The type I insulin-like growth factor receptor pathway: a key player in cancer therapeutic resistance

被引:105
作者
Casa, Angelo J. [2 ,3 ]
Dearth, Robert K. [2 ,3 ]
Litzenburger, Beate C. [2 ,3 ]
Lee, Adrian V. [2 ,3 ]
Cui, Xiaojiang [1 ]
机构
[1] St Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
[2] Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
breast cancer; chemotherapy; EGFR; endocrine therapy; estrogen receptor; HER2; IGF; IGF-IR; radiation; targeted therapy; therapeutic resistance;
D O I
10.2741/2925
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The insulin-like growth factor (IGF) ligands stimulate cellular proliferation and survival by activating the type I insulin-like growth factor receptor (IGF-IR). As a result, the IGF signaling system is implicated in a number of cancers, including those of the breast, prostate, and lung. In addition to mitogenic and anti-apoptotic roles that may directly influence tumor development, IGF-IR also appears to be a critical determinant of response to numerous cancer therapies. This review describes the role of the IGF-IR pathway in mediating resistance to both general cytotoxic therapies, such as radiation and chemotherapy, and targeted therapies, such as tamoxifen and trastuzumab. It concludes with a description of approaches to target IGF-IR and argues that inhibition of IGF signaling, in conjunction with standard therapies, may enhance the response of cancer cells to multiple modalities.
引用
收藏
页码:3273 / 3287
页数:15
相关论文
共 131 条
[1]   A phase I trial to assess the pharmacology of the new oestrogen receptor antagonist fulvestrant on the endometrium in healthy postmenopausal volunteers [J].
Addo, S ;
Yates, RA ;
Laight, A .
BRITISH JOURNAL OF CANCER, 2002, 87 (12) :1354-1359
[2]   Insulin-like growth factor-I receptor signaling blockade combined with radiation [J].
Allen, Gregory W. ;
Saba, Corey ;
Armstrong, Eric A. ;
Huang, Shyh-Min ;
Benavente, Sergio ;
Ludwig, Dale L. ;
Hicklin, Daniel J. ;
Harari, Paul M. .
CANCER RESEARCH, 2007, 67 (03) :1155-1162
[3]   BLOCKADE OF THE TYPE-I SOMATOMEDIN RECEPTOR INHIBITS GROWTH OF HUMAN-BREAST CANCER-CELLS IN ATHYMIC MICE [J].
ARTEAGA, CL ;
KITTEN, LJ ;
CORONADO, EB ;
JACOBS, S ;
KULL, FC ;
ALLRED, DC ;
OSBORNE, CK .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) :1418-1423
[4]   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
[5]  
Beech DJ, 2001, ONCOL REP, V8, P325
[6]   Tumour necrosis factor and PI3-kinase control oestrogen receptor alpha protein level and its transrepression function [J].
Bhat-Nakshatri, P ;
Campbell, RA ;
Patel, NM ;
Newton, TR ;
King, AJ ;
Marshall, MS ;
Ali, S ;
Nakshatri, H .
BRITISH JOURNAL OF CANCER, 2004, 90 (04) :853-859
[7]   Variable apoptotic response of NSCLC cells to inhibition of the MEK/ERK pathway by small molecules or dominant negative mutants [J].
Brognard, J ;
Dennis, PA .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (09) :893-904
[8]  
Brognard J, 2001, CANCER RES, V61, P3986
[9]   Inhibition of insulin-like growth factor-1 receptor signaling enhances growth-inhibitory and proapoptotic effects of gefitinib (Iressa) in human breast cancer cells [J].
Camirand, A ;
Zakikhani, M ;
Young, F ;
Pollak, M .
BREAST CANCER RESEARCH, 2005, 7 (04) :R570-R579
[10]   Phosphatidylinositol 3-kinase/AKT-mediated activation of estrogen receptor α -: A new model for anti-estrogen resistance [J].
Campbell, RA ;
Bhat-Nakshatri, P ;
Patel, NM ;
Constantinidou, D ;
Ali, S ;
Nakshatri, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9817-9824