共 233 条
Causes and consequences of nuclear envelope alterations in tumour progression
被引:78
作者:

Bell, Emily S.
论文数: 0 引用数: 0
h-index: 0
机构: Cornell Univ, Meinig Sch Biomed Engn, Ithaca, NY 14853 USA

Lammerding, Jan
论文数: 0 引用数: 0
h-index: 0
机构: Cornell Univ, Meinig Sch Biomed Engn, Ithaca, NY 14853 USA
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.
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收藏
页码:449 / 464
页数:16
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