Targeting the Insulin Growth Factor Receptor 1

被引:69
作者
Arnaldez, Fernanda I. [1 ]
Heiman, Lee J. [1 ]
机构
[1] NCI, NIH, Mol Oncol Sect, Pediat Oncol Branch,Ctr Canc Res, Bethesda, MD 20892 USA
关键词
IGF1R; IGF1; IGF2; Insulin; Kinase; Cancer; FACTOR-I RECEPTOR; HUMAN-BREAST-CANCER; GASTROINTESTINAL-STROMAL-TUMORS; SMALL-MOLECULE INHIBITORS; IGF-BINDING PROTEIN-3; MONOCLONAL-ANTIBODY; ACQUIRED-RESISTANCE; HYBRID RECEPTORS; PROSTATE-CANCER; GENE-EXPRESSION;
D O I
10.1016/j.hoc.2012.01.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The IGF axis is a tightly controlled endocrine system that regulates cell growth and development, known to have an important function in cancer biology. IGF1 and IGF2 can promote cancer growth in a GH-independent manner both through paracrine and autocrine secretion and can also confer resistance to chemotherapy and radiation. Many alterations of this system have been found in neoplasias, including increased expression of ligands and receptors, loss of heterozygosity of the IGF2 locus and increased IGF1R gene copy number. The IGF1 network is an attractive candidate for targeted therapy, including receptor blockade with monoclonal antibodies and small molecule inhibitors of receptor downstream signaling. This article reviews the role of the IGF axis in the initiation and progression of cancer, and describes the recent advances in IGF inhibition as a therapeutic tool.
引用
收藏
页码:527 / +
页数:18
相关论文
共 127 条
[1]   Growth patterns and the risk of breast cancer in women [J].
Ahlgren, M ;
Melbye, M ;
Wohlfahrt, J ;
Sorensen, TIA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (16) :1619-1626
[2]   Recombinant human insulin-like growth factor-binding protein 3 inhibits tumor growth and targets the Akt pathway in lung and colon cancer models [J].
Alami, Nezha ;
Page, Viviane ;
Yu, Qingnan ;
Jerome, Lori ;
Paterson, Jesse ;
Shiry, Laura ;
Leyland-Jones, Brian .
GROWTH HORMONE & IGF RESEARCH, 2008, 18 (06) :487-496
[3]  
All-Ericsson C, 2002, INVEST OPHTH VIS SCI, V43, P1
[4]   EFFECT OF DIABETES AND ITS CONTROL ON INSULIN-LIKE GROWTH-FACTORS IN THE YOUNG SUBJECT WITH TYPE-I DIABETES [J].
AMIEL, SA ;
SHERWIN, RS ;
HINTZ, RL ;
GERTNER, JM ;
PRESS, CM ;
TAMBORLANE, WV .
DIABETES, 1984, 33 (12) :1175-1179
[5]  
[Anonymous], NOVARTIS FDN S
[6]  
[Anonymous], J CLIN ONCOL S
[7]   Increased Insulin-Like Growth Factor 1 Receptor Protein Expression and Gene Copy Number in Small Cell Lung Cancer [J].
Badzio, Andrzej ;
Wynes, Murry W. ;
Dziadziuszko, Rafal ;
Merrick, Daniel T. ;
Pardo, Marta ;
Rzyman, Witold ;
Kowalczyk, Anna ;
Singh, Shalini ;
Ranger-Moore, James ;
Manriquez, Guadalupe ;
Gaire, Fabien ;
Jassem, Jacek ;
Hirsch, Fred R. .
JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (12) :1905-1911
[8]   Activation of ErbB-2 via a hierarchical interaction between ErbB-2 and type I insulin-like growth factor receptor in mammary tumor cells [J].
Balañá, ME ;
Labriola, L ;
Salatino, M ;
Movsichoff, F ;
Peters, G ;
Charreau, EH ;
Elizalde, PV .
ONCOGENE, 2001, 20 (01) :34-47
[9]   A Distinct Spectrum of Copy Number Aberrations in Pediatric High-Grade Gliomas [J].
Bax, Dorine A. ;
Mackay, Alan ;
Little, Suzanne E. ;
Carvalho, Diana ;
Viana-Pereira, Marta ;
Tamber, Narinder ;
Grigoriadis, Anita E. ;
Ashworth, Alan ;
Reis, Rui M. ;
Ellison, David W. ;
Al-Sarraj, Safa ;
Hargrave, Darren ;
Jones, Chris .
CLINICAL CANCER RESEARCH, 2010, 16 (13) :3368-3377
[10]  
Beech DJ, 2001, ONCOL REP, V8, P325