Tumorgrafts as In Vivo Surrogates for Women with Ovarian Cancer

被引:156
作者
Weroha, S. John [1 ]
Becker, Marc A. [1 ]
Enderica-Gonzalez, Sergio [1 ]
Harrington, Sean C. [1 ]
Oberg, Ann L. [4 ]
Maurer, Matthew J. [4 ]
Perkins, Sarah E. [4 ]
AlHilli, Mariam [5 ]
Butler, Kristina A. [5 ]
McKinstry, Sarah [1 ]
Fink, Stephanie [6 ]
Jenkins, Robert B. [6 ]
Hou, Xiaonan [1 ]
Kalli, Kimberly R. [1 ]
Goodman, Karin M. [1 ]
Sarkaria, Jann N. [2 ]
Karlan, Beth Y. [7 ]
Kumar, Amanika [5 ]
Kaufmann, Scott H. [1 ,3 ]
Hartmann, Lynn C. [1 ]
Haluska, Paul [1 ]
机构
[1] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[5] Mayo Clin, Div Gynecol Surg, Rochester, MN 55905 USA
[6] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[7] Cedars Sinai Med Ctr, Samuel Oschin Canc Inst, Womens Canc Program, Los Angeles, CA 90048 USA
关键词
PRIMARY PERITONEAL; CELL-LINES; XENOGRAFTS; CARCINOMA; MOUSE; MICE; INTRAPERITONEAL; NORMALIZATION; ESTABLISHMENT; CARBOPLATIN;
D O I
10.1158/1078-0432.CCR-13-2611
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Ovarian cancer has a high recurrence and mortality rate. A barrier to improved outcomes includes a lack of accurate models for preclinical testing of novel therapeutics. Experimental Design: Clinically relevant, patient-derived tumorgraft models were generated from sequential patients and the first 168 engrafted models are described. Fresh ovarian, primary, peritoneal, and fallopian tube carcinomas were collected at the time of debulking surgery and injected intraperitoneally into severe combined immunodeficient mice. Results: Tumorgrafts demonstrated a 74% engraftment rate with microscopic fidelity of primary tumor characteristics. Low-passage tumorgrafts also showed comparable genomic aberrations with the corresponding primary tumor and exhibit gene set enrichment of multiple ovarian cancer molecular subtypes, similar to patient tumors. Importantly, each of these tumorgraft models is annotated with clinical data and for those that have been tested, response to platinum chemotherapy correlates with the source patient. Conclusions: Presented herein is the largest known living tumor bank of patient-derived, ovarian tumorgraft models that can be applied to the development of personalized cancer treatment. (C) 2014 AACR.
引用
收藏
页码:1288 / 1297
页数:10
相关论文
共 41 条
[1]  
[Anonymous], 2009, SEER Cancer Statistics Review, 1975-2006
[2]   Humanized Mouse Model of Ovarian Cancer Recapitulates Patient Solid Tumor Progression, Ascites Formation, and Metastasis [J].
Bankert, Richard B. ;
Balu-Iyer, Sathy V. ;
Odunsi, Kunle ;
Shultz, Leonard D. ;
Kelleher, Raymond J., Jr. ;
Barnas, Jennifer L. ;
Simpson-Abelson, Michelle ;
Parsons, Robert ;
Yokota, Sandra J. .
PLOS ONE, 2011, 6 (09)
[3]   Comparison between primary peritoneal and epithelial ovarian carcinoma: A polpulation-based study [J].
Barda, G ;
Menczer, J ;
Chetrit, A ;
Lubin, F ;
Beck, D ;
Piura, B ;
Glezerman, M ;
Modan, B ;
Sadetzki, S .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2004, 190 (04) :1039-1045
[4]   Ovarian cancer: Changes in patterns at diagnosis and relative survival over the last three decades [J].
Barnholtz-Sloan, JS ;
Schwartz, AG ;
Qureshi, F ;
Jacques, S ;
Malone, J ;
Munkarah, AR .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2003, 189 (04) :1120-1127
[5]   Integrated genomic analyses of ovarian carcinoma [J].
Bell, D. ;
Berchuck, A. ;
Birrer, M. ;
Chien, J. ;
Cramer, D. W. ;
Dao, F. ;
Dhir, R. ;
DiSaia, P. ;
Gabra, H. ;
Glenn, P. ;
Godwin, A. K. ;
Gross, J. ;
Hartmann, L. ;
Huang, M. ;
Huntsman, D. G. ;
Iacocca, M. ;
Imielinski, M. ;
Kalloger, S. ;
Karlan, B. Y. ;
Levine, D. A. ;
Mills, G. B. ;
Morrison, C. ;
Mutch, D. ;
Olvera, N. ;
Orsulic, S. ;
Park, K. ;
Petrelli, N. ;
Rabeno, B. ;
Rader, J. S. ;
Sikic, B. I. ;
Smith-McCune, K. ;
Sood, A. K. ;
Bowtell, D. ;
Penny, R. ;
Testa, J. R. ;
Chang, K. ;
Dinh, H. H. ;
Drummond, J. A. ;
Fowler, G. ;
Gunaratne, P. ;
Hawes, A. C. ;
Kovar, C. L. ;
Lewis, L. R. ;
Morgan, M. B. ;
Newsham, I. F. ;
Santibanez, J. ;
Reid, J. G. ;
Trevino, L. R. ;
Wu, Y. -Q. ;
Wang, M. .
NATURE, 2011, 474 (7353) :609-615
[6]   SPECIES-SPECIFIC RECOGNITION PATTERNS OF MONOCLONAL-ANTIBODIES DIRECTED AGAINST VIMENTIN [J].
BOHN, W ;
WIEGERS, W ;
BEUTTENMULLER, M ;
TRAUB, P .
EXPERIMENTAL CELL RESEARCH, 1992, 201 (01) :1-7
[7]   Construction and Characterization of Novel, Recombinant Immunotoxins Targeting the Her2/neu Oncogene Product: In vitro and In vivo Studies [J].
Cao, Yu ;
Marks, James D. ;
Marks, John W. ;
Cheung, Lawrence H. ;
Kim, Sehoon ;
Rosenblum, Michael G. .
CANCER RESEARCH, 2009, 69 (23) :8987-8995
[8]   p16-Cdk4-Rb axis controls sensitivity to a cyclin-dependent kinase inhibitor PD0332991 in glioblastoma xenograft cells [J].
Cen, Ling ;
Carlson, Brett L. ;
Schroeder, Mark A. ;
Ostrem, Jamie L. ;
Kitange, Gaspar J. ;
Mladek, Ann C. ;
Fink, Stephanie R. ;
Decker, Paul A. ;
Wu, Wenting ;
Kim, Jung-Sik ;
Waldman, Todd ;
Jenkins, Robert B. ;
Sarkaria, Jann N. .
NEURO-ONCOLOGY, 2012, 14 (07) :870-881
[9]  
CUSTER RP, 1985, AM J PATHOL, V120, P464
[10]   Evaluating cell lines as tumour models by comparison of genomic profiles [J].
Domcke, Silvia ;
Sinha, Rileen ;
Levine, Douglas A. ;
Sander, Chris ;
Schultz, Nikolaus .
NATURE COMMUNICATIONS, 2013, 4