Suicide gene therapy on spontaneous canine melanoma: correlations between in vivo tumors and their derived multicell spheroids in vitro

被引:20
作者
Gil-Cardeza, M. L. [1 ]
Villaverde, M. S. [1 ]
Fiszman, G. L. [1 ]
Altamirano, N. A. [1 ]
Cwirenbaum, R. A. [1 ]
Glikin, G. C. [1 ]
Finocchiaro, L. M. E. [1 ]
机构
[1] Univ Buenos Aires, Inst Oncol Angel H Roffo, Unidad Transferencia Genet, RA-1417 Buenos Aires, DF, Argentina
关键词
spheroids; HSV thymidine kinase; melanoma; lipofection; DMRIE; multicellular resistance; EXPRESSION; VIMENTIN; CELLS;
D O I
10.1038/gt.2009.107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To validate the use of multicellular spheroids to predict the efficacy of herpes simplex thymidine kinase/ganciclovir (HSVtk/GCV) suicide gene therapy in the respective in vivo tumors, we established and characterized 15 melanoma-derived cell lines from surgically excised melanoma tumors. Three HSVtk-lipofected cell lines were not sensitive to GCV in any culture configuration, other five displayed similar sensitivity as monolayers or spheroids, and only one resulted more sensitive when grown as spheroids. Other six cell lines manifested a relative multicellular resistance (MCR) phenotype growing as spheroids, compared with the same cells growing as monolayers. The reverse correlation between the MCR and the monolayers survival to HSVtk/GCV suggests that one of the main causes of MCR would be the rapid cell repopulation after suicide gene treatment. The high correlation of MCR with the spheroids radial growth and with the mitotic index of the respective originary tumors supported this re-growth involvement. A remarkable finding was the high correlation in HSVtk/GCV sensitivity between in vivo tumor and the corresponding derived cell lines growing as spheroids (R-2 = 0.85). This strongly encourages the implementation of spheroids as highly realistic experimental model for optimizing and predicting the in vivo response of the respective tumors to therapeutic strategies. Gene Therapy (2010) 17, 26-36; doi: 10.1038/gt.2009.107; published online 10 September 2009
引用
收藏
页码:26 / 36
页数:11
相关论文
共 22 条
[1]  
ALTAMIRANO NA, 2007, CANC DRUG RESISTANCE, P119
[2]  
Brown JM, 1998, CANCER RES, V58, P1408
[3]  
Casais CC, 2006, GENE THER MOL BIOL, V10B, P207
[4]   Multicellular resistance: a paradigm for clinical resistance? [J].
Desoize, B ;
Jardillier, JC .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2000, 36 (2-3) :193-207
[5]  
FELGNER JH, 1994, J BIOL CHEM, V269, P2550
[6]   Suicide gene and cytokines combined nonviral gene therapy for spontaneous canine melanoma [J].
Finocchiaro, L. M. E. ;
Fiszman, G. L. ;
Karara, A. L. ;
Glikin, G. C. .
CANCER GENE THERAPY, 2008, 15 (03) :165-172
[7]   Cytokine-enhanced vaccine and suicide gene therapy as surgery adjuvant treatments for spontaneous canine melanoma [J].
Finocchiaro, L. M. E. ;
Glikin, G. C. .
GENE THERAPY, 2008, 15 (04) :267-276
[8]   Herpes simplex virus thymidine kinase/ganciclovir system in multicellular tumor spheroids [J].
Finocchiaro, LME ;
Bumaschny, VF ;
Karara, AL ;
Fiszman, GL ;
Casais, CC ;
Glikin, GC .
CANCER GENE THERAPY, 2004, 11 (05) :333-345
[9]  
Gao X, 1995, GENE THER, V2, P710
[10]   COEXPRESSION OF VIMENTIN AND KERATINS BY HUMAN-MELANOMA TUMOR-CELLS - CORRELATION WITH INVASIVE AND METASTATIC POTENTIAL [J].
HENDRIX, MJC ;
SEFTOR, EA ;
CHU, YW ;
SEFTOR, REB ;
NAGLE, RB ;
MCDANIEL, KM ;
LEONG, SPL ;
YOHEM, KH ;
LEIBOVITZ, AM ;
MEYSKENS, FL ;
CONAWAY, DH ;
WELCH, DR ;
LIOTTA, LA ;
STETLERSTEVENSON, W .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (03) :165-174