IGF system in cancer: from bench to clinic

被引:48
作者
Chaves, Jorge [2 ]
Saif, Muhammad Wasif [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[2] Yale Univ, Sch Med, New York, NY USA
关键词
cancer; insulin-like growth factors; insulin-like growth factors binding proteins; GROWTH-FACTOR-I; INSULIN-RECEPTOR ISOFORM; MULTIPLE SIGNALING PATHWAYS; TUMOR-GROWTH; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; HYBRID RECEPTORS; BINDING-PROTEIN; LIGAND-BINDING; CELL-GROWTH;
D O I
10.1097/CAD.0b013e32834258a1
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Insulin-like growth factors (IGFs) are important mediators of growth, development, and survival, and have been implicated in the pathogenesis of malignancies. The IGF system is a complex system comprising two growth factors (IGF-I and IGF-II), cell surface receptors (IGF-IR and IGF-IIR), six specific high-affinity binding proteins (IGFBP-1 to IGFBP-6), IGFBP proteases, and several other IGFBP-interacting molecules that regulate and propagate IGF actions in several tissues. IGFs are produced by almost any cell in the body; circulate in more than 1000-fold higher concentrations than most other peptide hormones, such as insulin, and their action is modulated by several binding proteins. Studies have revealed that IGFs may promote cell cycle progression and inhibition of apoptosis either by directly associating with other growth factors or indirectly by interacting with other molecular systems that have an established role in carcinogenesis and cancer promotion, such as steroid hormones and integrins. In addition, studies also suggest that increased serum levels of IGFs and/or altered levels of their binding proteins are associated with increased risk of developing cancers. These data underline the significance of IGFs system in the development of cancer risk, and a potential target for novel anticancer treatments and/or preventative strategies in high-risk groups. The researchers review the IGFs pathway and its implications in cancer development and treatment. Anti-Cancer Drugs 22: 206-212 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:206 / 212
页数:7
相关论文
共 80 条
[1]
Simultaneous inhibition of IGF1R and Src family kinases causes tumor growth inhibition and tumor regression in xenograft models [J].
Aftab, D. T. .
EJC SUPPLEMENTS, 2006, 4 (12) :178-178
[2]
CLONING AND CHARACTERIZATION OF THE PROMOTER FOR THE RAT INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-3 GENE [J].
ALBISTON, AL ;
SAFFERY, R ;
HERINGTON, AC .
ENDOCRINOLOGY, 1995, 136 (02) :696-704
[3]
Results of a pilot study involving the use of an antisense oligodeoxynucleotide directed against the insulin-like growth factor type I receptor in malignant astrocytomas [J].
Andrews, DW ;
Resnicoff, M ;
Flanders, AE ;
Kenyon, L ;
Curtis, M ;
Merli, G ;
Baserga, R ;
Iliakis, G ;
Aiken, RD .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (08) :2189-2200
[4]
INTERFERENCE OF THE IGF SYSTEM AS A STRATEGY TO INHIBIT BREAST-CANCER GROWTH [J].
ARTEAGA, CL .
BREAST CANCER RESEARCH AND TREATMENT, 1992, 22 (01) :101-106
[5]
BAKER J, 1993, CELL, V75, P73, DOI 10.1016/0092-8674(93)90680-O
[6]
Baserga R, 1997, VITAM HORM, V53, P65, DOI 10.1016/S0083-6729(08)60704-9
[7]
Insulin Receptor Isoforms and Insulin Receptor/Insulin-Like Growth Factor Receptor Hybrids in Physiology and Disease [J].
Belfiore, Antonino ;
Frasca, Francesco ;
Pandini, Giusepe ;
Sciacca, Laura ;
Vigneri, Riccardo .
ENDOCRINE REVIEWS, 2009, 30 (06) :586-623
[8]
BLAT C, 1989, J BIOL CHEM, V264, P12449
[9]
Substrate competitive inhibitors of IGF-1 receptor kinase [J].
Blum, G ;
Gazit, A ;
Levitzki, A .
BIOCHEMISTRY, 2000, 39 (51) :15705-15712
[10]
Burtrum D, 2003, CANCER RES, V63, P8912