Epidermal growth factor receptor-targeted therapy for pancreatic cancer

被引:24
作者
Papageorgio, Chris [1 ]
Perry, Michael C. [1 ]
机构
[1] Univ Missouri, Ellis Fischel Canc Ctr, Columbia, MO 65203 USA
关键词
targeted therapy; epidermal growth factor; tyrosine kinase; angiogenesis;
D O I
10.1080/07357900701522653
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical and experimental work supports the view that the epidermal growth factor receptor (EGFR) is a relevant target for cancer therapy. Expression of EGFR is exaggerated in pancreatic adenocarcinoma and activation of EGFR appears to have an important role in the growth and differentiation of this and other types of cancers. EGFR-targeted therapeutic approaches have shown clinical activity in advanced human cancers for which chemotherapy over the last 30 years has sustained a mere palliative role at best. Therefore, the need remains for novel anticancer therapies that effectively and specifically target epithelial tumor cells while minimizing the toxic side-effects commonly associated with cytotoxic conventional therapies. Agents capable of inhibiting EGFR activity with resultant inhibition of cell proliferation and angiogenesis have significant potential as chemotherapeutic agents for the treatment of pancreatic adenocarcinomas as well as multiple other malignancies.
引用
收藏
页码:647 / 657
页数:11
相关论文
共 155 条
[51]   Requirement of Stat3 but not Stat1 activation for epidermal growth factor receptor-mediated cell growth in vitro [J].
Grandis, JR ;
Drenning, SD ;
Chakraborty, A ;
Zhou, MY ;
Zeng, Q ;
Tweardy, DJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1385-1392
[52]   A multispecialty approach to the diagnosis and management of pancreatic cancer [J].
Hawes, RH ;
Xiong, QH ;
Waxman, I ;
Chang, KJ ;
Evans, DB ;
Abbruzzese, JL .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2000, 95 (01) :17-31
[53]   DIMERIZATION OF CELL-SURFACE RECEPTORS IN SIGNAL-TRANSDUCTION [J].
HELDIN, CH .
CELL, 1995, 80 (02) :213-223
[54]   Mechanism of action and in vivo role of platelet-derived growth factor [J].
Heldin, CH ;
Westermark, B .
PHYSIOLOGICAL REVIEWS, 1999, 79 (04) :1283-1316
[55]   Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: A phase III trial - INTACT 2 [J].
Herbst, RS ;
Giaccone, G ;
Schiller, JH ;
Natale, RB ;
Miller, V .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :785-794
[56]   Phase II multicenter study of the epidermal growth factor receptor antibody cetuximab and cisplatin for recurrent and refractory squamous cell carcinoma of the head and neck [J].
Herbst, RS ;
Arquette, M ;
Shin, DM ;
Dicke, K ;
Vokes, EE ;
Azarnia, N ;
Hong, WK ;
Kies, MS .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5578-5587
[57]   Monoclonal antibodies to target epidermal growth factor receptor-positive tumors - A new paradigm for cancer therapy [J].
Herbst, RS ;
Shin, DM .
CANCER, 2002, 94 (05) :1593-1611
[58]   Phase I and pharmacologic study of OSI-774, an epidermal growth factor receptor tyrosine kinase inhibitor, in patients with advanced solid malignancies [J].
Hidalgo, M ;
Siu, LL ;
Nemunaitis, J ;
Rizzo, J ;
Hammond, LA ;
Takimoto, C ;
Eckhardt, SG ;
Tolcher, A ;
Britten, CD ;
Denis, L ;
Ferrante, K ;
Von Hoff, DD ;
Silberman, S ;
Rowinsky, EK .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (13) :3267-3279
[59]   Protein tyrosine kinase structure and function [J].
Hubbard, SR ;
Till, JH .
ANNUAL REVIEW OF BIOCHEMISTRY, 2000, 69 :373-398
[60]   Juxtamembrane autoinhibition in receptor tyrosine kinases [J].
Hubbard, SR .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (06) :464-470