The type III epidermal growth factor receptor mutation - Biological significance and potential target for anti-cancer therapy

被引:197
作者
Pedersen, MW [1 ]
Meltorn, M [1 ]
Damstrup, L [1 ]
Poulsen, HS [1 ]
机构
[1] Natl Univ Hosp, Dept Radiat Biol, Finsen Ctr, Sect 6321, DK-2100 Copenhagen, Denmark
关键词
cancer; EGFRvIII; function; therapy;
D O I
10.1023/A:1011177318162
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations in the epidermal growth factor receptor occur frequently in a number of human tumours including gliomas, non-small-cell lung carcinomas, ovarian carcinomas and prostate carcinomas. The type III epidermal growth factor receptor mutation (variously named EGFRvIII, de2-7 EGFR or Delta EGFR), which lacks a portion of the extracellular ligand binding domain, is the most common. Here, we review the current status with regard to the role of EGFRvIII in human cancers. A detailed discussion of the formation of EGFRvIII and its structure at the protein level are likewise included along with a discussion of its more functional roles. The design and use (preclinical and clinical) of small molecule inhibitors, antibodies, and antisense oligonucleotides against wild-type EGFR are considered in detail as these strategies can be directly adapted to target EGFRvIII. Finally, the status of EGFRvIII targeted therapy is reviewed.
引用
收藏
页码:745 / 760
页数:16
相关论文
共 107 条
[1]   Disulfide bond structure of human epidermal growth factor receptor [J].
Abe, Y ;
Odaka, M ;
Inagaki, F ;
Lax, I ;
Schlessinger, J ;
Kohda, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) :11150-11157
[2]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[3]  
ALBANELL J, 2000, P NCI EORTC ACCR S, V6, P383
[4]   Constitutive activation of c-Jun N-terminal kinase by a mutant epidermal growth factor receptor [J].
Antonyak, MA ;
Moscatello, DK ;
Wong, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :2817-2822
[5]  
Archer GE, 1999, CLIN CANCER RES, V5, P2646
[6]   A genetically modified allogeneic cellular vaccine generates MHC class I-restricted cytotoxic responses against tumor-associated antigens and protects against CNS tumors in vivo [J].
Ashley, DM ;
Sampson, JH ;
Archer, GE ;
Batra, SK ;
Bigner, DD ;
Hale, LP .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 78 (1-2) :34-46
[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]  
BASELGA J, 2000, SIGNAL, V1, P12
[9]  
BASELGA J, 2000, AACR NCI EORTC, P29
[10]  
BATRA SK, 1995, CELL GROWTH DIFFER, V6, P251