Combined PER2 and CRY1 expression predicts outcome in chronic lymphocytic leukemia

被引:40
作者
Eisele, Lewin [1 ]
Prinz, Robert [1 ]
Klein-Hitpass, Ludger [2 ]
Nueckel, Holger [1 ]
Lowinski, Kerstin [1 ]
Thomale, Juergen [2 ]
Moeller, Lars C. [3 ]
Duehrsen, Ulrich [1 ]
Duerig, Jan [1 ]
机构
[1] Univ Hosp Essen, Dept Hematol, D-45122 Essen, Germany
[2] Univ Hosp Essen, Inst Cell Biol, D-45122 Essen, Germany
[3] Univ Hosp Essen, Dept Endocrinol, D-45122 Essen, Germany
关键词
B-cell chronic lymphocytic leukemia; prognosis; cryptochrome; 1; period homolog 1 (Drosophila); period homolog 2 (Drosophila); CIRCADIAN CLOCK GENES; B-CELL RECEPTOR; DISEASE PROGRESSION; CD38; EXPRESSION; ZAP-70; METHYLATION; MONONUCLEAR; PHENOTYPE;
D O I
10.1111/j.1600-0609.2009.01287.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The objective of this study was to confirm previous results regarding the differential expression and prognostic significance of the circadian gene CRY1 in chronic lymphocytic leukemia (CLL) patients and its relationship with the expression of other circadian genes and well-established prognostic markers. We also aimed to investigate whether the peripheral circadian machinery may be deregulated in CLL cells. The expression of CRY1, PER1, and PER2 was determined by real-time reverse transcriptase polymerase chain reaction (RT-PCR) in 116 CLL patients. The expression at sequential time points over a 24-h period was measured in six CLL patients and six normal donors. We confirmed the differential expression of CRY1 in ZAP-70<SU+</SU/CD38<SU+</SU and ZAP-70<SU-</SU/CD38<SU-</SU CLL samples. Subgroups formed according to CRY1 expression levels differed significantly in time to treatment. This difference was even more pronounced for subgroups stratified by a CRY1 : PER2 expression ratio and the ratio was an independent prognostic marker in a multivariate model. Furthermore, our data indicate disturbances in the periodic expression of circadian genes in CLL cells. Because of their role in the expression of cell cycle-related and DNA-damage response genes, we suggest that the deregulated expression of circadian genes may be linked to the molecular pathogenesis of CLL.
引用
收藏
页码:320 / 327
页数:8
相关论文
共 30 条
[1]
Clock genes in mammalian peripheral tissues [J].
Balsalobre, A .
CELL AND TISSUE RESEARCH, 2002, 309 (01) :193-199
[2]
Circadian clock genes oscillate in human peripheral blood mononuclear cells [J].
Boivin, DB ;
James, FO ;
Wu, AB ;
Cho-Park, PF ;
Xiong, HB ;
Sun, ZS .
BLOOD, 2003, 102 (12) :4143-4145
[3]
ZAP-70 directly enhances TgM signaling in chronic lymphocytic leukemia [J].
Chen, LG ;
Apgar, J ;
Huynh, L ;
Dicker, F ;
Giago-McGahan, T ;
Rassenti, L ;
Weiss, A ;
Kipps, TJ .
BLOOD, 2005, 105 (05) :2036-2041
[4]
Expression of ZAP-70 is associated with increased B-cell receptor signaling in chronic lymphocytic leukemia [J].
Chen, LG ;
Widhopf, G ;
Huynh, L ;
Rassenti, L ;
Rai, KR ;
Weiss, A ;
Kipps, TJ .
BLOOD, 2002, 100 (13) :4609-4614
[5]
Deregulated expression of the PER1, PER2 and PER3 genes in breast cancers [J].
Chen, ST ;
Choo, KB ;
Hou, MF ;
Yeh, KT ;
Kuo, SJ ;
Chang, JG .
CARCINOGENESIS, 2005, 26 (07) :1241-1246
[6]
National Cancer Institute-sponsored Working Group guidelines for chronic lymphocytic leukemia: Revised guidelines for diagnosis and treatment [J].
Cheson, BD ;
Bennett, JM ;
Grever, M ;
Kay, N ;
Keating, MJ ;
OBrien, S ;
Rai, KR .
BLOOD, 1996, 87 (12) :4990-4997
[7]
Mechanisms of disease: Chronic lymphocytic leukemia [J].
Chiorazzi, N ;
Rai, KR ;
Ferrarini, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (08) :804-815
[8]
The circadian gene Period2 plays an important role in tumor suppression and DNA damage response in vivo [J].
Fu, LN ;
Pelicano, H ;
Liu, JS ;
Huang, P ;
Lee, CC .
CELL, 2002, 111 (01) :41-50
[9]
Circadian expression of clock genes in human peripheral leukocytes [J].
Fukuya, Hiroyuki ;
Emoto, Noriaki ;
Nonaka, Hidemi ;
Yagita, Kazuhiro ;
Okamura, Hitoshi ;
Yokoyama, Mitsuhiro .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 354 (04) :924-928
[10]
The role of circadian regulation in cancer [J].
Gery, S. ;
Koeffler, H. P. .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2007, 72 :459-464