• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

锁骨下区域结节性筋膜炎一例的细胞遗传学发现

Cytogenetic findings in a case of nodular fasciitis of subclavicular region.

作者信息

Velagaleti Gopalrao V N, Tapper Jill K, Panova Neli E, Miettinen Markku, Gatalica Zoran

机构信息

Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.

出版信息

Cancer Genet Cytogenet. 2003 Mar;141(2):160-3. doi: 10.1016/s0165-4608(02)00725-2.

DOI:10.1016/s0165-4608(02)00725-2
PMID:12606136
Abstract

We report a case of nodular fasciitis with a reciprocal translocation involving both homologues of chromosome 15 [46,XX,t(15;15)(q13;q25)]. This is the third case of nodular fasciitis with involvement of chromosome 15. Two genes that are involved in either wound healing and/or tumorigenesis have been mapped to chromosome 15. One of the genes, the keratinocyte growth factor or fibroblast growth factor 7 (KGF or FGF7) was mapped to the 15q22 region, which was involved in a cytogenetic rearrangement in one case of nodular fasciitis. KGF is implicated in wound healing, healing lung injuries and tumorigenesis of various cancers such as breast and prostate. The second gene involved is TRKC or NTRK3 mapped to the 15q25 region. TRKC is implicated in congenital fibrosarcoma, a benign proliferation of fibroblasts. The breakpoint and overexpression of the protein in our case further suggest a possible involvement of TRKC.

摘要

我们报告了一例伴有涉及15号染色体两条同源染色体的相互易位的结节性筋膜炎病例[46,XX,t(15;15)(q13;q25)]。这是第三例涉及15号染色体的结节性筋膜炎病例。两个与伤口愈合和/或肿瘤发生相关的基因已被定位到15号染色体。其中一个基因,即角质形成细胞生长因子或成纤维细胞生长因子7(KGF或FGF7)被定位到15q22区域,在一例结节性筋膜炎中该区域发生了细胞遗传学重排。KGF与伤口愈合、肺损伤修复以及乳腺癌和前列腺癌等多种癌症的肿瘤发生有关。另一个相关基因是TRKC或NTRK3,定位于15q25区域。TRKC与先天性纤维肉瘤有关,后者是成纤维细胞的良性增殖。我们病例中该蛋白的断点和过表达进一步提示TRKC可能参与其中。

相似文献

1
Cytogenetic findings in a case of nodular fasciitis of subclavicular region.锁骨下区域结节性筋膜炎一例的细胞遗传学发现
Cancer Genet Cytogenet. 2003 Mar;141(2):160-3. doi: 10.1016/s0165-4608(02)00725-2.
2
Clonal rearrangement of 15p11.2, 16p11.2, and 16p13.3 in a case of nodular fasciitis: additional evidence favoring nodular fasciitis as a benign neoplasm and not a reactive tumefaction.
Cancer Genet Cytogenet. 2002 Dec;139(2):138-40. doi: 10.1016/s0165-4608(02)00613-1.
3
Involvement of 3q21 in nodular fasciitis.3q21在结节性筋膜炎中的作用。
Cancer Genet Cytogenet. 1998 Oct 15;106(2):177-9. doi: 10.1016/s0165-4608(98)00066-1.
4
A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma.先天性纤维肉瘤中的一种新型ETV6-NTRK3基因融合
Nat Genet. 1998 Feb;18(2):184-7. doi: 10.1038/ng0298-184.
5
Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma.先天性中胚层肾瘤t(12;15)与ETV6-NTRK3基因融合相关:与先天性(婴儿型)纤维肉瘤的细胞遗传学及分子关系
Am J Pathol. 1998 Nov;153(5):1451-8. doi: 10.1016/S0002-9440(10)65732-X.
6
The detection of Tel-TrkC chimeric transcripts is more specific than TrkC immunoreactivity for the diagnosis of congenital fibrosarcoma.对于先天性纤维肉瘤的诊断,检测Tel-TrkC嵌合转录本比TrkC免疫反应性更具特异性。
J Pathol. 2001 Jan;193(1):88-94. doi: 10.1002/1096-9896(2000)9999:9999<::AID-PATH724>3.0.CO;2-S.
7
FGF7-like gene is associated with pericentric inversion of chromosome 9, and FGF7 is involved in the development of ovarian cancer.成纤维细胞生长因子7样基因与9号染色体臂间倒位相关,而成纤维细胞生长因子7参与卵巢癌的发展。
Int J Oncol. 2005 May;26(5):1209-16.
8
Congenital fibrosarcoma with a novel complex 3-way translocation t(12;15;19) and unusual histologic features.伴有新型复杂三向易位t(12;15;19)及不寻常组织学特征的先天性纤维肉瘤
Hum Pathol. 2008 Dec;39(12):1844-8. doi: 10.1016/j.humpath.2008.04.013. Epub 2008 Jul 25.
9
Congenital-infantile fibrosarcoma. A clinicopathologic study of 10 cases and molecular detection of the ETV6-NTRK3 fusion transcripts using paraffin-embedded tissues.先天性婴儿纤维肉瘤:10例临床病理研究及应用石蜡包埋组织对ETV6-NTRK3融合转录本进行分子检测
Am J Clin Pathol. 2001 Mar;115(3):348-55. doi: 10.1309/3H24-E7T7-V37G-AKKQ.
10
Clonal chromosome aberrations in a case of nodular fasciitis.
Cancer Genet Cytogenet. 1994 Sep;76(2):154-6. doi: 10.1016/0165-4608(94)90469-3.

引用本文的文献

1
Fibroma of Tendon Sheath Revisited.腱鞘纤维瘤再探讨。
In Vivo. 2025 Mar-Apr;39(2):613-620. doi: 10.21873/invivo.13866.
2
Ubiquitin-specific Peptidase 6 ()-associated Fibroblastic/Myofibroblastic Tumors: Evolving Concepts.泛素特异性肽酶 6 () 相关的纤维母细胞/肌纤维母细胞瘤:不断发展的概念。
Cancer Genomics Proteomics. 2021 Mar-Apr;18(2):93-101. doi: 10.21873/cgp.20244.
3
The Rare Benign Lesion That Mimics a Malignant Tumor in Breast Parenchyma: Nodular Fasciitis of the Breast.乳腺实质中酷似恶性肿瘤的罕见良性病变:乳腺结节性筋膜炎
Case Rep Pathol. 2018 Apr 30;2018:1612587. doi: 10.1155/2018/1612587. eCollection 2018.
4
Description of a Rare Case of Nodular Fasciitis of the Apical Aspect of the Upper Buccal Sulcus.上颊沟顶端结节性筋膜炎一例罕见病例描述
Case Rep Dent. 2016;2016:4231683. doi: 10.1155/2016/4231683. Epub 2016 Mar 15.
5
Myofibroma in the palm presenting with median nerve compression symptoms.手掌部肌纤维瘤伴正中神经受压症状。
Plast Reconstr Surg Glob Open. 2014 Sep 8;2(8):e204. doi: 10.1097/GOX.0000000000000153. eCollection 2014 Aug.
6
Updates on the cytogenetics and molecular cytogenetics of benign and intermediate soft tissue tumors.良性和中间型软组织肿瘤的细胞遗传学及分子细胞遗传学进展
Oncol Lett. 2013 Jan;5(1):12-18. doi: 10.3892/ol.2012.1002. Epub 2012 Oct 30.
7
[Intramuscular nodular fasciitis--a clinicopathological study with emphasis on myogenic giant cells].[肌内结节性筋膜炎——一项着重于肌源性巨细胞的临床病理研究]
Pathologe. 2006 May;27(3):198-203. doi: 10.1007/s00292-005-0798-6.
8
Bizarre parosteal osteochondromatous proliferation with a t(1;17) translocation.伴有t(1;17)易位的怪异型骨旁骨软骨瘤样增生。
Virchows Arch. 2005 Jul;447(1):99-102. doi: 10.1007/s00428-005-1266-7. Epub 2005 May 31.
9
Multi-lineage interrogation of the performance characteristics of a split-signal fluorescence in situ hybridization probe for anaplastic lymphoma kinase gene rearrangements: a study of 101 cases characterized by immunohistomorphology on fixed archival tissue.用于间变性淋巴瘤激酶基因重排的分裂信号荧光原位杂交探针性能特征的多谱系研究:一项对101例经固定存档组织免疫组织形态学特征分析的病例研究
Mol Diagn. 2004;8(4):213-29. doi: 10.1007/BF03260066.