Aiming for the Insulin-like Growth Factor-1 system in breast cancer therapeutics

被引:36
作者
Christopoulos, Panagiotis F. [1 ,2 ,3 ,4 ]
Corthay, Alexandre [2 ,3 ]
Koutsilieris, Michael [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, Dept Expt Physiol, Athens, Greece
[2] Oslo Univ Hosp, Rigshosp, Dept Pathol, Tumor Immunol Lab, POB 4950 Nydalen, N-0424 Oslo, Norway
[3] Univ Oslo, POB 4950 Nydalen, N-0424 Oslo, Norway
[4] UiT Arctic Univ Norway, Fac Hlth Sci, Dept Med Biol, Tromso, Norway
关键词
Insulin-like Growth Factor-1 (IGF-1); Breast cancer; Targeted therapy; Insulin-like Growth Factor-1 Receptor (IGF-1R); Insulin-like Growth Factor Binding Proteins (IGFBPs); Estrogen Receptor (ER); FACTOR-BINDING PROTEIN-4; CARBOXYMETHYL CHITOSAN MICELLES; MAMMARY-GLAND DEVELOPMENT; INHIBITS TUMOR-GROWTH; N-OCTYL-O; IGF-IR; STEM-CELLS; NORDIHYDROGUAIARETIC ACID; MONOCLONAL-ANTIBODY; EPITHELIAL-CELLS;
D O I
10.1016/j.ctrv.2017.11.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the major discoveries occurred in oncology the recent years, breast malignancies remain one of the most common causes of cancer-related deaths for women in developed countries. Development of HER2-targeting drugs has been considered a breakthrough in anti-cancer approaches and alluded to the potential of targeting growth factors in breast cancer (BrCa) therapeutics. More than twenty-five years have passed since the Insulin-like Growth Factor-1 (IGF-1) system was initially recognized as a potential target candidate in BrCa therapy. To date, a growing body of studies have implicated the IGF-1 signaling with the BrCa biology. Despite the promising experimental evidence, the impression from clinical trials is rather disappointing. Several reasons may account for this and the last word regarding the efficacy of this system as a target candidate in BrCa therapeutics is probably not written yet. Herein, we provide the theoretical basis, as well as, a comprehensive overview of the current literature, regarding the different strategies targeting the various components of the IGF-1/IGF-1R axis in several pathophysiological aspects of BrCa, including the tumor micro-environment and cancer sternness. In addition, we review the rationale for targeting the IGF-1 system in the different BrCa molecular subtypes and in treatment resistant breast tumors with a focus on both the molecular mechanisms and on the clinical perspectives of such approaches in specific population subgroups. We also discuss the future challenges, as well as, the development of novel molecules and strategies targeting the system and suggest potential improvements in the field. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 95
页数:17
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