Seo, Dong-Cheol ;
Sung, Ji-Min ;
Cho, Hee-Jung ;
Yi, Hee ;
Seo, Kun-Ho ;
Choi, In-Soo ;
Kim, Dong-Ku ;
Kim, Jin-Suk ;
Am, Abd El-Aty ;
Shin, Ho-Chul .
MOLECULAR CANCER, 2007, 6 (1)
[62]   A genome-wide screen for promoter methylation in lung cancer identifies novel methylation markers for multiple malignancies [J].
Shames, David S. ;
Girard, Luc ;
Gao, Boning ;
Sato, Mitsuo ;
Lewis, Cheryl M. ;
Shivapurkar, Narayan ;
Jiang, Aixiang ;
Perou, Charles M. ;
Kim, Young H. ;
Pollack, Jonathan R. ;
Fong, Kwun M. ;
Lam, Chi-Leung ;
Wong, Maria ;
Shyr, Yu ;
Nanda, Rita ;
Olopade, Olufunmilayo I. ;
Gerald, William ;
Euhus, David M. ;
Shay, Jerry W. ;
Gazdar, Adi F. ;
Minna, John D. .
PLOS MEDICINE, 2006, 3 (12) :2244-2263
[63]   DNA methylation in health, disease, and cancer [J].
Shames, David S. ;
Minna, John D. ;
Gazdar, Adi F. .
CURRENT MOLECULAR MEDICINE, 2007, 7 (01) :85-102
[64]   Epidermal growth factor receptor mutations in lung cancer [J].
Sharma, Sreenath V. ;
Bell, Daphne W. ;
Settleman, Jeffrey ;
Haber, Daniel A. .
NATURE REVIEWS CANCER, 2007, 7 (03) :169-181
[65]   Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers [J].
Shigematsu, H ;
Lin, L ;
Takahashi, T ;
Nomura, M ;
Suzuki, M ;
Wistuba, II ;
Fong, KM ;
Lee, H ;
Toyooka, S ;
Shimizu, N ;
Fujisawa, T ;
Feng, ZD ;
Roth, JA ;
Herz, J ;
Minna, JD ;
Gazdar, AF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (05) :339-346
[66]   Loss of expression of death-inducing signaling complex (DISC) components in lung cancer cell lines and the influence of MYC amplification [J].
Shivapurkar, N ;
Reddy, J ;
Matta, H ;
Sathyanarayana, UG ;
Huang, CX ;
Toyooka, S ;
Minna, JD ;
Chaudhary, PM ;
Gazdar, AF .
ONCOGENE, 2002, 21 (55) :8510-8514
[67]   Differential inactivation of caspase-8 in lung cancers [J].
Shivapurkar, N ;
Toyooka, S ;
Eby, MT ;
Huang, CX ;
Sathyanarayana, UG ;
Cunningham, HT ;
Reddy, JL ;
Brambilla, E ;
Takahashi, J ;
Minna, JD ;
Choudhary, PM ;
Gazdar, AF .
CANCER BIOLOGY & THERAPY, 2002, 1 (01) :65-69
[68]   A Gene Expression Signature Associated with "K-Ras Addiction" Reveals Regulators of EMT and Tumor Cell Survival [J].
Singh, Anurag ;
Greninger, Patricia ;
Rhodes, Daniel ;
Koopman, Louise ;
Violette, Sheila ;
Bardeesy, Nabeel ;
Settleman, Jeff .
CANCER CELL, 2009, 15 (06) :489-500
[69]  
SLEBOS RJC, 1989, EUR RESPIR J, V2, P461
[70]   Oncogene Mutations, Copy Number Gains and Mutant Allele Specific Imbalance (MASI) Frequently Occur Together in Tumor Cells [J].
Soh, Junichi ;
Okumura, Naoki ;
Lockwood, William W. ;
Yamamoto, Hiromasa ;
Shigematsu, Hisayuki ;
Zhang, Wei ;
Chari, Raj ;
Shames, David S. ;
Tang, Ximing ;
MacAulay, Calum ;
Varella-Garcia, Marileila ;
Vooder, Tonu ;
Wistuba, Ignacio I. ;
Lam, Stephen ;
Brekken, Rolf ;
Toyooka, Shinichi ;
Minna, John D. ;
Lam, Wan L. ;
Gazdar, Adi F. .
PLOS ONE, 2009, 4 (10)