Transforming Growth Factor Alpha Stimulation of Mucosal Tissue Cultures from Head and Neck Squamous Cell Carcinoma Patients Increases Chemoresistance to Cisplatin

被引:4
作者
Baumeister, Philipp [1 ]
Reiter, Maximilian [1 ]
Schwenk-Zieger, Sabina [1 ]
Harreus, Ulrich [1 ]
机构
[1] Univ Munich, Dept Otolaryngol & Head & Neck Surg, DE-81377 Munich, Germany
关键词
Chemoresistance to cisplatin; Transforming growth factor alpha stimulation; Head and neck squamous cell carcinoma; UPPER AERODIGESTIVE TRACT; MINI-ORGAN CULTURES; MULTIDRUG-RESISTANCE; DRUG-RESISTANCE; BREAST-CANCER; EGF-RECEPTOR; TUMOR-CELLS; DNA-DAMAGE; CETUXIMAB; LINES;
D O I
10.1159/000319902
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The monoclonal epidermal growth factor receptor ( EGFR) antibody cetuximab (Erbitux(TM)) was recently approved by the European Medicines Agency for the treatment of recurrent and/or metastatic head and neck squamous cell carcinoma (HNSCC) in combination with a platinum-based chemotherapy. Since the antibody has only a limited effect as a monotherapy, possible explanations for the synergistic effect with cisplatin are enhanced antibody-dependent cytoxicity and increased sensitivity to the drug. Most of our knowledge of EGFR biology in HNSCC is based on studies using EGFR inhibitors and/or antibodies. Our study was designed to evaluate the impact of EGFR stimulation on cisplatin-induced DNA damage. Therefore, tissue cultures were produced of tumor-free oropharyngeal mucosa biopsies of HNSCC patients and controls. In a previous study, overexpression of EGFR in tissue cultures from tumor patients compared to controls was confirmed by immunohistochemical staining. Twenty-four-hour stimulation of tissue cultures with transforming growth factor alpha (TGF-alpha), a specific EGFR ligand, resulted in a reduction of cisplatin-induced DNA damage by 35% in cases, whereas in controls TGF-alpha had no effect. This reflects a statistically significant increase in cellular chemoresistance to cisplatin following TGF-alpha stimulation and helps to further understand effects of EGFR antisense therapy in combination with chemotherapy. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:268 / 274
页数:7
相关论文
共 42 条
[1]   Antiproliferative effects of rapamycin as a single agent and in combination with carboplatin and paclitaxel in head and neck cancer cell lines [J].
Aissat, Nasredine ;
Le Tourneau, Christophe ;
Ghoul, Aida ;
Serova, Maria ;
Bieche, Ivan ;
Lokiec, Francois ;
Raymond, Eric ;
Faivre, Sandrine .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2008, 62 (02) :305-313
[2]  
Ang KK, 2002, CANCER RES, V62, P7350
[3]   Transforming Growth Factor-alpha reduces carcinogen-induced DNA damage in mini-organ cultures from head-and-neck cancer patients [J].
Baumeister, Philipp ;
Schwenk-Zieger, Sabina ;
Reiter, Maximilian ;
Welz, Christian ;
Harreus, Ulrich .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2009, 677 (1-2) :42-45
[4]   Cetuximab in the treatment of head and neck cancer [J].
Bernier, Jacques .
EXPERT REVIEW OF ANTICANCER THERAPY, 2006, 6 (11) :1539-1552
[5]  
Blasiak J, 2000, TERATOGEN CARCIN MUT, V20, P119, DOI 10.1002/(SICI)1520-6866(2000)20:3<119::AID-TCM3>3.0.CO
[6]  
2-Z
[7]  
Bonner JA, 2000, J CLIN ONCOL, V18, p47S
[8]  
Bos M, 1997, CLIN CANCER RES, V3, P2099
[9]   The EGF/ErbB receptor family and apoptosis [J].
Danielsen, AJ ;
Maihle, NJ .
GROWTH FACTORS, 2002, 20 (01) :1-15
[10]   EGF induces cell motility and multi-drug resistance gene expression in breast cancer cells [J].
Garcia, Ruben ;
Franklin, Richard A. ;
McCubrey, James A. .
CELL CYCLE, 2006, 5 (23) :2820-2826