BCL6 gene translocation in follicular lymphoma:: a harbinger of eventual transformation to diffuse aggressive lymphoma

被引:109
作者
Akasaka, T [1 ]
Lossos, IS [1 ]
Levy, R [1 ]
机构
[1] Stanford Univ, Sch Med, Div Oncol, Dept Med, Stanford, CA 94305 USA
关键词
D O I
10.1182/blood-2002-08-2482
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Follicular lymphoma (FL) is characterized by a relatively indolent clinical course, but the disease often transforms into a more aggressive large cell lymphoma with a rapidly progressive clinical course. In the present study, we analyzed 41 cases of FL known to have subsequently transformed to aggressive lymphoma and an additional 64 FL samples from patients not subsequently transformed. We studied BCL6 gene rearrangement by the methodology of long-distance inverse polymerase chain reaction (LDI-PCR). Of the 41 cases known to transform, 16 (39.0%) harbored BCL6 translocation or deletion at the time of FL diagnosis. Among 64 cases not known to transform, BCL6 translocation was detected in 9 (14.1%). The prevalence of BCL6 translocation in the group known to transform was significantly higher (P = .0048). Among the transformation cases, the partners of the BCL6 translocation were identified in 13 cases and included IGH, CIITA, U50HG, MBNL, GRHPR, LRMP, EIF4A2, RhoH/TTF, and LOC92656 (similar to NAPA), whereas in the control group the BCL6 partners were IGH, CIITA, SIAT1, and MBNL. In 13 cases paired specimens before and after transformation available. Among these paired specimens, a loss (3 cases) or a gain (1 case) of BCL6 translocation was observed after the transformation. Analysis of clonality showed that all of these cases represented the evolution of a subclone of the original tumor population. Our study demonstrated that BCL6 translocation is not necessary for transformation but that BCL6 translocation in FL may constitute a subgroup with a higher risk to transform into aggressive lymphoma. (C) 2003 by The American Society of Hematology.
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收藏
页码:1443 / 1448
页数:6
相关论文
共 57 条
[1]   HISTOLOGIC CONVERSION IN THE NON-HODGKINS LYMPHOMAS [J].
ACKER, B ;
HOPPE, RT ;
COLBY, TV ;
COX, RS ;
KAPLAN, HS ;
ROSENBERG, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (01) :11-16
[2]  
Akasaka H, 2000, CANCER RES, V60, P2335
[3]  
Akasaka T, 2000, BLOOD, V96, P2907
[4]  
Akasaka T, 1998, GENE CHROMOSOME CANC, V21, P17, DOI 10.1002/(SICI)1098-2264(199801)21:1<17::AID-GCC4>3.0.CO
[5]  
2-B
[6]   Molecular and clinical features of non-Burkitt's, diffuse large-cell lymphoma of B-cell type associated with the c-MYC/immunoglobulin heavy-chain fusion gene [J].
Akasaka, T ;
Akasaka, H ;
Ueda, C ;
Yonetani, N ;
Maesako, Y ;
Shimizu, A ;
Yamabe, H ;
Fukuhara, S ;
Uchiyama, T ;
Ohno, H .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (03) :510-518
[7]  
Akasaka T, 1996, BLOOD, V88, P985
[8]   p53 mutation in B-cell lymphoid neoplasms with reference to oncogene rearrangements associated with chromosomal translocations [J].
Akasaka, T ;
Muramatsu, M ;
Kadowaki, N ;
Ohno, H ;
Ishizaki, K ;
Yamabe, H ;
Fukuhara, S ;
Okuma, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1996, 87 (09) :930-937
[9]   CORRELATION OF SECONDARY CYTOGENETIC ABNORMALITIES WITH HISTOLOGIC APPEARANCE IN NON-HODGKINS LYMPHOMAS BEARING T(14, 18)(Q32, Q21) [J].
ARMITAGE, JO ;
SANGER, WG ;
WEISENBURGER, DD ;
HARRINGTON, DS ;
LINDER, J ;
BIERMAN, PJ ;
VOSE, JM ;
PURTILO, DT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (08) :576-580
[10]  
BASTARD C, 1994, BLOOD, V83, P2423