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套细胞淋巴瘤中细胞周期蛋白D1的蛋白表达

Cyclin D1 protein expression in mantle cell lymphoma.

作者信息

Alkan S, Schnitzer B, Thompson J L, Moscinski L C, Ross C W

机构信息

Department of Pathology, University of South Florida, H. Lee Moffitt Cancer Center, Tampa, USA.

出版信息

Ann Oncol. 1995 Jul;6(6):567-70. doi: 10.1093/oxfordjournals.annonc.a059245.

Abstract

BACKGROUND

The t(11;14)(q13;q32) is a chromosomal abnormality usually associated with mantle cell (centrocytic) lymphomas, although it has occasionally been reported in other chronic lymphoproliferative disorders such as chronic lymphocytic leukemia, prolymphocytic leukemia, splenic lymphoma with villous lymphocytes, and multiple myeloma. This abnormality results in the translocation of the bcl-1 oncogene from chromosome 11 to the immunoglobulin heavy chain locus on chromosome 14. The bcl-1 oncogene is a member of the cyclin gene family, and high levels of cyclin D1 mRNA are consistently found in malignant B cell proliferations with t(11;14).

PATIENTS AND METHODS

We examined cyclin D1 protein expression in 33 patients with low grade lymphoproliferative disorders and 2 patients with reactive hyperplasias by Western blot analysis using a polyclonal antibody.

RESULTS

8/11 mantle cell lymphomas, 0/11 chronic lymphocytic leukemias, 0/4 hairy cell leukemias, 0/2 Sezary syndrome, 0/2 monocytoid B-cell lymphomas, 0/3 follicular lymphomas, and 0/2 reactive hyperplasias had overexpression of cyclin D1. Cytogenetic analysis was performed in four cases of mantle cell lymphoma; three of these cases had the t(11;14), one of which was hypotetraploid with two copies of t(11;14). Immunophenotypically, all cases of mantle cell lymphoma and chronic lymphocytic leukemia had coexpression of CD5 and CD20.

CONCLUSION

Mantle cell lymphoma may be difficult to discriminate from chronic lymphocytic leukemia, a more indolent disease, on morphologic and immunophenotypic grounds. Our findings suggest that analysis of cyclin D1 protein expression may be helpful in differentiating mantle cell lymphomas from other low grade lymphoproliferative disorders.

摘要

背景

t(11;14)(q13;q32)是一种染色体异常,通常与套细胞(中心细胞性)淋巴瘤相关,尽管偶尔也有报道见于其他慢性淋巴细胞增殖性疾病,如慢性淋巴细胞白血病、幼淋巴细胞白血病、伴绒毛淋巴细胞的脾淋巴瘤以及多发性骨髓瘤。这种异常导致bcl-1癌基因从11号染色体易位至14号染色体上的免疫球蛋白重链基因座。bcl-1癌基因是细胞周期蛋白基因家族的成员,在伴有t(11;14)的恶性B细胞增殖中始终能检测到高水平的细胞周期蛋白D1 mRNA。

患者和方法

我们使用多克隆抗体通过蛋白质免疫印迹分析检测了33例低度淋巴细胞增殖性疾病患者和2例反应性增生患者的细胞周期蛋白D1蛋白表达。

结果

11例套细胞淋巴瘤中有8例、11例慢性淋巴细胞白血病中有0例、4例毛细胞白血病中有0例、2例Sezary综合征中有0例、2例单核细胞样B细胞淋巴瘤中有0例、3例滤泡性淋巴瘤中有0例以及2例反应性增生中有0例出现细胞周期蛋白D1过表达。对4例套细胞淋巴瘤进行了细胞遗传学分析;其中3例存在t(11;14),其中1例为亚四倍体,有两份t(11;14)拷贝。免疫表型分析显示,所有套细胞淋巴瘤和慢性淋巴细胞白血病病例均同时表达CD5和CD20。

结论

套细胞淋巴瘤在形态学和免疫表型方面可能难以与更惰性的慢性淋巴细胞白血病相鉴别。我们的研究结果表明,分析细胞周期蛋白D1蛋白表达可能有助于将套细胞淋巴瘤与其他低度淋巴细胞增殖性疾病区分开来。

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