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12号染色体短臂遗传物质的缺失是非霍奇金淋巴瘤常见的继发性异常。

Loss of genetic material from the short arm of chromosome 12 is a frequent secondary abnormality in non-Hodgkin's lymphoma.

作者信息

Jonveaux P, Le Coniat M, Derré J, Vecchione D, Berger R

机构信息

Unité INSERM U 301, Institut de Génétique Moléculaire, Paris, France.

出版信息

Hematol Pathol. 1991;5(1):21-6.

PMID:2050601
Abstract

Abnormalities of the short arm of chromosome 12 have been detected in a wide variety of hematopoietic disorders. Seven cases of non-Hodgkin's lymphoma (NHL) are reported with various rearrangements involving bands 12p13 or 12p11, associated with other chromosome changes. A review of the literature confirms that rearrangements of 12p, mainly at band 12p13, are nonrandom chromosomal abnormalities in all subtypes of NHL, as in other malignant blood disorders. No common translocation could, however, be detected, and 12p abnormalities may be considered as secondary chromosomal events. Most of the 12p rearrangements involving translocation of genetic material of unknown origin, suggest that they result in loss of 12p segment.

摘要

在多种造血系统疾病中均检测到了12号染色体短臂异常。本文报告了7例非霍奇金淋巴瘤(NHL),这些病例存在涉及12p13或12p11带的各种重排,并伴有其他染色体改变。文献综述证实,与其他恶性血液疾病一样,12p重排(主要在12p13带)是NHL所有亚型中的非随机染色体异常。然而,未检测到常见的易位,12p异常可能被视为继发性染色体事件。大多数涉及未知来源遗传物质易位的12p重排表明,它们会导致12p片段缺失。

相似文献

1
Loss of genetic material from the short arm of chromosome 12 is a frequent secondary abnormality in non-Hodgkin's lymphoma.12号染色体短臂遗传物质的缺失是非霍奇金淋巴瘤常见的继发性异常。
Hematol Pathol. 1991;5(1):21-6.
2
FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.荧光原位杂交(FISH)可识别不同类型的重复,其中12q13 - 15是B细胞淋巴增殖性恶性肿瘤中常见的受累片段,这些肿瘤的特征为12号染色体部分三体。
Genes Chromosomes Cancer. 1997 Oct;20(2):155-66.
3
Codeletion of CDKN2 and MTAP genes in a subset of non-Hodgkin's lymphoma may be associated with histologic transformation from low-grade to diffuse large-cell lymphoma.非霍奇金淋巴瘤的一个亚组中CDKN2和MTAP基因的共缺失可能与从低级别向弥漫性大细胞淋巴瘤的组织学转化有关。
Genes Chromosomes Cancer. 1998 May;22(1):72-8.
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Involvement of BCL6 in chromosomal aberrations affecting band 3q27 in B-cell non-Hodgkin lymphoma.BCL6在影响B细胞非霍奇金淋巴瘤中3q27带的染色体畸变中的作用。
Genes Chromosomes Cancer. 1998 Dec;23(4):323-7.
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Loss of chromosome 11q21-23.1 and 17p and gain of chromosome 6p are independent prognostic indicators in B-cell non-Hodgkin's lymphoma.11号染色体q21 - 23.1区域和17号染色体短臂缺失以及6号染色体短臂增加是B细胞非霍奇金淋巴瘤的独立预后指标。
Br J Cancer. 2001 Dec 14;85(12):1900-13. doi: 10.1054/bjoc.2001.2164.
6
The t(11;18)(q21;q21) chromosome translocation is a frequent and specific aberration in low-grade but not high-grade malignant non-Hodgkin's lymphomas of the mucosa-associated lymphoid tissue (MALT-) type.t(11;18)(q21;q21)染色体易位是黏膜相关淋巴组织(MALT-)型低度恶性而非高度恶性非霍奇金淋巴瘤中常见且特异的畸变。
Cancer Res. 1997 Sep 15;57(18):3944-8.
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Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma.B细胞非霍奇金淋巴瘤中13号染色体长臂上常见缺失区域的描绘。
Int J Hematol. 2000 Feb;71(2):159-66.
8
Nonrandom rearrangement of chromosome 14 at band q32.33 in human lymphoid malignancies with mature B-cell phenotype.在具有成熟B细胞表型的人类淋巴恶性肿瘤中,14号染色体q32.33带处的非随机重排。
Cancer Res. 1989 Mar 1;49(5):1275-81.
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Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.非霍奇金淋巴瘤中1p36染色体带的重排
Clin Cancer Res. 1999 Jun;5(6):1401-9.
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Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma.非霍奇金淋巴瘤的染色体异常与分子遗传学
Semin Oncol. 1998 Aug;25(4):447-60.

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