Role of the insulin-like growth factor family in cancer development and progression

被引:1146
作者
Yu, H
Rohan, T
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Feist Weiller Canc Ctr, Shreveport, LA 71130 USA
[2] Albert Einstein Coll Med, Dept Epidemiol & Social Med, Bronx, NY 10467 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2000年 / 92卷 / 18期
关键词
D O I
10.1093/jnci/92.18.1472
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The insulin-like growth factors (IGFs) are mitogens that play a pivotal role in regulating cell proliferation, differentiation, and apoptosis. The effects of IGFs are mediated through the ICF-I receptor, which is also involved in cell transformation induced by tumor virus proteins and oncogene products. Six IGF-binding proteins (IGFBPs) can inhibit or enhance the actions of IGFs. These opposing effects are determined by the structures of the binding proteins. The effects of IGFBPs on IGFs are regulated in part by IGFBP proteases. Laboratory studies have shown that IGFs exert strong mitogenic and antiapoptotic actions on various cancer cells. IGFs also act synergistically with other mitogenic growth factors and steroids and antagonize the effect of antiproliferative molecules on cancer growth. The role of IGFs in cancer is supported by epidemiologic studies, which have found that high levels of circulating IGF-I and low levels of IGFBP-3 are associated with increased risk of several common cancers, including those of the prostate, breast, colorectum, and lung. Evidence further suggests that certain lifestyles, such as one involving a high-energy diet, may increase IGF-I levels, a finding that is supported by animal experiments indicating that IGFs may abolish the inhibitory effect of energy restriction on cancer growth. Further investigation of the role of IGFs in linking high energy intake, increased cell proliferation, suppression of apoptosis, and increased cancer risk may provide new insights into the etiology of cancer and lead to new strategies for cancer prevention.
引用
收藏
页码:1472 / 1489
页数:18
相关论文
共 324 条
[1]  
Agurs-Collins T., 1999, Proceedings of the American Association for Cancer Research Annual Meeting, V40, P152
[2]  
ALLANDER SV, 1994, J BIOL CHEM, V269, P10891
[3]   AUTOCRINE REGULATION OF CELL-PROLIFERATION BY THE INSULIN-LIKE GROWTH-FACTOR (IGF) AND IGF BINDING PROTEIN-3 PROTEASE SYSTEM IN A HUMAN PROSTATE CARCINOMA CELL-LINE (PC-3) [J].
ANGELLOZNICOUD, P ;
BINOUX, M .
ENDOCRINOLOGY, 1995, 136 (12) :5485-5492
[4]   Increased circulating levels of insulin-like growth factor-I and decreased circulating levels of insulin-like growth factor binding protein-1 in postmenopausal women with endometrial cancer [J].
Ayabe, T ;
Tsutsumi, O ;
Sakai, H ;
Yoshikawa, H ;
Yano, T ;
Kurimoto, F ;
Taketani, Y .
ENDOCRINE JOURNAL, 1997, 44 (03) :419-424
[5]  
BACHRACH LK, 1995, GROWTH REGULAT, V5, P109
[6]   Postoperative induction of insulin-like growth factor binding protein-3 proteolytic activity: Relation to insulin and insulin sensitivity [J].
Bang, P ;
Nygren, J ;
Carlsson-Skwirut, C ;
Thorell, A ;
Ljungqvist, O .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (07) :2509-2515
[7]   Human pregnancy serum contains at least two distinct proteolytic activities with the ability to degrade insulin-like growth factor finding protein-3 [J].
Bang, P ;
Fielder, PJ .
ENDOCRINOLOGY, 1997, 138 (09) :3912-3917
[8]   SERUM LEVELS OF INSULIN-LIKE GROWTH-FACTOR-I IN OPERABLE BREAST-CANCER IN RELATION TO THE MAIN PROGNOSTIC VARIABLES AND THEIR PERIOPERATIVE CHANGES IN RELATION TO THOSE OF PROLACTIN [J].
BARNI, S ;
LISSONI, P ;
BRIVIO, F ;
FUMAGALLI, L ;
MERLINI, D ;
CATALDO, M ;
ROVELLI, F ;
TANCINI, G .
TUMORI, 1994, 80 (03) :212-215
[9]  
BASERGA R, 1995, CANCER RES, V55, P249
[10]   MAMMARY-CANCER IN TRANSGENIC MICE EXPRESSING INSULIN-LIKE GROWTH-FACTOR-II (IGF-II) [J].
BATES, P ;
FISHER, R ;
WARD, A ;
RICHARDSON, L ;
HILL, DJ ;
GRAHAM, CF .
BRITISH JOURNAL OF CANCER, 1995, 72 (05) :1189-1193