Alterations of gene expression in blood cells associated with chronic fatigue in breast cancer survivors

被引:40
作者
Landmark-Hoyvik, H. [1 ,2 ]
Reinertsen, K. V. [3 ,4 ]
Loge, J. H. [3 ]
Fossa, S. D. [3 ]
Borresen-Dale, A. L. [1 ,2 ]
Dumeaux, V. [1 ,5 ]
机构
[1] Oslo Univ Hosp, Dept Genet, Inst Canc Res, Norwegian Radium Hosp, N-310 Oslo, Norway
[2] Univ Oslo, Fac Div, Fac Med, Norwegian Radium Hosp, Oslo, Norway
[3] Oslo Univ Hosp, Dept Clin Canc Res, Norwegian Radium Hosp, N-310 Oslo, Norway
[4] Ullevaal Univ Hosp, Canc Dept, Oslo, Norway
[5] Univ Tromso, Inst Community Med, Tromso, Norway
关键词
whole blood; fatigue; breast cancer; gene expression; B cells; QUALITY-OF-LIFE; APOPTOSIS; STRESS; IMPACT;
D O I
10.1038/tpj.2009.27
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fatigue is one of the most frequent complaints among breast cancer survivors. However, mechanisms underlying persisting fatigue after end of treatment are poorly understood. To explore whether biological processes underlying persistent fatigue can affect gene expression of blood cells, genome-wide expression analyses were performed on whole blood samples from breast cancer survivors classified as chronic fatigued 2-6 years after diagnosis. Non-fatigued survivors served as controls. Several gene sets involved in plasma-and B-cell pathways differed between the chronic fatigued and the non-fatigued, suggesting that a dysregulation in these pathways is associated with chronic fatigue and that a B-cell-mediated inflammatory process might underlie fatigue. The chronic fatigued also had a higher level of leucocytes, lymphocytes and neutrophiles compared with the non-fatigued, thus further indicating that an activation of the immune system plays a role in the biology of chronic fatigue in breast cancer survivors. The Pharmacogenomics Journal (2009) 9, 333-340; doi:10.1038/tpj.2009.27; published online 23 June 2009
引用
收藏
页码:333 / 340
页数:8
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