API2-MALT1 chimeric transcripts involved in mucosa-associated lymphoid tissue type lymphoma predict heterogeneous products

被引:100
作者
Motegi, M
Yonezumi, M
Suzuki, H
Suzuki, R
Hosokawa, Y
Hosaka, S
Kodera, Y
Morishima, Y
Nakamura, S
Seto, M
机构
[1] Aichi Canc Ctr, Res Inst, Lab Chemotherapy, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Aichi Canc Ctr Hosp, Dept Hematol & Chemotherapy, Nagoya, Aichi 464, Japan
[3] Aichi Canc Ctr Hosp, Dept Pathol & Clin Labs, Nagoya, Aichi 464, Japan
[4] Shinshu Univ, Sch Med, Dept Internal Med 2, Nagano, Japan
[5] Japanese Red Cross Nagoya First Hosp, Dept Hematol, Nagoya, Aichi, Japan
关键词
D O I
10.1016/S0002-9440(10)64948-6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Recent progress in molecular analysis of low-grade B cell lymphoma has revealed that API2 at 11q21 and a novel gene, MALT1 at 18q21, are involved in t(11;18)(q21;q21), a characteristic chromosome aberration for mucosa-associated lymphoid tissue (MALT) type lymphoma. We describe here the establishment of a reverse transcription-polymerase chain reaction (RT-PCR) assay that me used to analyze 22 cases of MALT lymphoma. All five cases that were shown to possess t(11;18)(q21;q21) showed the specific amplification of API2-MALT1 chimeric transcripts. Of the remaining 17 cases for which cytogenetic data mere not available, three cases demonstrated the presence of fusion transcripts, indicating that a significant percentage of MALT lymphoma cases of the present series appeared to possess t(11;18). A single fragment was observed in each of these cases, but the size varied from case to case. Sequencing analysis revealed that there are two breakpoints in API2 and three in MALT1, and that all of the fusion transcripts are in-frame. On the basis of these results, four kinds of chimeric proteins can be predicted for the present series. Thus, the RT-PCR assay used here should serve as an effective molecular tool for understanding molecular pathogenesis and the clinical significance of API2-MALT1 for MALT lymphomas.
引用
收藏
页码:807 / 812
页数:6
相关论文
共 26 条
[1]  
Akagi T, 1999, GENE CHROMOSOME CANC, V24, P315
[2]   A novel gene, MALT1 at 18q21, is involved in t(11;18) (q21;q21) found in low-grade B-cell lymphoma of mucosa-associated lymphoid tissue [J].
Akagi, T ;
Motegi, M ;
Tamura, A ;
Suzuki, R ;
Hosokawa, Y ;
Suzuki, H ;
Ota, H ;
Nakamura, S ;
Morishima, Y ;
Taniwaki, M ;
Seto, M .
ONCOGENE, 1999, 18 (42) :5785-5794
[3]   AN APOPTOSIS-INHIBITING GENE FROM A NUCLEAR POLYHEDROSIS-VIRUS ENCODING A POLYPEPTIDE WITH CYS/HIS SEQUENCE MOTIF [J].
BIRNBAUM, MJ ;
CLEM, RJ ;
MILLER, LK .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2521-2528
[4]  
Brynes RK, 1996, MODERN PATHOL, V9, P995
[5]  
CROCE CM, 1993, SEMIN ONCOL, V20, P31
[6]   HUMAN C-MYC ONC GENE IS LOCATED ON THE REGION OF CHROMOSOME-8 THAT IS TRANSLOCATED IN BURKITT-LYMPHOMA CELLS [J].
DALLAFAVERA, R ;
BREGNI, M ;
ERIKSON, J ;
PATTERSON, D ;
GALLO, RC ;
CROCE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (24) :7824-7827
[7]   The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas [J].
Dierlamm, J ;
Baens, M ;
Wlodarska, I ;
Stefanova-Ouzounova, M ;
Hernandez, JM ;
Hossfeld, DK ;
De Wolf-Peeters, C ;
Hagemeijer, A ;
Van den Berghe, H ;
Marynen, P .
BLOOD, 1999, 93 (11) :3601-3609
[8]   TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION [J].
DON, RH ;
COX, PT ;
WAINWRIGHT, BJ ;
BAKER, K ;
MATTICK, JS .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :4008-4008
[9]  
Greiner A, 1997, AM J PATHOL, V150, P1583
[10]  
HARRIS NL, 1994, BLOOD, V84, P1361