Studies on the inhibition of feline EGFR in squamous cell carcinoma Enhancement of radiosensitivity and rescue of resistance to small molecule inhibitors

被引:31
作者
Bergkvist, Gura T. [1 ]
Argyle, David J.
Pang, Lisa Y.
Muirhead, Rhona
Yool, Donald A.
机构
[1] Univ Edinburgh, Royal Dick Sch Vet Studies, Easter Bush Vet Ctr, Roslin, Midlothian, Scotland
关键词
EGFR; squamous cell carcinoma; gefitinib; resistance; RNA interference; animal model; feline; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITOR; UNDERSTANDING RESISTANCE; ACQUIRED-RESISTANCE; RNA INTERFERENCE; LUNG-CANCER; NECK-CANCER; HEAD; CATS; EXPRESSION;
D O I
10.4161/cbt.11.11.15525
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study investigated different methods of EGFR (epithelial growth factor receptor) targeting in feline squamous cell carcinoma with the ultimate aim of establishing a large animal model of human head and neck cancer. Both small molecule receptor tyrosine kinase inhibitor (TKI) and RNA interference (RNAi) techniques were employed to target the feline EGFR. We demonstrated that the human drug gefitinib caused a reduction in cell proliferation and migration in a feline cell line. However, we also document the development of resistance that was not associated with mutation in the kinase domain. RNAi caused a potent reduction in EGFR activity and was able to overcome acquired gefitinib resistance. In addition, RNAi targeting of EGFR, but not gefitinib, caused an additive effect on cell killing when combined with radiation. These results support the use of feline SCC as a model of head and neck cancer in man in the search for novel and effective treatments for both tumors.
引用
收藏
页码:927 / 937
页数:11
相关论文
共 55 条
[1]   ErbB-targeted therapeutic approaches in human cancer [J].
Arteaga, CL .
EXPERIMENTAL CELL RESEARCH, 2003, 284 (01) :122-130
[2]   Novel anticancer targets: revisiting ERBB2 and discovering ERBB3 [J].
Baselga, Jose ;
Swain, Sandra M. .
NATURE REVIEWS CANCER, 2009, 9 (07) :463-475
[3]   Expression of epidermal growth factor receptor (EGFR) and Ki67 in feline oral squamous cell carcinomas (FOSCC) [J].
Bergkvist, G. T. ;
Argyle, D. J. ;
Morrison, L. ;
MacIntyre, N. ;
Hayes, A. ;
Yool, D. A. .
VETERINARY AND COMPARATIVE ONCOLOGY, 2011, 9 (02) :106-117
[4]   Epidermal growth factor receptor as a therapeutic target in veterinary oncology [J].
Bergkvist, G. T. ;
Yool, D. A. .
VETERINARY AND COMPARATIVE ONCOLOGY, 2011, 9 (02) :81-94
[5]  
Bertone ER, 2003, J VET INTERN MED, V17, P557, DOI 10.1892/0891-6640(2003)017<0557:EALRFF>2.3.CO
[6]  
2
[7]   Rapamycin synergizes with the epidermal growth factor receptor inhibitor erlotinib in non-small-cell lung, pancreatic, colon, and breast tumors [J].
Buck, Elizabeth ;
Eyzaguirre, Alexandra ;
Brown, Eric ;
Petti, Filippo ;
McCormack, Siobhan ;
Haley, John D. ;
Iwata, Kenneth K. ;
Gibson, Neil W. ;
Griffin, Graeme .
MOLECULAR CANCER THERAPEUTICS, 2006, 5 (11) :2676-2684
[8]   An alternative approach for investigating the carcinogenicity of indoor air pollution: Pets as sentinels of environmental cancer risk [J].
Bukowski, JA ;
Wartenberg, D .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1997, 105 (12) :1312-1319
[9]   Gαi1 and Gαi3 Are Required for Epidermal Growth Factor-Mediated Activation of the Akt-mTORC1 Pathway [J].
Cao, Cong ;
Huang, Xuesong ;
Han, Yuyuan ;
Wan, Yinsheng ;
Birnbaumer, Lutz ;
Feng, Geng-Sheng ;
Marshall, John ;
Jiang, Meisheng ;
Chu, Wen-Ming .
SCIENCE SIGNALING, 2009, 2 (68) :ra17
[10]   Rapamycin induces transactivation of the EGFR and increases cell survival [J].
Chaturvedi, D. ;
Gao, X. ;
Cohen, M. S. ;
Taunton, J. ;
Patel, T. B. .
ONCOGENE, 2009, 28 (09) :1187-1196