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黏膜相关淋巴组织低度B细胞淋巴瘤中18q21.1处断点的分子细胞遗传学描绘

Molecular cytogenetic delineation of the breakpoint at 18q21.1 in low-grade B-cell lymphoma of mucosa-associated lymphoid tissue.

作者信息

Akagi T, Tamura A, Motegi M, Suzuki R, Hosokawa Y, Nakamura S, Morishima Y, Seto M, Taniwaki M

机构信息

Laboratory of Chemotherapy, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

Genes Chromosomes Cancer. 1999 Apr;24(4):315-21.

Abstract

Extranodal malignant non-Hodgkin lymphoma of mucosa-associated lymphoid tissue type (MALT lymphoma) represents a subtype of B-cell lymphoid malignancies with distinct clinicopathological features and is often associated with a favorable prognosis. Recent cytogenetic studies have revealed that t(11;18)(q21;q21) is a characteristic chromosomal aberration in low-grade B-cell MALT-type lymphoma. In the present study, we employed florescence in situ hybridization analysis using contiguous YAC clones mapped to the 18q21.1 region to identify a YAC clone, y789F3, encompassing the breakpoint of t(11;18)(q21;q21) in a MALT lymphoma. PI artificial chromosome (PAC) contigs constructed on this YAC clone were used to analyze the breakpoint region. PAC clone 264m4 was observed on normal chromosome 18 and on der(18), and PAC clone 879n 10 on normal chromosome 18 and on der(II), confirming that the breakpoint is located between these two PAC clones. We also found that a region of approximately 500 kb between the two PAC clones was deleted. These results indicate that the locus between PAC clones 264m4 and 879n 10 at 18q21.1 involved in t(11;18) translocation or associated deletion plays an important role in the development of MALT lymphoma.

摘要

黏膜相关淋巴组织型结外恶性非霍奇金淋巴瘤(MALT淋巴瘤)是B细胞淋巴恶性肿瘤的一种亚型,具有独特的临床病理特征,且通常预后良好。最近的细胞遗传学研究表明,t(11;18)(q21;q21)是低度B细胞MALT型淋巴瘤的特征性染色体畸变。在本研究中,我们使用定位到18q21.1区域的连续酵母人工染色体(YAC)克隆进行荧光原位杂交分析,以鉴定一个包含MALT淋巴瘤中t(11;18)(q21;q21)断点的YAC克隆y789F3。基于该YAC克隆构建的噬菌体人工染色体(PAC)重叠群用于分析断点区域。在正常18号染色体和der(18)上观察到PAC克隆264m4,在正常18号染色体和der(11)上观察到PAC克隆879n10,证实断点位于这两个PAC克隆之间。我们还发现这两个PAC克隆之间大约500 kb的区域缺失。这些结果表明,18q21.1处PAC克隆264m4和879n10之间参与t(11;18)易位或相关缺失的位点在MALT淋巴瘤的发生发展中起重要作用。

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