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Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease.

作者信息

Dal Cin P, De Smet L, Sciot R, Van Damme B, Van den Berghe H

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Cancer Genet Cytogenet. 1999 Jan 15;108(2):137-40. doi: 10.1016/s0165-4608(98)00126-5.

DOI:10.1016/s0165-4608(98)00126-5
PMID:9973941
Abstract

Cytogenetic and molecular cytogenetic analysis is reported in a series of 40 tissue samples from 36 patients with Dupuytren's disease, presenting as palmar and/or finger nodules. No consistent structural chromosome changes could be found. Instead, recurrent clonal numerical abnormalities were demonstrated in 22 of 40 tissue nodules, involving trisomies of chromosome 7 or 8 and loss of the Y chromosome. In addition, we showed that trisomy 7 and trisomy 8 were also present in non-dividing cells.

摘要

相似文献

1
Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease.
Cancer Genet Cytogenet. 1999 Jan 15;108(2):137-40. doi: 10.1016/s0165-4608(98)00126-5.
2
Cytogenetic and interphase cytogenetic analyses reveal chromosome instability but no clonal trisomy 8 in Dupuytren contracture.细胞遗传学和间期细胞遗传学分析显示,掌腱膜挛缩存在染色体不稳定,但不存在克隆性8号染色体三体。
Cancer Genet Cytogenet. 1997 Nov;99(1):73-6. doi: 10.1016/s0165-4608(96)00430-x.
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Chromosomal abnormalities in Dupuytren's contracture and carpal tunnel syndrome.掌腱膜挛缩症和腕管综合征中的染色体异常。
J Hand Surg Br. 1992 Jun;17(3):349-55. doi: 10.1016/0266-7681(92)90128-o.
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DNA copy number variations at chromosome 7p14.1 and chromosome 14q11.2 are associated with dupuytren's disease: potential role for MMP and Wnt signaling pathway.染色体 7p14.1 和染色体 14q11.2 上的 DNA 拷贝数变异与掌腱膜挛缩症相关:MMP 和 Wnt 信号通路的潜在作用。
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Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis.所谓杜普伊特伦氏甲下外生骨疣中的克隆性染色体异常。
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Is Dupuytren's disease caused by an imbalance between proliferation and cell death?掌腱膜挛缩症是由增殖与细胞死亡之间的失衡引起的吗?
J Hand Surg Br. 1999 Oct;24(5):511-4. doi: 10.1054/jhsb.1999.0251.
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Chromosome abnormalities in Dupuytren's disease.
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Trisomy 8 and 18 as frequent clonal and single-cell aberrations in 185 primary breast carcinomas.8号和18号染色体三体作为185例原发性乳腺癌中常见的克隆性和单细胞畸变。
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No gene copy number changes in Dupuytren's contracture by array comparative genomic hybridization.通过阵列比较基因组杂交技术未发现杜普伊特伦挛缩症存在基因拷贝数变化。
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J Hand Surg Br. 2002 Jun;27(3):270-3. doi: 10.1054/jhsb.2001.0742.

引用本文的文献

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Peyronie's disease: is it genetic or not?佩罗尼氏病:它有遗传性吗?
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PEYRONIE'S DISEASE: A REVIEW OF ETIOLOGY, DIAGNOSIS, AND MANAGEMENT.佩罗尼氏病:病因、诊断与治疗综述
Curr Sex Health Rep. 2015 Jun 1;7(2):117-131. doi: 10.1007/s11930-015-0045-y.
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Aggressive Dupuytren's diathesis in a young woman.一名年轻女性的侵袭性掌腱膜挛缩素质
BMJ Case Rep. 2010 Sep 20;2010:bcr1220092592. doi: 10.1136/bcr.12.2009.2592.
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Scientific understanding and clinical management of Dupuytren disease.Dupuytren 病的科学认识和临床管理。
Nat Rev Rheumatol. 2010 Dec;6(12):715-26. doi: 10.1038/nrrheum.2010.180. Epub 2010 Nov 9.
6
Elevated levels of beta-catenin and fibronectin in three-dimensional collagen cultures of Dupuytren's disease cells are regulated by tension in vitro.掌腱膜挛缩症细胞三维胶原培养物中β-连环蛋白和纤连蛋白水平的升高在体外受张力调节。
BMC Musculoskelet Disord. 2003 Jul 16;4:16. doi: 10.1186/1471-2474-4-16.
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Clonal chromosomal abnormality induced by surgically retained foreign bodies: t(9;17)(q21;p13.3) in a textiloma.手术残留异物诱导的克隆性染色体异常:纺织瘤中的t(9;17)(q21;p13.3)
Virchows Arch. 2003 May;442(5):507-8. doi: 10.1007/s00428-003-0792-4. Epub 2003 Apr 12.
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Trisomies 8 and 20 characterize a subgroup of benign fibrous lesions arising in both soft tissue and bone.8号和20号染色体三体是软组织和骨骼中出现的一组良性纤维性病变的特征。
Am J Pathol. 1999 Mar;154(3):729-33. doi: 10.1016/S0002-9440(10)65319-9.