New advances on the functional cross-talk between insulin-like growth factor-I and estrogen signaling in cancer

被引:71
作者
Bartella, Viviana [1 ]
De Marco, Paola [1 ]
Malaguarnera, Roberta [2 ]
Belfiore, Antonino [2 ]
Maggiolini, Marcello [2 ]
机构
[1] Univ Calabria, Dept Pharmacobiol, I-87030 Arcavacata Di Rende, Italy
[2] Magna Graecia Univ Catanzaro, Endocrinol Dept Hlth, I-88100 Catanzaro, Italy
关键词
Insulin-like growth factor-I; Estrogens; Estrogen receptors; GPER; Cancer; HUMAN BREAST-CANCER; PROTEIN-COUPLED RECEPTOR; STIMULATES C-FOS; IGF-I; BINDING-PROTEINS; EPITHELIAL-CELLS; FACTOR SYSTEM; PROGESTERONE-RECEPTOR; ENDOCRINE RESISTANCE; STEROID-RECEPTORS;
D O I
10.1016/j.cellsig.2012.03.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There is increasing awareness that estrogens may affect cell functions through the integration with a network of signaling pathways. The IGF system is a phylogenetically highly conserved axis that includes the insulin receptor (IR) and the insulin-like growth factor I receptor (IGF-IR) pathways, which are of crucial importance in the regulation of metabolism and cell growth in relationship to nutrient availability. Numerous studies nowadays document that estrogens cooperate with IGF system at multiple levels both in physiology and in disease. Several studies have focused on this bidirectional cross-talk in central nervous system, in mammary gland development and in cancer. Notably, cancer cells show frequent deregulation of the IGF system with overexpression of IR and/or IGF-IR and their ligands as well as frequent upregulation of the classical estrogen receptor (ER)alpha and the novel ER named GPER. Recent studies have, therefore, unraveled further mechanisms of cross-talk involving membrane initiated estrogen actions and the IGF system in cancer, that converge in the stimulation of pro-tumoral effects. These studies offer hope for new strategies aimed at the treatment of estrogen related cancers in order to prevent an estrogen-independent and more aggressive tumor progression. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1515 / 1521
页数:7
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