Beyond cell-cell adhesion: Plakoglobin and the regulation of tumorigenesis and metastasis

被引:63
作者
Aktary, Zackie [1 ,2 ]
Alaee, Mahsa [1 ]
Pasdar, Manijeh [1 ]
机构
[1] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
[2] Inst Curie, Orsay, France
关键词
Plakoglobin; gamma-catenin; tumor/metastasis suppressor; p53; gene expression; GAMMA-CATENIN EXPRESSION; ACUTE MYELOID-LEUKEMIA; CADHERIN-MEDIATED ADHESION; SQUAMOUS CARCINOMA-CELLS; CIRCULATING TUMOR-CELLS; WNT SIGNALING PATHWAY; PRION PROTEIN PRPC; BETA-CATENIN; ADHERENS JUNCTIONS; WNT/BETA-CATENIN;
D O I
10.18632/oncotarget.15650
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Plakoglobin (also known as gamma-catenin) is a member of the Armadillo family of proteins and a paralog of beta-catenin. Plakoglobin is a component of both the adherens junctions and desmosomes, and therefore plays a vital role in the regulation of cell-cell adhesion. Similar to beta-catenin, plakoglobin is capable of participating in cell signaling in addition to its role in cell-cell adhesion. In this context, beta-catenin has a well-documented oncogenic potential as a component of the Wnt signaling pathway. In contrast, while some studies have suggested a tumor promoting activity of plakoglobin in a cell/malignancy specific context, it generally acts as a tumor/metastasis suppressor. How plakoglobin acts as a growth/metastasis inhibitory protein has remained, until recently, unclear. Recent evidence suggests that plakoglobin may suppress tumorigenesis and metastasis by multiple mechanisms, including the suppression of oncogenic signaling, interactions with various proteins involved in tumorigenesis and metastasis, and the regulation of the expression of genes involved in these processes. This review is primarily focused on various mechanisms by which plakoglobin may inhibit tumorigenesis and metastasis.
引用
收藏
页码:32270 / 32291
页数:22
相关论文
共 178 条
[1]  
ABERLE H, 1994, J CELL SCI, V107, P3655
[2]   Plakoglobin Is Required for Effective Intermediate Filament Anchorage to Desmosomes [J].
Acehan, Devrim ;
Petzold, Christopher ;
Gumper, Iwona ;
Sabatini, David D. ;
Mueller, Eliane J. ;
Cowin, Pamela ;
Stokes, David L. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2008, 128 (11) :2665-2675
[3]   Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis [J].
Aceto, Nicola ;
Bardia, Aditya ;
Miyamoto, David T. ;
Donaldson, Maria C. ;
Wittner, Ben S. ;
Spencer, Joel A. ;
Yu, Min ;
Pely, Adam ;
Engstrom, Amanda ;
Zhu, Huili ;
Brannigan, Brian W. ;
Kapur, Ravi ;
Stott, Shannon L. ;
Shioda, Toshi ;
Ramaswamy, Sridhar ;
Ting, David T. ;
Lin, Charles P. ;
Toner, Mehmet ;
Haber, Daniel A. ;
Maheswaran, Shyamala .
CELL, 2014, 158 (05) :1110-1122
[4]   Plakoglobin interacts with and increases the protein levels of metastasis suppressor Nm23-H2 and regulates the expression of Nm23-H1 [J].
Aktary, Z. ;
Chapman, K. ;
Lam, L. ;
Lo, A. ;
Ji, C. ;
Graham, K. ;
Cook, L. ;
Li, L. ;
Mackey, J. R. ;
Pasdar, M. .
ONCOGENE, 2010, 29 (14) :2118-2129
[5]   Plakoglobin Represses SATB1 Expression and Decreases In Vitro Proliferation, Migration and Invasion [J].
Aktary, Zackie ;
Pasdar, Manijeh .
PLOS ONE, 2013, 8 (11)
[6]  
Aktary Zackie, 2012, Int J Cell Biol, V2012, P189521, DOI 10.1155/2012/189521
[7]   Plakoglobin interacts with the transcription factor p53 and regulates the expression of 14-3-3σ [J].
Aktary, Zackie ;
Kulak, Stephen ;
Mackey, John ;
Jahroudi, Nadia ;
Pasdar, Manijeh .
JOURNAL OF CELL SCIENCE, 2013, 126 (14) :3031-+
[8]   The three-dimensional molecular structure of the desmosomal plaque [J].
Al-Amoudi, Ashraf ;
Castano-Diez, Daniel ;
Devos, Damien P. ;
Russell, Robert B. ;
Johnson, Graham T. ;
Frangakis, Achilleas S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (16) :6480-6485
[9]   The physical interaction of p53 and plakoglobin is necessary for their synergistic inhibition of migration and invasion [J].
Alaee, Mahsa ;
Padda, Amarjot ;
Mehrabani, Vahedah ;
Churchill, Lucas ;
Pasdar, Manijeh .
ONCOTARGET, 2016, 7 (18) :26898-26915
[10]   Plakoglobin Reduces the in vitro Growth, Migration and Invasion of Ovarian Cancer Cells Expressing N-Cadherin and Mutant p53 [J].
Alaee, Mahsa ;
Danesh, Ghazal ;
Pasdar, Manijeh .
PLOS ONE, 2016, 11 (05)