Circadian disruption and breast cancer: An epigenetic link?

被引:27
作者
Kochan, David Z. [1 ]
Kovalchuk, Olga [1 ]
机构
[1] Univ Lethbridge, Dept Biol Sci, Lethbridge, AB T1K 3M4, Canada
关键词
breast cancer; circadian disruption (CD); epigenetics; circadian rhythms; melatonin (MLT); ESTROGEN-RECEPTOR-ALPHA; LONG-TERM SHIFTWORK; DNA METHYLATION; SUPRACHIASMATIC NUCLEUS; TUMOR-SUPPRESSOR; GENE-EXPRESSION; CELL-GROWTH; ER-ALPHA; MELATONIN; LIGHT;
D O I
10.18632/oncotarget.4343
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is already the most common malignancy affecting women worldwide, and evidence is mounting that breast cancer induced by circadian disruption ( CD) is a warranted concern. Numerous studies have investigated various aspects of the circadian clock in relation to breast cancer, and evidence from these studies indicates that melatonin and the core clock genes can play a crucial role in breast cancer development. Even though epigenetics has been increasingly recognized as a key player in the etiology of breast cancer and linked to circadian rhythms, and there is evidence of overlap between epigenetic deregulation and breast cancer induced by circadian disruption, only a handful of studies have directly investigated the role of epigenetics in CD-induced breast cancer. This review explores the circadian clock and breast cancer, and the growing role of epigenetics in breast cancer development and circadian rhythms. We also summarize the current knowledge and next steps for the investigation of the epigenetic link in CD-induced breast cancer.
引用
收藏
页码:16866 / 16882
页数:17
相关论文
共 157 条
[71]   The basics of epithelial-mesenchymal transition [J].
Kalluri, Raghu ;
Weinberg, Robert A. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (06) :1420-1428
[72]  
Khvorova A, 2003, CELL, V115, P209, DOI 10.1016/S0092-8674(03)00801-8
[73]   Mouse models for breast cancer metastasis [J].
Kim, Ik Soo ;
Baek, Sung Hee .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 394 (03) :443-447
[74]   Long interspersed nuclear element-1 hypomethylation in cancer: biology and clinical applications [J].
Kitkumthorn, Nakarin ;
Mutirangura, Apiwat .
CLINICAL EPIGENETICS, 2011, 2 :315-330
[75]   Genomic DNA methylation: the mark and its mediators [J].
Klose, RJ ;
Bird, AP .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (02) :89-97
[76]   Breast cancer among shift workers: results of the WOLF longitudinal cohort study [J].
Knutsson, Anders ;
Alfredsson, Lars ;
Karlsson, Berndt ;
Akerstedt, Torbjorn ;
Fransson, Eleonor I. ;
Westerholm, Peter ;
Westerlund, Hugo .
SCANDINAVIAN JOURNAL OF WORK ENVIRONMENT & HEALTH, 2013, 39 (02) :170-177
[77]   Molecular components of the mammalian circadian clock [J].
Ko, Caroline H. ;
Takahashi, Joseph S. .
HUMAN MOLECULAR GENETICS, 2006, 15 :R271-R277
[78]   Role of melatonin in metabolic regulation [J].
Korkmaz, Ahmet ;
Topal, Turgut ;
Tan, Dun-Xian ;
Reiter, Russel J. .
REVIEWS IN ENDOCRINE & METABOLIC DISORDERS, 2009, 10 (04) :261-270
[79]   Combination of melatonin and tamoxifen as a chemoprophylaxis against N-nitroso-N-methylurea-induced rat mammary tumors [J].
Kothari, A ;
Borges, A ;
Ingle, A ;
Kothari, L .
CANCER LETTERS, 1997, 111 (1-2) :59-66
[80]   Small molecules with big effects: The role of the microRNAome in cancer and carcinogenesis [J].
Koturbash, Igor ;
Zemp, Franz J. ;
Pogribny, Igor ;
Kovalchuk, Olga .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2011, 722 (02) :94-105