Anti-insulin-like growth factor strategies in breast cancer

被引:16
|
作者
Jerome, L
Shiry, L
Leyland-Jones, B
机构
[1] McGill Univ, Dept Oncol, Montreal, PQ H2W 1S6, Canada
[2] Insmed Inc, Richmond, VA USA
关键词
D O I
10.1053/j.seminoncol.2004.01.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The insulin-like growth factors (IGF-I and -II) are potent mitogens and survival factors for both normal and malignant breast cells. These effects are mediated primarily through the IGF-I receptor (IGF-IR), which is significantly overexpressed and highly activated in breast tumors. The IGF-binding proteins are competitive inhibitors of IGF/IGF-IR interaction, limiting cellular proliferation and survival. Higher serum IGF-I levels or an increased ratio of IGF-I to IGF binding protein-3 is associated with an increased risk of developing breast cancer. Hence, interest in the IGF system as a potential target for the development of novel antineoplastic therapies has ensued. Several strategies to interrupt IGF-IR signaling are currently being evaluated for the treatment of breast cancer, including suppression of IGF production, reduction of functional IGF-IR levels, neutralization of IGF action, and inhibition of IGF-IR activation. © 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:54 / 63
页数:10
相关论文
共 50 条
  • [2] Down-regulation of insulin receptor by antibodies against the type I insulin-like growth factor receptor: Implications for anti-insulin-like growth factor therapy in breast cancer
    Sachdev, D
    Singh, R
    Fujita-Yamaguchi, Y
    Yee, D
    CANCER RESEARCH, 2006, 66 (04) : 2391 - 2402
  • [3] An anti-insulin-like growth factor I receptor antibody that is a potent inhibitor of cancer cell proliferation
    Maloney, EK
    McLaughlin, JL
    Dagdigian, NE
    Garrett, LM
    Connors, KM
    Zhou, XM
    Blättler, WA
    Chittenden, T
    Singh, R
    CANCER RESEARCH, 2003, 63 (16) : 5073 - 5083
  • [4] Antiproliferative and apoptotic effects of a specific anti-insulin-like growth factor I receptor single chain antibody on breast cancer cells
    Motallebnezhad, Morteza
    Younesi, Vahid
    Aghebati-Maleki, Leili
    Nickho, Hamid
    Safarzadeh, Elham
    Ahmadi, Majid
    Movassaghpour, Ali Akbar
    Hosseini, Ahmad
    Yousefi, Mehdi
    TUMOR BIOLOGY, 2016, 37 (11) : 14841 - 14850
  • [5] Molecular predictors of response to a humanized anti-insulin-like growth factor-I receptor monoclonal antibody in breast and colorectal cancer
    Zha, Jiping
    O'Brien, Carol
    Savage, Heidi
    Huw, Ling-Yuh
    Zhong, Fiona
    Berry, Leanne
    Phillips, Gail D. Lewis
    Luis, Elizabeth
    Cavet, Guy
    Hu, Xiaolan
    Amler, Lukas C.
    Lackner, Mark R.
    MOLECULAR CANCER THERAPEUTICS, 2009, 8 (08) : 2110 - 2121
  • [6] Anti-insulin-like growth factor-1 autoantibodies in type 1 diabetes
    Maruyama, T
    Murayama, H
    Nagata, A
    Shimada, A
    Kasuga, A
    Saruta, T
    IMMUNOLOGY OF DIABETES: AUTOIMMUNE MECHANISMS AND THE PREVENTION AND CURE OF TYPE 1 DIABETES, 2002, 958 : 267 - 270
  • [7] An overview of currently available anti-insulin-like growth factor I receptor antibodies
    Kusada, Yu
    Fujita-Yamaguchi, Yoko
    BIOSCIENCE TRENDS, 2007, 1 (03) : 128 - 133
  • [8] Bevacizumab reduces tumor targeting of antiepidermal growth factor and anti-insulin-like growth factor 1 receptor antibodies
    Heskamp, Sandra
    Boerman, Otto C.
    Molkenboer-Kuenen, Janneke D. M.
    Oyen, Wim J. G.
    van der Graaf, Winette T. A.
    van Laarhoven, Hanneke W. M.
    INTERNATIONAL JOURNAL OF CANCER, 2013, 133 (02) : 307 - 314
  • [9] Bevacizumab prevents effective targeting of anti-epidermal growth factor and anti-insulin-like growth factor 1 receptor antibodies
    Heskamp, S.
    van Laarhoven, H. W. M.
    Molkenboer-Kuenen, J. D. M.
    van der Graaf, W. T. A.
    Oyen, W. J. G.
    Boerman, O. C.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2012, 39 : S160 - S160
  • [10] Bevacizumab treatment reduces targeting of anti-epidermal growth factor receptor and anti-insulin-like growth factor 1 receptor antibodies
    Heskamp, Sandra
    van Laarhoven, Hanneke
    Molkenboer-Kuenen, Janneke
    Oyen, Wim
    van der Graaf, Winette
    Boerman, Otto
    JOURNAL OF NUCLEAR MEDICINE, 2012, 53