• 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

原代 1 蛋白(prox1)在卡波西样血管内皮细胞瘤和丛状血管瘤中的表达。

Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma.

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Am J Surg Pathol. 2010 Nov;34(11):1563-73. doi: 10.1097/PAS.0b013e3181f6076f.

DOI:10.1097/PAS.0b013e3181f6076f
PMID:20975337
Abstract

Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are rare tumors mainly occurring in early childhood. Our recent results showed that ectopic overexpression of human Prox1 gene, a lymphatic endothelial nuclear transcription factor, promoted an aggressive behavior in 2 murine models of KHE. This dramatic Prox1-induced phenotype prompted us to investigate immunohistochemical staining pattern of Prox1, podoplanin (D2-40), LYVE-1, and Prox1/CD34 as well as double immunofluorescent staining pattern of LYVE-1/CD31 in KHE and TA, compared with other pediatric vascular tumors. For this purpose, we examined 75 vascular lesions: KHE (n=18), TA (n=13), infantile hemangioma (n=13), pyogenic granuloma (n=18), and granulation tissue (n=13). Overall, KHE and TA shared an identical endothelial immunophenotype: the neoplastic spindle cells were Prox1, podoplanin, LYVE-1, CD31, and CD34, whereas endothelial cells within glomeruloid foci were Prox1, podoplanin, LYVE-1, CD31, and CD34. The lesional cells of all infantile hemangiomas and pyogenic granulomas were negative for Prox1 in the presence of positive internal control. These findings provide immunophenotypic evidence to support a preexisting notion that KHE and TA are closely related, if not identical. Overall, our results show, for the first time, that Prox1 is an immunohistochemical biomarker helpful in confirming the diagnosis of KHE/TA and in distinguishing it from infantile hemangioma and pyogenic granuloma.

摘要

丛状血管瘤(KHE)和丛状毛细血管瘤(TA)是罕见的肿瘤,主要发生在儿童早期。我们最近的研究结果表明,人 Prox1 基因的异位过表达,一种淋巴管内皮核转录因子,在 2 种 KHE 的小鼠模型中促进了侵袭性行为。Prox1 诱导的这种显著表型促使我们研究了 Prox1、 podoplanin(D2-40)、LYVE-1 和 Prox1/CD34 的免疫组织化学染色模式,以及 KHE 和 TA 中 LYVE-1/CD31 的双免疫荧光染色模式,与其他儿科血管肿瘤进行比较。为此,我们检查了 75 个血管病变:KHE(n=18)、TA(n=13)、婴儿血管瘤(n=13)、化脓性肉芽肿(n=18)和肉芽组织(n=13)。总体而言,KHE 和 TA 具有相同的内皮免疫表型:肿瘤性梭形细胞为 Prox1、podoplanin、LYVE-1、CD31 和 CD34,而肾小球样病灶内的内皮细胞为 Prox1、podoplanin、LYVE-1、CD31 和 CD34。所有婴儿血管瘤和化脓性肉芽肿的病变细胞在存在阳性内部对照的情况下均为 Prox1 阴性。这些发现提供了免疫表型证据,支持 KHE 和 TA 密切相关的观点,如果不是相同的话。总之,我们的研究结果首次表明,Prox1 是一种有助于确认 KHE/TA 诊断并将其与婴儿血管瘤和化脓性肉芽肿区分开来的免疫组织化学标志物。

相似文献

1
Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma.原代 1 蛋白(prox1)在卡波西样血管内皮细胞瘤和丛状血管瘤中的表达。
Am J Surg Pathol. 2010 Nov;34(11):1563-73. doi: 10.1097/PAS.0b013e3181f6076f.
2
Usefulness of D2-40 immunohistochemistry for differentiation between kaposiform hemangioendothelioma and tufted angioma.D2-40免疫组化在鉴别卡波西样血管内皮瘤和簇状血管瘤中的应用价值
J Cutan Pathol. 2006 Jul;33(7):492-7. doi: 10.1111/j.1600-0560.2006.00461.x.
3
The transcription factor Prox1 is a marker for lymphatic endothelial cells in normal and diseased human tissues.转录因子Prox1是正常和患病人体组织中淋巴管内皮细胞的标志物。
FASEB J. 2002 Aug;16(10):1271-3. doi: 10.1096/fj.01-1010fje. Epub 2002 Jun 7.
4
Prox1 transcription factor as a marker for vascular tumors-evaluation of 314 vascular endothelial and 1086 nonvascular tumors.Prox1 转录因子作为血管肿瘤标志物的评估——对 314 例血管内皮肿瘤和 1086 例非血管肿瘤的评估。
Am J Surg Pathol. 2012 Mar;36(3):351-9. doi: 10.1097/PAS.0b013e318236c312.
5
Expression of Prox1, D2-40, and WT1 in spindle cell hemangioma.Prox1、D2-40和WT1在梭形细胞血管瘤中的表达。
J Cutan Pathol. 2014 May;41(5):447-50. doi: 10.1111/cup.12309. Epub 2014 Mar 7.
6
[Vascular tumors and pseudotumors. Kaposiform hemangioendothelioma].[血管肿瘤和假性肿瘤。卡波西样血管内皮瘤]
Ann Pathol. 2011 Aug;31(4):260-5. doi: 10.1016/j.annpat.2011.04.011. Epub 2011 Jul 8.
7
Ultrasonography and magnetic resonance imaging features of kaposiform hemangioendothelioma and tufted angioma.卡波西样血管内皮细胞瘤和丛状血管瘤的超声及磁共振成像特征。
J Dermatol. 2019 Oct;46(10):835-842. doi: 10.1111/1346-8138.15025. Epub 2019 Aug 2.
8
Overexpression Prox1 in HemECs resembles Kaposiform hemangioendothelioma and cytotoxicity of sirolimus in vitro.HemECs 中 Prox1 的过表达类似于卡波西样血管内皮细胞瘤,且体外西罗莫司具有细胞毒性。
J Pediatr Surg. 2021 Jul;56(7):1203-1210. doi: 10.1016/j.jpedsurg.2021.03.023. Epub 2021 Mar 26.
9
Vascular Tumors in Infants: Case Report and Review of Clinical, Histopathologic, and Immunohistochemical Characteristics of Infantile Hemangioma, Pyogenic Granuloma, Noninvoluting Congenital Hemangioma, Tufted Angioma, and Kaposiform Hemangioendothelioma.婴儿血管肿瘤:病例报告及婴儿血管瘤、化脓性肉芽肿、非消退性先天性血管瘤、丛状血管瘤和卡波西样血管内皮瘤的临床、组织病理学及免疫组化特征综述
Am J Dermatopathol. 2018 Apr;40(4):231-239. doi: 10.1097/DAD.0000000000000983.
10
Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon.无卡萨巴-梅里特现象的卡波西样血管内皮瘤
J Am Acad Dermatol. 2005 Apr;52(4):616-22. doi: 10.1016/j.jaad.2004.10.880.

引用本文的文献

1
Rapid Response to Sirolimus in Patients with PIK3CA-Related Overgrowth Spectrum.PIK3CA相关过度生长谱系患者对西罗莫司的快速反应
Eplasty. 2024 Dec 13;24:e66. eCollection 2024.
2
Recent advances in nanomaterial-driven strategies for diagnosis and therapy of vascular anomalies.纳米材料驱动的血管异常诊断和治疗策略的最新进展。
J Nanobiotechnology. 2024 Mar 18;22(1):120. doi: 10.1186/s12951-024-02370-2.
3
Case report: Kaposi hemangioendothelioma of the right upper limb with the Kasabach-Merritt phenomenon: A potentially lethal diagnostic challenge.
病例报告:伴有卡萨巴赫-梅里特现象的右上肢卡波西血管内皮瘤:一项具有潜在致命性的诊断挑战。
Front Pediatr. 2022 Nov 1;10:995399. doi: 10.3389/fped.2022.995399. eCollection 2022.
4
Cerebral Tufted Angioma with Gradually Developing Peritumoral Edema: A Case Report.伴有逐渐发展的瘤周水肿的脑簇状血管瘤:一例报告
NMC Case Rep J. 2022 Jun 21;9:187-192. doi: 10.2176/jns-nmc.2022-0079. eCollection 2022.
5
Malignant Superficial Mesenchymal Tumors in Children.儿童恶性浅表间叶组织肿瘤
Cancers (Basel). 2022 Apr 26;14(9):2160. doi: 10.3390/cancers14092160.
6
Case Report: Cutaneous Pleomorphic Lymphangiosarcoma in a Dog Exhibiting Features of Human Composite Hemangioendothelioma.病例报告:一只表现出人类复合性血管内皮瘤特征的犬皮肤多形性淋巴管肉瘤
Front Vet Sci. 2021 Oct 22;8:666226. doi: 10.3389/fvets.2021.666226. eCollection 2021.
7
Vascular Anomalies of the Head and Neck: A Pediatric Overview.头颈部血管异常:儿科概述。
Head Neck Pathol. 2021 Mar;15(1):59-70. doi: 10.1007/s12105-020-01236-x. Epub 2021 Mar 15.
8
Kaposiform hemangioendothelioma: current knowledge and future perspectives.卡波西样血管内皮细胞瘤:现状与展望。
Orphanet J Rare Dis. 2020 Feb 3;15(1):39. doi: 10.1186/s13023-020-1320-1.
9
A Dusky Red Plaque with Satellite Lesions.一个带有卫星病灶的暗红色斑块。
Indian Dermatol Online J. 2019 Aug 28;10(5):598-600. doi: 10.4103/idoj.IDOJ_152_18. eCollection 2019 Sep-Oct.
10
What is new in endothelial neoplasia?内皮肿瘤有哪些新进展?
Virchows Arch. 2020 Jan;476(1):17-28. doi: 10.1007/s00428-019-02651-4. Epub 2019 Aug 28.