Hyperinsulinaemia in cancer

被引:136
作者
Gallagher, Emily J. [1 ,2 ]
LeRoith, Derek [1 ,2 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Med, Div Endocrinol Diabet & Bone Dis, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Tisch Canc Inst Mt Sinai, New York, NY 10029 USA
关键词
INSULIN-RECEPTOR EXPRESSION; GLUCOSE COTRANSPORTER 2; MAMMARY-TUMOR GROWTH; DIET-INDUCED OBESITY; BODY-MASS INDEX; BREAST-CANCER; CELL-PROLIFERATION; C-PEPTIDE; PANCREATIC-CANCER; MOUSE MODEL;
D O I
10.1038/s41568-020-0295-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Elevated circulating insulin levels are frequently observed in the setting of obesity and early type 2 diabetes, as a result of insensitivity of metabolic tissues to the effects of insulin. Higher levels of circulating insulin have been associated with increased cancer risk and progression in epidemiology studies. Elevated circulating insulin is believed to be a major factor linking obesity, diabetes and cancer. With the development of targeted cancer therapies, insulin signalling has emerged as a mechanism of therapeutic resistance. Although metabolic tissues become insensitive to insulin in the setting of obesity, a number of mechanisms allow cancer cells to maintain their ability to respond to insulin. Significant progress has been made in the past decade in understanding the insulin receptor and its signalling pathways in cancer, and a number of lessons have been learnt from therapeutic failures. These discoveries have led to numerous clinical trials that have aimed to reduce the levels of circulating insulin and to abrogate insulin signalling in cancer cells. With the rising prevalence of obesity and diabetes worldwide, and the realization that hyperinsulinaemia may contribute to therapeutic failures, it is essential to understand how insulin and insulin receptor signalling promote cancer progression. This Review discusses the current understanding of how insulin and insulin receptor signalling contribute to cancer growth, in the context of the rising prevalence of obesity and diabetes worldwide and the realization that hyperinsulinaemia may contribute to therapeutic failures.
引用
收藏
页码:629 / 644
页数:16
相关论文
共 195 条
[1]   Role of Sodium-Glucose Cotransporter 2 (SGLT 2) Inhibitors in the Treatment of Type 2 Diabetes [J].
Abdul-Ghani, Muhammad A. ;
Norton, Luke ;
DeFronzo, Ralph A. .
ENDOCRINE REVIEWS, 2011, 32 (04) :515-531
[2]  
Agency E. M, 2018, ASS REP STEGL, V2020
[3]   Pancreatic β Cell Regeneration as a Possible Therapy for Diabetes [J].
Aguayo-Mazzucato, Cristina ;
Bonner-Weir, Susan .
CELL METABOLISM, 2018, 27 (01) :57-67
[4]   Expression of IGF/insulin receptor in prostate cancer tissue and progression to lethal disease [J].
Ahearn, Thomas U. ;
Peisch, Sam ;
Pettersson, Andreas ;
Ebot, Ericka M. ;
Zhou, Cindy Ke ;
Graff, Rebecca E. ;
Sinnott, Jennifer A. ;
Fazli, Ladan ;
Judson, Gregory L. ;
Bismar, Tarek A. ;
Rider, Jennifer R. ;
Gerke, Travis ;
Chan, June M. ;
Fiorentino, Michelangelo ;
Flavin, Richard ;
Sesso, Howard D. ;
Finn, Stephen ;
Giovannucci, Edward L. ;
Gleave, Martin ;
Loda, Massimo ;
Li, Zhe ;
Pollak, Michael ;
Mucci, Lorelei A. .
CARCINOGENESIS, 2018, 39 (12) :1431-1437
[5]   HMGA1 protein is a positive regulator of the insulin-like growth factor-I receptor gene [J].
Aiello, Aurora ;
Pandini, Giuseppe ;
Sarfstein, Rive ;
Werner, Haim ;
Manfioletti, Guidalberto ;
Vigneri, Riccardo ;
Belfiore, Antonino .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (10) :1919-1926
[6]   Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity [J].
Alberti, K. G. M. M. ;
Eckel, Robert H. ;
Grundy, Scott M. ;
Zimmet, Paul Z. ;
Cleeman, James I. ;
Donato, Karen A. ;
Fruchart, Jean-Charles ;
James, W. Philip T. ;
Loria, Catherine M. ;
Smith, Sidney C., Jr. .
CIRCULATION, 2009, 120 (16) :1640-1645
[7]   Nuclear IGF1R Interacts with Regulatory Regions of Chromatin to Promote RNA Polymerase II Recruitment and Gene Expression Associated with Advanced Tumor Stage [J].
Aleksic, Tamara ;
Gray, Nicki ;
Wu, Xiaoning ;
Rieunier, Guillaume ;
Osher, Eliot ;
Mills, Jack ;
Verrill, Clare ;
Bryant, Richard J. ;
Han, Cheng ;
Hutchinson, Kathryn ;
Lambert, Adam G. ;
Kumar, Rajeev ;
Hamdy, Freddie C. ;
Weyer-Czernilofsky, Ulrike ;
Sanderson, Michael P. ;
Bogenrieder, Thomas ;
Taylor, Stephen ;
Macaulay, Valentine M. .
CANCER RESEARCH, 2018, 78 (13) :3497-3509
[8]   IGF-1R associates with adverse outcomes after radical radiotherapy for prostate cancer [J].
Aleksic, Tamara ;
Verrill, Clare ;
Bryant, Richard J. ;
Han, Cheng ;
Worrall, Andrew Ross ;
Brureau, Laurent ;
Larre, Stephane ;
Higgins, Geoff S. ;
Fazal, Fahad ;
Sabbagh, Ahmad ;
Haider, Syed ;
Buffa, Francesca M. ;
Cole, David ;
Macaulay, Valentine M. .
BRITISH JOURNAL OF CANCER, 2017, 117 (11) :1600-1606
[9]   The Insulin Receptor Translocates to the Nucleus to Regulate Cell Proliferation in Liver [J].
Amaya, Maria J. ;
Oliveira, Andre G. ;
Guimaraes, Erika S. ;
Casteluber, Marisa C. F. ;
Carvalho, Sandhra M. ;
Andrade, Lidia M. ;
Pinto, Mauro C. X. ;
Mennone, Albert ;
Oliveira, Cleida A. ;
Resende, Rodrigo R. ;
Menezes, Gustavo B. ;
Nathanson, Michael H. ;
Fatima Leite, M. .
HEPATOLOGY, 2014, 59 (01) :274-283
[10]   Diabetes, Pancreatogenic Diabetes, and Pancreatic Cancer [J].
Andersen, Dana K. ;
Korc, Murray ;
Petersen, Gloria M. ;
Eibl, Guido ;
Li, Donghui ;
Rickels, Michael R. ;
Chari, Suresh T. ;
Abbruzzese, James L. .
DIABETES, 2017, 66 (05) :1103-1110