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7q22 易位确定了子宫平滑肌瘤中的一个关键区域。

Translocations in 7q22 define a critical region in uterine leiomyomata.

作者信息

Sargent M S, Weremowicz S, Rein M S, Morton C C

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115.

出版信息

Cancer Genet Cytogenet. 1994 Oct;77(1):65-8. doi: 10.1016/0165-4608(94)90151-1.

DOI:10.1016/0165-4608(94)90151-1
PMID:7923086
Abstract

Rearrangements involving the long arm of chromosome 7 in uterine leiomyoma are widely recognized and comprise one of the major cytogenetic subgroups of these tumors. To approach a molecular genetic investigation of this subgroup for identification of a gene(s) involved in the biology of uterine leiomyomata we have analyzed breakpoints in the del(7q) subgroup in a series of myomas karyotyped in our laboratory. Herein we report the cytogenetic analysis of 11 uterine leiomyomata: eight with interstitial deletions in the long arm of chromosome 7 and three with translocations in 7q. These translocations provide further support for 7q22 as the critical band in the del(7q) subgroup.

摘要

子宫平滑肌瘤中涉及7号染色体长臂的重排已得到广泛认可,并且是这些肿瘤主要的细胞遗传学亚组之一。为了对该亚组进行分子遗传学研究,以鉴定参与子宫平滑肌瘤生物学过程的基因,我们分析了在我们实验室进行核型分析的一系列肌瘤中del(7q)亚组的断点。在此,我们报告11例子宫平滑肌瘤的细胞遗传学分析结果:8例为7号染色体长臂的间质缺失,3例为7q的易位。这些易位进一步支持7q22作为del(7q)亚组中的关键带。

相似文献

1
Translocations in 7q22 define a critical region in uterine leiomyomata.7q22 易位确定了子宫平滑肌瘤中的一个关键区域。
Cancer Genet Cytogenet. 1994 Oct;77(1):65-8. doi: 10.1016/0165-4608(94)90151-1.
2
The del(7q) subgroup in uterine leiomyomata: genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomata.子宫平滑肌瘤中的del(7q)亚组:遗传和生物学特征。子宫平滑肌瘤病理生物学中细胞遗传学异常继发性本质的进一步证据。
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Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis.采用配对分析鉴定子宫平滑肌瘤间质7q缺失亚组的分子特征。
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Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas.44例子宫平滑肌瘤中存在特征性染色体异常,包括6p重排、7q缺失、+12和t(12;14) 。
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Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines.两个子宫平滑肌瘤来源细胞系中7号染色体长臂缺失(del(7q))的分子细胞遗传学特征
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Deletion 7q in uterine leiomyoma: fluorescence in situ hybridization characterization on primary cytogenetic preparations.子宫平滑肌瘤中的7号染色体长臂缺失:原代细胞遗传学标本的荧光原位杂交特征分析
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Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).通过荧光原位杂交(FISH)对7号染色体长臂(7q)缺失进行分类并鉴定隐匿性易位。
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引用本文的文献

1
A View on Uterine Leiomyoma Genesis through the Prism of Genetic, Epigenetic and Cellular Heterogeneity.从遗传、表观遗传和细胞异质性的角度看子宫肌瘤的发生。
Int J Mol Sci. 2023 Mar 17;24(6):5752. doi: 10.3390/ijms24065752.
2
Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis.采用配对分析鉴定子宫平滑肌瘤间质7q缺失亚组的分子特征。
Genes Chromosomes Cancer. 2009 Oct;48(10):865-85. doi: 10.1002/gcc.20692.
3
Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids.
丛状平滑肌瘤的分子和细胞遗传学特征为子宫肌瘤潜在的遗传异质性提供了进一步证据。
Am J Pathol. 2008 May;172(5):1403-10. doi: 10.2353/ajpath.2008.071102. Epub 2008 Apr 10.
4
Disseminated peritoneal leiomyomatosis. Clonality analysis by X chromosome inactivation and cytogenetics of a clinically benign smooth muscle proliferation.播散性腹膜平滑肌瘤病。通过X染色体失活和细胞遗传学对临床良性平滑肌增殖进行克隆性分析。
Am J Pathol. 1997 Jun;150(6):2153-66.
5
HMGI(Y) expression in human uterine leiomyomata. Involvement of another high-mobility group architectural factor in a benign neoplasm.人子宫平滑肌瘤中HMGI(Y)的表达。另一种高迁移率族结构因子参与良性肿瘤的发生。
Am J Pathol. 1997 Mar;150(3):911-8.