Cyclin D1-negative mantle cell lymphoma:: a clinicopathologic study based on gene expression profiling

被引:240
作者
Fu, K [1 ]
Weisenburger, DD
Greiner, TC
Dave, S
Wright, G
Rosenwald, A
Chiorazzi, M
Iqbal, J
Gesk, S
Siebert, R
De Jong, D
Jaffe, ES
Wilson, WH
Delabie, J
Ott, G
Dave, BJ
Sanger, WG
Smith, LM
Rimsza, L
Braziel, RM
Müller-Hermelink, HK
Campo, E
Gascoyne, RD
Staudt, LM
Chan, WC
机构
[1] Univ Nebraska, Med Ctr, Dept Pathol & Microbiol, Nebraska Med Ctr 983135, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Dept Prevent & Societal Med, Omaha, NE 68198 USA
[3] Univ Nebraska, Med Ctr, Human Genet Lab, Omaha, NE 68198 USA
[4] NCI, Metab Branch, NIH, Bethesda, MD 20892 USA
[5] NCI, Hematopathol Sect, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[6] NCI, Sect Lymphoma Clin Res, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[7] NCI, Biometr Res Branch, Div Canc Treatment & Diag, NIH, Bethesda, MD 20892 USA
[8] Univ Wurzburg, Dept Pathol, D-8700 Wurzburg, Germany
[9] Univ Hosp Schleswig Holstein, Inst Human Genet, Kiel, Germany
[10] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Pathol, Amsterdam, Netherlands
[11] Norwegian Radium Hosp, Dept Pathol, Oslo, Norway
[12] Univ Arizona, Hlth Sci Ctr, Dept Pathol, Tucson, AZ USA
[13] Univ Oregon, Hlth Sci Ctr, Dept Pathol, Portland, OR USA
[14] Univ Barcelona, Hosp Clin, Dept Pathol, Barcelona, Spain
[15] British Columbia Canc Agcy, Dept Pathol, Vancouver, BC V5Z 4E6, Canada
关键词
D O I
10.1182/blood-2005-04-1753
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cyclin D1 overexpression is believed to be essential in the pathogenesis of mantle cell lymphoma (MCL). Hence, the existence of cyclin D1-negative MCL has been controversial and difficult to substantiate. Our previous gene expression profiling study identified several cases that lacked cyclin D1 expression, but had a gene expression signature typical of MCL. Herein, we report the clinical, pathologic, and genetic features of 6 cases of cyclin D1-negative MCL. All 6 cases exhibited the characteristic morphologic features and the unique gene expression signature of MCL but lacked the t(11;14)(q13; q32) by fluorescence in situ hybridization (FISH) analysis. The tumor cells also failed to express cyclin D1 protein, but instead expressed either cyclin D2 (2 cases) or cyclin D3 (4 cases). There was good correlation between cyclin D protein expression and the corresponding mRNA expression levels by gene expression analysis. Using interphase FISH, we did not detect chromosomal translocations or amplifications involving CCND2 and CCND3 loci in these cases. Patients with cyclin D1-negative MCL were similar clinically to those with cyclin D1-positive MCL. In conclusion, cases of cyclin D1-negative MCL do exist and are part of the spectrum of MCL. Up-regulation of cyclin D2 or D3 may substitute for cyclin D1 in the pathogenesis of MCL.
引用
收藏
页码:4315 / 4321
页数:7
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