ERBB receptors and cancer: The complexity of targeted inhibitors

被引:2776
作者
Hynes, NE
Lane, HA
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[2] Novartis Inst Biomed Res, CH-4002 Basel, Switzerland
关键词
D O I
10.1038/nrc1609
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
ERBB receptor tyrosine kinases have important roles in human cancer. In particular, the expression or activation of epidermal growth factor receptor and ERBB2 are altered in many epithelial tumours, and clinical studies indicate that they have important roles in tumour aetiology and progression. Accordingly, these receptors have been intensely studied to understand their importance in cancer biology and as therapeutic targets, and many ERBB inhibitors are now used in the clinic. We will discuss the significance of these receptors as clinical targets, in particular the molecular mechanisms underlying response.
引用
收藏
页码:341 / 354
页数:14
相关论文
共 168 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]
ADNANE J, 1991, ONCOGENE, V6, P659
[3]
Targeting ligand-activated ErbB2 signaling inhibits breast and prostate tumor growth [J].
Agus, DB ;
Akita, RW ;
Fox, WD ;
Lewis, GD ;
Higgins, B ;
Pisacane, PI ;
Lofgren, JA ;
Tindell, C ;
Evans, DP ;
Maiese, K ;
Scher, HI ;
Sliwkowski, MX .
CANCER CELL, 2002, 2 (02) :127-137
[4]
Pharmacodynamic studies of the epidermal growth factor receptor inhibitor ZD1839 in skin from cancer patients: Histopathologic and molecular consequences of receptor inhibition [J].
Albanell, J ;
Rojo, F ;
Averbuch, S ;
Feyereislova, A ;
Mascaro, JM ;
Herbst, R ;
LoRusso, P ;
Rischin, D ;
Sauleda, S ;
Gee, J ;
Nicholson, RI ;
Baselga, J .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) :110-124
[5]
[Anonymous], 1992, Lancet, V339, P1
[6]
[Anonymous], NAT REV CANC
[7]
A role of the kinase mTOR in cellular transformation induced by the oncoproteins P3k and Akt [J].
Aoki, M ;
Blazek, E ;
Vogt, PK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :136-141
[8]
HER-2 amplification, HER-1 expression, and tamoxifen response in estrogen receptor-positive metastatic breast cancer: A southwest oncology group study [J].
Arpino, G ;
Green, SJ ;
Allred, DC ;
Lew, D ;
Martino, S ;
Osborne, CK ;
Elledge, RM .
CLINICAL CANCER RESEARCH, 2004, 10 (17) :5670-5676
[9]
Blockade of epidermal growth factor receptor signaling on tumor cells and tumor-associated endothelial cells for therapy of human carcinomas [J].
Baker, CH ;
Kedar, D ;
McCarty, MF ;
Tsan, R ;
Weber, KL ;
Bucana, CD ;
Fidler, IJ .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (03) :929-938
[10]
Baselga J, 2003, CLIN CANCER RES, V9, P2389