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
[1]   EFFICACY OF ANTIBODIES TO EPIDERMAL GROWTH-FACTOR RECEPTOR AGAINST KB CARCINOMA INVITRO AND IN NUDE-MICE [J].
ABOUDPIRAK, E ;
HURWITZ, E ;
PIRAK, ME ;
BELLOT, F ;
SCHLESSINGER, J ;
SELA, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (20) :1605-1611
[2]  
Alberts Steven R, 2005, Clin Colorectal Cancer, V5, P211, DOI 10.3816/CCC.2005.n.033
[3]   An epidermal growth factor receptor intron 1 polymorphism mediates response to epidermal growth factor receptor inhibitors [J].
Amador, ML ;
Oppenheimer, D ;
Perea, S ;
Maitra, A ;
Cusati, G ;
Iacobuzio-Donahue, C ;
Baker, SD ;
Ashfaq, R ;
Takimoto, C ;
Forastiere, A ;
Hidalgo, M .
CANCER RESEARCH, 2004, 64 (24) :9139-9143
[4]   Effects of pharmacologic antagonists of epidermal growth factor receptor, PI3K and MEK signal kinases on NF-κB and AP-1 activation and IL-8 and VEGF expression in human head and neck squamous cell carcinoma lines [J].
Bancroft, CC ;
Chen, Z ;
Yeh, J ;
Sunwoo, JB ;
Yeh, NT ;
Jackson, S ;
Jackson, C ;
Van Waes, C .
INTERNATIONAL JOURNAL OF CANCER, 2002, 99 (04) :538-548
[5]   Magnetic resonance imaging in an orthotopic rat model: Blockade of epidermal growth factor receptor with EMD72000 inhibits human pancreatic carcinoma growth [J].
Bangard, C ;
Gossmann, A ;
Papyan, A ;
Tawadros, S ;
Hellmich, N ;
Bruns, CJ .
INTERNATIONAL JOURNAL OF CANCER, 2005, 114 (01) :131-138
[6]   ZD1839 ('Iressa')1,2 as an anticancer agent [J].
Baselga, J ;
Averbuch, SD .
DRUGS, 2000, 60 (Suppl 1) :33-40
[7]   Phase I studies of anti-epidermal growth factor receptor chimeric antibody C225 alone and in combination with cisplatin [J].
Baselga, J ;
Pfister, D ;
Cooper, MR ;
Cohen, R ;
Burtness, B ;
Bos, M ;
D'Andrea, G ;
Seidman, A ;
Norton, L ;
Gunnett, K ;
Falcey, J ;
Anderson, V ;
Waksal, H ;
Mendelsohn, J .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (04) :904-914
[8]   Phase II multicenter study of the antiepidermal growth factor receptor monoclonal antibody cetuximab in combination with platinum-based chemotherapy in patients with platinum-refractory metastatic and/or recurrent squamous cell carcinoma of the head and neck [J].
Baselga, J ;
Trigo, JM ;
Bourhis, J ;
Tortochaux, J ;
Cortés-Funes, H ;
Hitt, R ;
Gascón, P ;
Arnellal, N ;
Harstrick, A ;
Eckardt, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5568-5577
[9]   Phase III study of gemcitabine in combination with fluorouracil versus gemcitabine alone in patients with advanced pancreatic carcinoma: Eastern Cooperative Oncology Group Trial E2297 [J].
Berlin, JD ;
Catalano, P ;
Thomas, JP ;
Kugler, JW ;
Haller, DG ;
Benson, AB .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (15) :3270-3275
[10]   Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors [J].
Bianco, R ;
Shin, I ;
Ritter, CA ;
Yakes, FM ;
Basso, A ;
Rosen, N ;
Tsurutani, J ;
Dennis, PA ;
Mills, GB ;
Arteaga, CL .
ONCOGENE, 2003, 22 (18) :2812-2822