MONOCLONAL-ANTIBODY AGAINST PRAD1/CYCLIN D1 STAINS NUCLEI OF TUMOR-CELLS WITH TRANSLOCATION OR AMPLIFICATION AT BCL-1 LOCUS

被引:57
作者
BANNO, S
YOSHIKAWA, K
NAKAMURA, S
YAMAMOTO, K
SEITO, T
NITTA, M
TAKAHASHI, T
UEDA, R
SETO, M
机构
[1] AICHI CANC CTR, RES INST, CHEMOTHERAPY LAB, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[2] AICHI CANC CTR, RES INST, IMMUNOL LAB, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[3] NAGOYA CITY UNIV, SCH MED, DEPT INTERNAL MED 2, MIZUHO KU, NAGOYA, AICHI 467, JAPAN
[4] AICHI MED UNIV, DEPT PATHOL 2, NAGAKUTE, AICHI 48011, JAPAN
[5] AICHI CANC CTR HOSP, DEPT PATHOL & CLIN LABS, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[6] IMMUNOBIOL LABS CO LTD, NAKA KU, FUJIOKA, GUNMA 375, JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1994年 / 85卷 / 09期
关键词
PRAD1; CYCLIN D1; BCL-1; CHROMOSOMAL TRANSLOCATION; LYMPHOMA;
D O I
10.1111/j.1349-7006.1994.tb02969.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mouse monoclonal antibodies were produced against the bacterial product encoded by human PRAD1/cyclin D1 gene, which is known to be involved in tumors with translocation or amplification at BCL-1 locus of 11q13. The immunizing antigens used were GST-PRAD1 and T7 gene 10-PRAD1 fusion products. Four antibodies were reactive with both PRAD1 fusion products and cell lysates of B-cell tumor cell lines with t(11;14)(q13;q32) and a breast cancer cell line with 11q13 amplification, on immunoblotting. An immunofluorescence study showed that only one of them stained nuclei of cells with 11q13 abnormalities. Since this antibody proved applicable for conventional paraffin-embedded tissue sections, immunohistologic staining of various lymphoma tissues was performed. Eight of 11 mantle cell lymphomas showed intermediate to strong positivity and 6 of the positive cases demonstrated characteristic staining patterns that were either predominantly nuclear or both nuclear and cytoplasmic. The nuclear staining pattern was not observed with other types of lymphoma and thus may correlate with PRAD1 mRNA overexpression.
引用
收藏
页码:918 / 926
页数:9
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