A Brain Tumor/Organotypic Slice Co-culture System for Studying Tumor Microenvironment and Targeted Drug Therapies

被引:25
作者
Chadwick, Emily J. [1 ]
Yang, David P. [1 ]
Filbin, Mariella G. [2 ]
Mazzola, Emanuele [3 ]
Sun, Yu [1 ]
Behar, Oded [1 ,4 ]
Pazyra-Murphy, Maria F. [1 ]
Goumnerova, Liliana [5 ]
Ligon, Keith L. [6 ]
Stiles, Charles D. [1 ]
Segal, Rosalind A. [1 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[2] Childrens Hosp, Dept Pediat, Boston, MA 02215 USA
[3] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02215 USA
[4] Hebrew Univ Jerusalem, Dept Dev Biol & Canc Res, IL-91905 Jerusalem, Israel
[5] Childrens Hosp, Dept Neurosurg, Boston, MA 02215 USA
[6] Dana Farber Canc Inst, Dept Med Oncol, Ctr Mol Oncol Pathol, Boston, MA 02215 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2015年 / 105期
关键词
Medicine; Issue; 105; Tumor; Brain; Microenvironment; Treatment; Mouse; Astrocytoma; Slice; Co-Culture; CELLS;
D O I
10.3791/53304
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Brain tumors are a major cause of cancer-related morbidity and mortality. Developing new therapeutics for these cancers is difficult, as many of these tumors are not easily grown in standard culture conditions. Neurosphere cultures under serum-free conditions and orthotopic xenografts have expanded the range of tumors that can be maintained. However, many types of brain tumors remain difficult to propagate or study. This is particularly true for pediatric brain tumors such as pilocytic astrocytomas and medulloblastomas. This protocol describes a system that allows primary human brain tumors to be grown in culture. This quantitative assay can be used to investigate the effect of microenvironment on tumor growth, and to test new drug therapies. This protocol describes a system where fluorescently labeled brain tumor cells are grown on an organotypic brain slice from a juvenile mouse. The response of tumor cells to drug treatments can be studied in this assay, by analyzing changes in the number of cells on the slice over time. In addition, this system can address the nature of the microenvironment that normally fosters growth of brain tumors. This brain tumor organotypic slice co-culture assay provides a propitious system for testing new drugs on human tumor cells within a brain microenvironment.
引用
收藏
页数:13
相关论文
共 11 条
[1]   Interfering with Resistance to Smoothened Antagonists by Inhibition of the PI3K Pathway in Medulloblastoma [J].
Buonamici, Silvia ;
Williams, Juliet ;
Morrissey, Michael ;
Wang, Anlai ;
Guo, Ribo ;
Vattay, Anthony ;
Hsiao, Kathy ;
Yuan, Jing ;
Green, John ;
Ospina, Beatriz ;
Yu, Qunyan ;
Ostrom, Lance ;
Fordjour, Paul ;
Anderson, Dustin L. ;
Monahan, John E. ;
Kelleher, Joseph F. ;
Peukert, Stefan ;
Pan, Shifeng ;
Wu, Xu ;
Maira, Sauveur-Michel ;
Garcia-Echeverria, Carlos ;
Briggs, Kimberly J. ;
Watkins, D. Neil ;
Yao, Yung-mae ;
Lengauer, Christoph ;
Warmuth, Markus ;
Sellers, William R. ;
Dorsch, Marion .
SCIENCE TRANSLATIONAL MEDICINE, 2010, 2 (51)
[2]   Proteoglycan interactions with Sonic Hedgehog specify mitogenic responses [J].
Chan, Jennifer A. ;
Balasubramanian, Srividya ;
Witt, Rochelle M. ;
Nazemi, Kellie J. ;
Choi, Yoojin ;
Pazyra-Murphy, Maria F. ;
Walsh, Carolyn O. ;
Thompson, Margaret ;
Segal, Rosalind A. .
NATURE NEUROSCIENCE, 2009, 12 (04) :409-417
[3]   Migration from a mitogenic niche promotes cell-cycle exit [J].
Choi, Y ;
Borghesani, PR ;
Chan, JA ;
Segal, RA .
JOURNAL OF NEUROSCIENCE, 2005, 25 (45) :10437-10445
[4]   Manifestations of pilocytic astrocytoma: A pictorial review [J].
Chourmouzi D. ;
Papadopoulou E. ;
Konstantinidis M. ;
Syrris V. ;
Kouskouras K. ;
Haritanti A. ;
Karkavelas G. ;
Drevelegas A. .
Insights into Imaging, 2014, 5 (3) :387-402
[5]   Preferential brain locations of low-grade gliomas [J].
Duffau, H ;
Capelle, L .
CANCER, 2004, 100 (12) :2622-2626
[6]  
Heddleston J.M., 2013, CURR PHARM DESIGN, V17, P2386
[7]   Quantitative high throughput screening using a primary human three-dimensional organotypic culture predicts in vivo efficacy [J].
Kenny, Hilary A. ;
Lal-Nag, Madhu ;
White, Erin A. ;
Shen, Min ;
Chiang, Chun-Yi ;
Mitra, Anirban K. ;
Zhang, Yilin ;
Curtis, Marion ;
Schryver, Elizabeth M. ;
Bettis, Sam ;
Jadhav, Ajit ;
Boxer, Matthew B. ;
Li, Zhuyin ;
Ferrer, Marc ;
Lengyel, Ernst .
NATURE COMMUNICATIONS, 2015, 6
[8]   ROCK Inhibitor and Feeder Cells Induce the Conditional Reprogramming of Epithelial Cells [J].
Liu, Xuefeng ;
Ory, Virginie ;
Chapman, Sandra ;
Yuan, Hang ;
Albanese, Chris ;
Kallakury, Bhaskar ;
Timofeeva, Olga A. ;
Nealon, Caitlin ;
Dakic, Aleksandra ;
Simic, Vera ;
Haddad, Bassem R. ;
Rhim, Johng S. ;
Dritschilo, Anatoly ;
Riegel, Anna ;
McBride, Alison ;
Schlegel, Richard .
AMERICAN JOURNAL OF PATHOLOGY, 2012, 180 (02) :599-607
[9]   The 2007 WHO classification of tumours of the central nervous system (vol 114, pg 97, 2007) [J].
Louis, David N. ;
Ohgaki, Hiroko ;
Wiestler, Otmar D. ;
Cavenee, Webster K. ;
Burger, Peter C. ;
Jouvet, Anne ;
Scheithauer, Bernd W. ;
Kleihues, Paul .
ACTA NEUROPATHOLOGICA, 2007, 114 (05) :547-547
[10]   Shh pathway activity is down-regulated in cultured medulloblastoma cells: Implications for preclinical studies [J].
Sasai, K ;
Romer, JT ;
Lee, Y ;
Finkelstein, D ;
Fuller, C ;
McKinnon, PJ ;
Curran, T .
CANCER RESEARCH, 2006, 66 (08) :4215-4222