Determination of chemotherapeutic activity in vivo by luminescent imaging of luciferase-transfected human tumors

被引:26
作者
Caceres, G
Zankina, R
Zhu, XY
Jiao, JA
Wong, H
Aller, A
Andreotti, P
机构
[1] Rumbaugh Goodwin Inst Canc Res Inc, Plantation, FL 33313 USA
[2] Sunol Mol Corp, Miramar, FL USA
[3] Atlantic Sci Dev Inc, Plantation, FL USA
关键词
imaging; luciferase; topotecan; tumors;
D O I
10.1097/00001813-200308000-00010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human DU-145 prostate and MCF-7 breast tumor cell lines were stably transfected with plasmid pcDNA3.1-Luc expressing firefly luciferase. Studies were performed with the transfected cell lines to evaluate luminescent imaging for measuring the efficacy of anti-cancer agents. In vitro experiments demonstrated a dose response of both cell lines to topotecan (Hycamtin(R)) with an IC50 of 0.013 muM for MCF-7 Luc cells and 0.002 muM for DU-145 Luc cells. In vivo imaging experiments were performed using athymic nude mice inoculated i.p. with 5 x 10(6) MCF-7 cells or s.c. with 5 x 10(6) DU-145 cells and then treated with topotecan at 2.5 mg/kg body weight. Tumor progression and regression were monitored for 27 days. Animals inoculated s.c. with DU-145 Luc cells and then treated with topotecan demonstrated significant tumor growth and regression as measured with calipers and luminescent imaging. High correlation was observed between caliper and imaging results. The correlation coefficient was 0.75 for the control untreated group and 0.93 for the topotecan-treated group. Similarly, tumor progression and regression were measurable using luminescent imaging for untreated and topotecan-treated mice inoculated i.p. with MCF-7 Luc cells. These data indicate that luminescent imaging is a useful tool for evaluating anti-cancer drugs in vivo and may prove to be particularly useful for the development of novel agents. Luminescent imaging could also be used to locate and harvest residual tumors in drug-treated animals in order to study mechanisms of drug resistance. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:569 / 574
页数:6
相关论文
共 54 条
[1]   Camptothecin analogues with enhanced antitumor activity at acidic pH [J].
Adams, DJ ;
Dewhirst, MW ;
Flowers, JL ;
Gamcsik, MP ;
Colvin, OM ;
Manikumar, G ;
Wani, MC ;
Wall, ME .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2000, 46 (04) :263-271
[2]  
Andreotti PE, 2003, RECENT RES CANCER, V161, P3
[3]  
ANDREOTTI PE, 1995, CANCER RES, V55, P5276
[4]  
Bankert R. B., 2000, Immunological Investigations, V29, P171, DOI 10.3109/08820130009062301
[5]   SCID mouse models to study human cancer pathogenesis and approaches to therapy: Potential, limitations, and future directions [J].
Bankert, RB ;
Hess, SD ;
Egilmez, NK .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 :C44-C62
[6]   Elevated tumor lactate concentrations predict for an increased risk of metastases in head-and-neck cancer [J].
Brizel, DM ;
Schroeder, T ;
Scher, RL ;
Walenta, S ;
Clough, RW ;
Dewhirst, MW ;
Mueller-Klieser, W .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (02) :349-353
[7]   Epidermal growth factor receptor expression, signal pathway, and inhibitors in non-small cell lung cancer [J].
Bunn, PA ;
Franklin, W .
SEMINARS IN ONCOLOGY, 2002, 29 (05) :38-44
[8]  
Caceres G, 2002, ANTICANCER RES, V22, P2817
[9]  
CACERES G, 2003, IN PRESS LUMINESCENC
[10]   Organochlorines and breast cancer risk [J].
Calle, EE ;
Frumkin, H ;
Henley, SJ ;
Savitz, DA ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2002, 52 (05) :301-309