Dexamethasone-induced cisplatin and gemcitabine resistance in lung carcinoma samples treated ex vivo

被引:49
作者
Gassler, N
Zhang, C
Wenger, T
Schnabel, PA
Dienemann, H
Debatin, KM
Mattern, J
Herr, I
机构
[1] German Canc Res Ctr, Clin Cooperat Unit Mol Oncol, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Pathol, D-6900 Heidelberg, Germany
[3] German Canc Res Ctr, Clin Cooperat Unit Nucl Med, D-6900 Heidelberg, Germany
[4] Univ Ulm, Childrens Hosp, D-89069 Ulm, Germany
[5] Univ Heidelberg, Thoraxklin Heidelberg, D-6900 Heidelberg, Germany
关键词
lung cancer; drug resistance; cisplatin; gemcitabine; dexamethasone;
D O I
10.1038/sj.bjc.6602453
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy for lung cancer not only has severe side effects but frequently also exhibits limited, if any clinical effectiveness. Dexamethasone (DEX) and similar glucocorticoids (GCs) such as prednisone are often used in the clinical setting, for example, as cotreatment to prevent nausea and other symptoms. Clinical trials evaluating the impact of GCs on tumour control and patient survival of lung carcinoma have never been performed. Therefore, we isolated cancer cells from resected lung tumour specimens and treated them with cisplatin in the presence or absence of DEX. Cell number of viable and dead cells was evaluated by trypan blue exclusion and viability was measured by the MTT-assay. We found that DEX induced resistance toward cisplatin in all of 10 examined tumour samples. Similar results were found using gemcitabine as cytotoxic drug. Survival of drug-treated lung carcinoma cells in the presence of DEX was longlasting as examined 2 and 3 weeks after cisplatin treatment of a lung carcinoma cell line. These data corroborate recent in vitro and in vivo xenograft findings and rise additional concerns about the widespread combined use of DEX with antineoplastic drugs in the clinical management of patients with lung cancer.
引用
收藏
页码:1084 / 1088
页数:5
相关论文
共 19 条
[1]  
AAPRO MS, 1991, RECENT RES CANCER, V121, P91
[2]   Steroids affect collateral sensitivity to gemcitabine of multidrug-resistant human lung cancer cells [J].
Bergman, AM ;
Pinedo, HM ;
Peters, GJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 416 (1-2) :19-24
[3]   THE PHARMACOKINETICS OF SINGLE HIGH-DOSES OF DEXAMETHASONE IN CANCER-PATIENTS [J].
BRADY, ME ;
SARTIANO, GP ;
ROSENBLUM, SL ;
ZAGLAMA, NE ;
BAUGUESS, CT .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 32 (06) :593-596
[4]  
*CANC RES UK, 2004, STAT PROGN LUNG CANC
[5]   A GFP reporter system to assess gene transfer and expression in human hematopoietic progenitor cells [J].
Cheng, L ;
Du, C ;
Murray, D ;
Tong, X ;
Zhang, YA ;
Chen, BP ;
Hawley, RG .
GENE THERAPY, 1997, 4 (10) :1013-1022
[6]   Recent insights into the mechanism of glucocorticosteroid-induced apoptosis [J].
Distelhorst, CW .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (01) :6-19
[7]  
Herr I, 2003, CANCER RES, V63, P3112
[8]   Dexamethasone for the prophylaxis of radiation-induced emesis: A National Cancer Institute of Canada Clinical Trials Group phase III study [J].
Kirkbride, P ;
Bezjak, A ;
Pater, J ;
Zee, B ;
Palmer, MJ ;
Wong, R ;
Cross, P ;
Gulavita, S ;
Blood, P ;
Sun, A ;
Dundas, G ;
Ganguly, PK ;
Lim, J ;
Chowdhury, AD ;
Kumar, SE ;
Dar, AR .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (09) :1960-1966
[9]  
Kofler R, 2000, HISTOCHEM CELL BIOL, V114, P1
[10]   Cancer mortality in Europe, 1995-1999, and an overview of trends since 1960 [J].
Levi, F ;
Lucchini, F ;
Negri, E ;
Boyle, P ;
La Vecchia, C .
INTERNATIONAL JOURNAL OF CANCER, 2004, 110 (02) :155-169