Quantitative gene expression assessment identifies appropriate cell line models for individual cervical cancer pathways

被引:20
作者
Carlson, Mark W.
Iyer, Vishwanath R.
Marcotte, Edward M. [1 ]
机构
[1] Univ Texas, Inst Mol & Cellular Biol, Ctr Syst & Synth Biol, Austin, TX 78712 USA
[2] Univ Texas, Dept Biomed Engn, Austin, TX 78712 USA
关键词
D O I
10.1186/1471-2164-8-117
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Cell lines have been used to study cancer for decades, but truly quantitative assessment of their performance as models is often lacking. We used gene expression profiling to quantitatively assess the gene expression of nine cell line models of cervical cancer. Results: We find a wide variation in the extent to which different cell culture models mimic late-stage invasive cervical cancer biopsies. The lowest agreement was from monolayer HeLa cells, a common cervical cancer model; the highest agreement was from primary epithelial cells, C4-I, and C4-II cell lines. In addition, HeLa and SiHa cell lines cultured in an organotypic environment increased their correlation to cervical cancer significantly. We also find wide variation in agreement when we considered how well individual biological pathways model cervical cancer. Cell lines with an anti-correlation to cervical cancer were also identified and should be avoided. Conclusion: Using gene expression profiling and quantitative analysis, we have characterized nine cell lines with respect to how well they serve as models of cervical cancer. Applying this method to individual pathways, we identified the appropriateness of particular cell lines for studying specific pathways in cervical cancer. This study will allow researchers to choose a cell line with the highest correlation to cervical cancer at a pathway level. This method is applicable to other cancers and could be used to identify the appropriate cell line and growth condition to employ when studying other cancers.
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页数:13
相关论文
共 41 条
[1]   A major constituent of green tea, EGCG, inhibits the growth of a human cervical cancer cell line, CaSki cells, through apoptosis, G1 arrest, and regulation of gene expression [J].
Ahn, WS ;
Huh, SW ;
Bae, SM ;
Lee, IP ;
Lee, JM ;
Namkoong, SE ;
Kim, CK ;
Sin, JI .
DNA AND CELL BIOLOGY, 2003, 22 (03) :217-224
[2]   Singular value decomposition for genome-wide expression data processing and modeling [J].
Alter, O ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) :10101-10106
[3]   The clinicopathologic significance of laminin-5 γ2 chain expression in cervical squamous carcinoma and adenocarcinoma [J].
Andersson, S ;
Hellström, AC ;
Ångström, T ;
Stendahl, U ;
Auer, G ;
Wallin, KL .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2005, 15 (06) :1065-1072
[4]   Two-dimensional gel analysis of protein expression profile in squamous cervical cancer patients [J].
Bae, SM ;
Lee, CH ;
Cho, YL ;
Nam, KH ;
Kim, YW ;
Kim, CK ;
Han, BD ;
Lee, YJ ;
Chun, HJ ;
Ahn, WS .
GYNECOLOGIC ONCOLOGY, 2005, 99 (01) :26-35
[5]   Smad4 deffiency in cervical carcinoma cells [J].
Baldus, SE ;
Schwarz, E ;
Lohrey, C ;
Zapatka, M ;
Landsberg, S ;
Hahn, SA ;
Schmidt, D ;
Dienes, HP ;
Schmiegel, WH ;
Schwarte-Waldhoff, I .
ONCOGENE, 2005, 24 (05) :810-819
[6]   Breast cancer cell lines: friend or foe? [J].
Burdall, SE ;
Hanby, AM ;
Lansdown, MRJ ;
Speirs, V .
BREAST CANCER RESEARCH, 2003, 5 (02) :89-95
[7]   siRNA targeting of the viral E6 oncogene efficiently kills human papillomavirus-positive cancer cells [J].
Butz, K ;
Ristriani, T ;
Hengstermann, A ;
Denk, C ;
Scheffner, M ;
Hoppe-Seyler, F .
ONCOGENE, 2003, 22 (38) :5938-5945
[8]  
Chen Y, 2003, CANCER RES, V63, P1927
[9]   Identification of molecular markers for the early detection of human squamous cell carcinoma of the uterine cervix [J].
Cheng, Q ;
Lau, WM ;
Chew, SH ;
Ho, TH ;
Tay, SK ;
Hui, KM .
BRITISH JOURNAL OF CANCER, 2002, 86 (02) :274-281
[10]  
CHO SG, 2005, CANC LETT