Method for Novel Anti-Cancer Drug Development using Tumor Explants of Surgical Specimens

被引:5
作者
Joshi, Kaushal [1 ]
Demir, Habibe [1 ]
Yamada, Ryosuke [1 ]
Miyazaki, Takeshi [1 ]
Ray-Chaudhury, Abhik [2 ]
Nakano, Ichiro [1 ]
机构
[1] Ohio State Univ, Med Ctr, Dept Neurol Surg, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Dept Pathol, Columbus, OH 43210 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2011年 / 53期
关键词
Medicine; Issue; 53; Glioblastoma multiforme; glioma; temozolomide; therapeutics; drug design;
D O I
10.3791/2846
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
The current therapies for malignant glioma have only palliative effect. For therapeutic development, one hurdle is the discrepancy of efficacy determined by current drug efficacy tests and the efficacy on patients. Thus, novel and reliable methods for evaluating drug efficacy are warranted in pre-clinical phase. In vitro culture of tumor tissues, including cell lines, has substantial phenotypic, genetic, and epigenetic alterations of cancer cells caused by artificial environment of cell culture, which may not reflect the biology of original tumors in situ. Xenograft models with the immunodeficient mice also have limitations, i.e., the lack of immune system and interspecies genetic and epigenetic discrepancies in microenvironment. Here, we demonstrate a novel method using the surgical specimens of malignant glioma as undissociated tumor blocks to evaluate treatment effects. To validate this method, data with the current first-line chemotherapeutic agent, temozolomide (TMZ), are described. We used the freshly-removed surgical specimen of malignant glioma for our experiments. We performed intratumoral injection of TMZ or other drug candidates, followed by incubation and analysis on surgical specimens. Here, we sought to establish a tumor tissue explant method as a platform to determine the efficacy of novel anti-cancer therapies so that we may be able to overcome, at least, some of the current limitations and fill the existing gap between the current experimental data and the efficacy on an actual patient's tumor. This method may have the potential to accelerate identifying novel chemotherapeutic agents for solid cancer treatment.
引用
收藏
页数:5
相关论文
共 10 条
[1]   Tumor invasion after treatment of glioblastoma with bevacizumab: radiographic and pathologic correlation in humans and mice [J].
de Groot, John F. ;
Fuller, Gregory ;
Kumar, Ashok J. ;
Piao, Yuji ;
Eterovic, Karina ;
Ji, Yongjie ;
Conrad, Charles A. .
NEURO-ONCOLOGY, 2010, 12 (03) :233-242
[2]  
He J., 2010, J PROTEOME RES
[3]  
Heimberger AB, 2000, CLIN CANCER RES, V6, P4148
[4]   Cancerous stem cells can arise from pediatric brain tumors [J].
Hemmati, HD ;
Nakano, I ;
Lazareff, JA ;
Masterman-Smith, M ;
Geschwind, DH ;
Bronner-Fraser, M ;
Kornblum, HI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :15178-15183
[5]   Inhibition of Notch Signaling in Glioblastoma Targets Cancer Stem Cells via an Endothelial Cell Intermediate [J].
Hovinga, Koos E. ;
Shimizu, Fumiko ;
Wang, Rong ;
Panagiotakos, Georgia ;
Van Der Heijden, Maartje ;
Moayedpardazi, Hamideh ;
Correia, Ana Sofia ;
Soulet, Denis ;
Major, Tamara ;
Menon, Jayanthi ;
Tabar, Viviane .
STEM CELLS, 2010, 28 (06) :1019-1029
[6]   Neurosphere Formation Is an Independent Predictor of Clinical Outcome in Malignant Glioma [J].
Laks, Dan R. ;
Masterman-Smith, Michael ;
Visnyei, Koppany ;
Angenieux, Brigitte ;
Orozco, Nicholas M. ;
Foran, Ian ;
Yong, William H. ;
Vinters, Harry V. ;
Liau, Linda M. ;
Lazareff, Jorge A. ;
Mischel, Paul S. ;
Cloughesy, Timothy F. ;
Horvath, Steve ;
Kornblum, Harley I. .
STEM CELLS, 2009, 27 (04) :980-987
[7]  
Ma Yue-hui, 2008, Chinese Journal of Pathology, V37, P333
[8]   Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells [J].
Nakano, Ichiro ;
Masterman-Smith, Michael ;
Saigusa, Kuniyasu ;
Paucar, Andres A. ;
Horvath, Steve ;
Shoemaker, Lorelei ;
Watanabe, Momoko ;
Negro, Alejandra ;
Bajpai, Ruchi ;
Howes, Amy ;
Lelievre, Vincent ;
Waschek, James A. ;
Lazareff, Jorge A. ;
Freije, William A. ;
Liau, Linda M. ;
Gilbertson, Richard J. ;
Cloughesy, Timothy F. ;
Geschwind, Daniel H. ;
Nelson, Stanley F. ;
Mischel, Paul S. ;
Terskikh, Alexey V. ;
Kornblum, Harley I. .
JOURNAL OF NEUROSCIENCE RESEARCH, 2008, 86 (01) :48-60
[9]   Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis [J].
Phillips, HS ;
Kharbanda, S ;
Chen, RH ;
Forrest, WF ;
Soriano, RH ;
Wu, TD ;
Misra, A ;
Nigro, JM ;
Colman, H ;
Soroceanu, L ;
Williams, PM ;
Modrusan, Z ;
Feuerstein, BG ;
Aldape, K .
CANCER CELL, 2006, 9 (03) :157-173
[10]   Brain tumor stem cells maintain overall phenotype and tumorigenicity after in vitro culturing in serum-free conditions [J].
Vik-Mo, Einar Osland ;
Sandberg, Cecilie ;
Olstorn, Havard ;
Varghese, Mercy ;
Brandal, Petter ;
Ramm-Pettersen, Jon ;
Murrell, Wayne ;
Langmoen, Iver Arne .
NEURO-ONCOLOGY, 2010, 12 (12) :1220-1230