Effects of mutations in Wnt/β-catenin, hedgehog, Notch and PI3K pathways on GSK-3 activity-Diverse effects on cell growth, metabolism and cancer

被引:128
作者
McCubrey, James A. [1 ]
Rakus, Dariusz [2 ]
Gizak, Agnieszka [2 ]
Steelman, Linda S. [1 ]
Abrams, Steve L. [1 ]
Lertpiriyapong, Kvin [3 ]
Fitzgerald, Timothy L. [4 ]
Yang, Li V. [5 ]
Montalto, Giuseppe [6 ,7 ]
Cervello, Melchiorre [7 ]
Libra, Massimo [8 ]
Nicoletti, Ferdinando [8 ]
Scalisi, Aurora [9 ]
Torino, Francesco [10 ]
Fenga, Concettina [11 ]
Neri, Luca M. [12 ]
Marmiroli, Sandra [13 ]
Cocco, Lucio [14 ]
Martelli, Alberto M. [14 ]
机构
[1] East Carolina Univ, Brody Sch Med, Dept Microbiol & Immunol, Greenville, NC 27858 USA
[2] Univ Wroclaw, Inst Expt Biol, Dept Anim Mol Physiol, Wroclaw, Poland
[3] East Carolina Univ, Brody Sch Med, Dept Comparat Med, Greenville, NC 27858 USA
[4] East Carolina Univ, Brody Sch Med, Dept Surg, Greenville, NC 27858 USA
[5] East Carolina Univ, Brody Sch Med, Hematol Oncol Sect, Dept Internal Med, Greenville, NC 27858 USA
[6] Univ Palermo, Biomed Dept Internal Med & Specialties, Palermo, Italy
[7] CNR, Ist Biomed & Immunol Mol Alberto Monroy, Palermo, Italy
[8] Univ Catania, Dept Biomed Sci, Catania, Italy
[9] ASP Catania, Unit Oncol Dis, I-95100 Catania, Italy
[10] Univ Roma Tor Vergata, Dept Syst Med, Chair Med Oncol, Rome, Italy
[11] Univ Messina, Policlin G Martino, Occupat Med Sect, Dept Biomed Odontoiatrt Morphol & Funct Images, I-98125 Messina, Italy
[12] Univ Ferrara, Dept Morphol Surg & Expt Med, Ferrara, Italy
[13] Univ Modena & Reggio Emilia, Dept Surg Med Dent & Morphol, Modena, Italy
[14] Univ Bologna, Dipartimento Sci Biomed & Neuromotorie, Bologna, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2016年 / 1863卷 / 12期
关键词
GSK-3; Wnt/beta-catenin; PI3K; Akt; mTOR; Hedgehog; Notch; Targeted therapy; Therapy resistance; GLYCOGEN-SYNTHASE KINASE-3; NF-KAPPA-B; WNT SIGNALING PATHWAY; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA CELLS; LUNG ADENOCARCINOMA CELLS; MESSENGER-RNA EXPRESSION; HEREDITARY BREAST-CANCER; EMBRYONIC STEM-CELLS; PANCREATIC-CANCER;
D O I
10.1016/j.bbamcr.2016.09.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycogen synthase kinase-3 (GSK-3) is a serine/threonine kinase that participates in an array of critical cellular processes. GSK-3 was first characterized as an enzyme that phosphorylated and inactivated glycogen synthase. However, subsequent studies have revealed that this moon-lighting protein is involved in numerous signaling pathways that regulate not only metabolism but also have roles in: apoptosis, cell cycle progression, cell renewal, differentiation, embiyogenesis, migration, regulation of gene transcription, stem cell biology and survival. In this review, we will discuss the roles that GSK-3 plays in various diseases as well as how this pivotal kinase interacts with multiple signaling pathways such as: PI3K/PTEN/Akt/mTOR, Ras/Raf/MEK/ERK, Wnt/beta-catenin, hedgehog, Notch and TP53. Mutations that occur in these and other pathways can alter the effects that natural GSK-3 activity has on regulating these signaling circuits that can lead to cancer as well as other diseases. The novel roles that microRNAs play in regulation of the effects of GSK-3 will also be evaluated. Targeting GSK-3 and these other pathways may improve therapy and overcome therapeutic resistance. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:2942 / 2976
页数:35
相关论文
共 497 条
[81]   6-Bromoindirubin-3′oxime (BIO) decreases proliferation and migration of canine melanoma cell lines [J].
Chon, Esther ;
Flanagan, Brandi ;
Rodrigues, Lucas Campos de Sa ;
Piskun, Caroline ;
Stein, Timothy J. .
VETERINARY JOURNAL, 2015, 205 (02) :305-312
[82]   Clinical and molecular characterization of HER2 amplified-pancreatic cancer [J].
Chou, Angela ;
Waddell, Nicola ;
Cowley, Mark J. ;
Gill, Anthony J. ;
Chang, David K. ;
Patch, Ann-Marie ;
Nones, Katia ;
Wu, Jianmin ;
Pinese, Mark ;
Johns, Amber L. ;
Miller, David K. ;
Kassahn, Karin S. ;
Nagrial, Adnan M. ;
Wasan, Harpreet ;
Goldstein, David ;
Toon, Christopher W. ;
Chin, Venessa ;
Chantrill, Lorraine ;
Humphris, Jeremy ;
Mead, R. Scott ;
Rooman, Ilse ;
Samra, Jaswinder S. ;
Pajic, Marina ;
Musgrove, Elizabeth A. ;
Pearson, John V. ;
Morey, Adrienne L. ;
Grimmond, Sean M. ;
Biankin, Andrew V. .
GENOME MEDICINE, 2013, 5
[83]   GSK3β regulates BCL2L12 and BCL2L12A anti-apoptosis signaling in glioblastoma and is inhibited by LiCl [J].
Chou, Chia-Hua ;
Chou, An-Kuo ;
Lin, Ching-Chih ;
Chen, Wei-Jay ;
Wei, Chih-Chang ;
Yang, Ming-Chang ;
Hsu, Ching-Mei ;
Lung, For-Wey ;
Loh, Joon-Khim ;
Howng, Shen-Long ;
Hong, Yi-Ren .
CELL CYCLE, 2012, 11 (03) :532-542
[84]   Activation of signal transduction pathways during hepatic oncogenesis [J].
Chung, Waihong ;
Kim, Miran ;
de la Monte, Suzanne ;
Longato, Lisa ;
Carlson, Rolf ;
Slagle, Betty L. ;
Dong, Xiaoqun ;
Wands, Jack R. .
CANCER LETTERS, 2016, 370 (01) :1-9
[85]  
Ciuffreda Ludovica, 2014, Advances in Biological Regulation, V56, P66, DOI 10.1016/j.jbior.2014.07.002
[86]   Wnt/β-Catenin Signaling and Disease [J].
Clevers, Hans ;
Nusse, Roel .
CELL, 2012, 149 (06) :1192-1205
[87]   Azacitidine-resistant SKM1 myeloid cells are defective for AZA-induced mitochondrial apoptosis and autophagy [J].
Cluzeau, Thomas ;
Robert, Guillaume ;
Puissant, Alexandre ;
Jean-Michel, Karsenti ;
Cassuto, Jill-Patrice ;
Raynaud, Sophie ;
Auberger, Patrick .
CELL CYCLE, 2011, 10 (14) :2339-2343
[88]   Loss of miR-200c: A Marker of Aggressiveness and Chemoresistance in Female Reproductive Cancers [J].
Cochrane, Dawn R. ;
Howe, Erin N. ;
Spoelstra, Nicole S. ;
Richer, Jennifer K. .
JOURNAL OF ONCOLOGY, 2010, 2010
[89]   MicroRNA-200c mitigates invasiveness and restores sensitivity to microtubule-targeting chemotherapeutic agents [J].
Cochrane, Dawn R. ;
Spoelstra, Nicole S. ;
Howe, Erin N. ;
Nordeen, Steven K. ;
Richer, Jennifer K. .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (05) :1055-1066
[90]   Further evidence that the tyrosine phosphorylation of glycogen synthase kinase-3 (GSK3) in mammalian cells is an autophosphorylation event [J].
Cole, A ;
Frame, S ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2004, 377 :249-255