Causes and consequences of nuclear envelope alterations in tumour progression

被引:78
作者
Bell, Emily S.
Lammerding, Jan
机构
[1] Cornell Univ, Meinig Sch Biomed Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Weill Inst Cell & Mol Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Lamins; Cancer; Signal transduction; Cell migration; Cell mechanics; Gene regulation; A-TYPE LAMINS; EPITHELIAL-MESENCHYMAL TRANSITION; CANCER-CELL-GROWTH; DNA-DAMAGE; A/C DEFICIENCY; STEM-CELLS; EXTRACELLULAR-MATRIX; BINDING-PROTEIN; RETINOBLASTOMA PROTEIN; TRANSCRIPTION FACTORS;
D O I
10.1016/j.ejcb.2016.06.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Morphological changes in the size and shape of the nucleus are highly prevalent in cancer, but the underlying molecular mechanisms and the functional relevance remain poorly understood. Nuclear envelope proteins, which can modulate nuclear shape and organization, have emerged as key components in a variety of signalling pathways long implicated in tumourigenesis and metastasis. The expression of nuclear envelope proteins is altered in many cancers, and changes in levels of nuclear envelope proteins lamins A and C are associated with poor prognosis in multiple human cancers. In this review we highlight the role of the nuclear envelope in different processes important for tumour initiation and cancer progression, with a focus on lamins A and C. Lamin A/C controls many cellular processes with key roles in cancer, including cell invasion, stemness, genomic stability, signal transduction, transcriptional regulation, and resistance to mechanical stress. In addition, we discuss potential mechanisms mediating the changes in lamin levels observed in many cancers. A better understanding of cause-and-effect relationships between lamin expression and tumour progression could reveal important mechanisms for coordinated regulation of oncogenic processes, and indicate therapeutic vulnerabilities that could be exploited for improved patient outcome. (C) 2016 Elsevier GmbH. All rights reserved.
引用
收藏
页码:449 / 464
页数:16
相关论文
共 233 条
[1]   Human breast cancer invasion and aggression correlates with ECM stiffening and immune cell infiltration [J].
Acerbi, I. ;
Cassereau, L. ;
Dean, I. ;
Shi, Q. ;
Au, A. ;
Park, C. ;
Chen, Y. Y. ;
Liphardt, J. ;
Hwang, E. S. ;
Weaver, V. M. .
INTEGRATIVE BIOLOGY, 2015, 7 (10) :1120-1134
[2]   Inhibition of 12-LOX and COX-2 reduces the proliferation of human epidermoid carcinoma cells (A431) by modulating the ERK and PI3K-Akt signalling pathways [J].
Agarwal, Smita ;
Achari, Chandrani ;
Praveen, D. ;
Roy, Karnati R. ;
Reddy, Gorla Venkateswara ;
Reddanna, Pallu .
EXPERIMENTAL DERMATOLOGY, 2009, 18 (11) :939-946
[3]   Inactivation of the Lamin A/C gene by CpG island promoter hypermethylation in hematologic malignancies, and its association with poor survival in nodal diffuse large B-cell lymphoma [J].
Agrelo, R ;
Setien, F ;
Espada, J ;
Artiga, MJ ;
Rodriguez, M ;
Pérez-Rosado, AP ;
Sanchez-Aguilera, A ;
Fraga, MF ;
Piris, MA ;
Esteller, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (17) :3940-3947
[4]   Differential nuclear remodeling of mammalian somatic cells by Xenopus laevis oocyte and egg cytoplasm [J].
Alberio, R ;
Johnson, AD ;
Stick, R ;
Campbell, KHS .
EXPERIMENTAL CELL RESEARCH, 2005, 307 (01) :131-141
[5]   Altered Lamin A/C splice variant expression as a possible diagnostic marker in breast cancer [J].
Aljada, Ahmad ;
Doria, Joseph ;
Saleh, Ayman M. ;
Al-Matar, Shahad H. ;
AlGabbani, Sarah ;
Shamsa, Heba Bani ;
Al-Bawab, Ahmad ;
Ahmed, Altayeb Abdalla .
CELLULAR ONCOLOGY, 2016, 39 (02) :161-174
[6]   Role of A-type lamins in signaling, transcription, and chromatin organization [J].
Andres, Vicente ;
Gonzalez, Jose M. .
JOURNAL OF CELL BIOLOGY, 2009, 187 (07) :945-957
[7]   Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies [J].
Arimura, T ;
Helbling-Leclerc, A ;
Varnous, S ;
Niel, F ;
Lacène, E ;
Fromes, Y ;
Toussaint, M ;
Mura, AM ;
Keller, DI ;
Amthor, H ;
Isnard, R ;
Malissen, M ;
Schwartz, K ;
Bonne, G .
HUMAN MOLECULAR GENETICS, 2005, 14 (01) :155-169
[8]   Nuclear Actin Network Assembly by Formins Regulates the SRF Coactivator MAL [J].
Baarlink, Christian ;
Wang, Haicui ;
Grosse, Robert .
SCIENCE, 2013, 340 (6134) :864-867
[9]   A proteomic screen identified stress-induced chaperone proteins as targets of Akt phosphorylation in mesangial cells [J].
Barati, Michelle T. ;
Rane, Madhavi J. ;
Klein, Jon B. ;
McLeish, Kenneth R. .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (07) :1636-1646
[10]   Loss of lamin A/C expression in stage II and III colon cancer is associated with disease recurrence [J].
Belt, E. J. Th. ;
Fijneman, R. J. A. ;
van den Berg, E. G. ;
Bril, H. ;
Delis-van Diemen, P. M. ;
Tijssen, M. ;
van Essen, H. F. ;
de lange-de Klerk, E. S. M. ;
Belien, J. A. M. ;
Stockmann, H. B. A. C. ;
Meijer, S. ;
Meijer, G. A. .
EUROPEAN JOURNAL OF CANCER, 2011, 47 (12) :1837-1845