• 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

BRAFV600E 突变始终存在,并与 Erdheim-Chester 病中的癌基因诱导衰老相关。

BRAFV600E-mutation is invariably present and associated to oncogene-induced senescence in Erdheim-Chester disease.

机构信息

Unit of Pathology, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Vita-Salute San Raffaele University, Milan, Italy.

出版信息

Ann Rheum Dis. 2015 Aug;74(8):1596-602. doi: 10.1136/annrheumdis-2013-204924. Epub 2014 Mar 26.

DOI:10.1136/annrheumdis-2013-204924
PMID:24671772
Abstract

OBJECTIVES

Erdheim-Chester disease (ECD) is a rare form of histiocytosis characterised by uncontrolled chronic inflammation. The oncogenic BRAF(V600E) mutation has been reported in biopsies in 19 out of 37 patients with ECD from the largest published cohort, but never found in the patients' peripheral blood. Also, the role of the mutation in the pathogenesis of the disease has not been elucidated yet. BRAF(V600E) has been associated with oncogene-induced senescence (OIS), a protective mechanism against oncogenic events, characterised by the induction of proinflammatory pathways.

METHODS

We verified the BRAF status in biopsies and peripheral blood from 18 patients with ECD from our cohort and matched controls by means of immunohistochemistry and of an ultrasensitive assay, based on the combination of a locked nucleic acid PCR and pyrosequencing. Droplet digital PCR was used to confirm the findings. We also evaluated the presence of senescence markers in ECD histiocytes.

RESULTS

BRAF(V600E) mutation was present in all the biopsy and peripheral blood samples from patients with ECD and in none of the controls. ECD histiocytes and a fraction of circulating monocytes from patients with ECD showed signs of a constitutive activation of the MAPK pathway. Moreover, BRAF-mutated histiocytes expressed markers of OIS.

CONCLUSIONS

The oncogenic BRAF(V600E) mutation is present in biopsies and in the peripheral blood from all patients with ECD who were evaluated and is associated with OIS. These findings have significant implications for the pathogenesis, diagnosis and treatment of ECD.

摘要

目的

Erdheim-Chester 病(ECD)是一种罕见的组织细胞增生症,其特征为不受控制的慢性炎症。在最大型已发表队列中 37 例 ECD 患者的活检中,有 19 例报告存在致癌 BRAF(V600E)突变,但从未在患者的外周血中发现。此外,该突变在疾病发病机制中的作用尚未阐明。BRAF(V600E)与致癌基因诱导的衰老(OIS)有关,这是一种针对致癌事件的保护机制,其特征为诱导促炎途径。

方法

我们通过免疫组织化学和基于锁核酸 PCR 和焦磷酸测序组合的超灵敏检测法,对来自我们队列的 18 例 ECD 患者和匹配对照者的活检和外周血中的 BRAF 状态进行了验证。通过数字液滴 PCR 对发现结果进行了确认。我们还评估了 ECD 组织细胞中衰老标志物的存在。

结果

所有 ECD 患者的活检和外周血样本以及对照组均存在 BRAF(V600E)突变。ECD 组织细胞和 ECD 患者部分循环单核细胞显示 MAPK 通路持续激活的迹象。此外,BRAF 突变的组织细胞表达 OIS 的标志物。

结论

我们评估的所有 ECD 患者的活检和外周血中均存在致癌 BRAF(V600E)突变,且与 OIS 相关。这些发现对 ECD 的发病机制、诊断和治疗具有重要意义。

相似文献

1
BRAFV600E-mutation is invariably present and associated to oncogene-induced senescence in Erdheim-Chester disease.BRAFV600E 突变始终存在,并与 Erdheim-Chester 病中的癌基因诱导衰老相关。
Ann Rheum Dis. 2015 Aug;74(8):1596-602. doi: 10.1136/annrheumdis-2013-204924. Epub 2014 Mar 26.
2
Hypoalphalipoproteinemia and BRAF Mutation Are Major Predictors of Aortic Infiltration in the Erdheim-Chester Disease.低α脂蛋白血症和 BRAF 突变是 Erdheim-Chester 病主动脉浸润的主要预测因子。
Arterioscler Thromb Vasc Biol. 2018 Aug;38(8):1913-1925. doi: 10.1161/ATVBAHA.118.310803.
3
Efficacy of Combined Encorafenib and Binimetinib Treatment for Erdheim-Chester Disease Harboring Concurrent BRAF and KRAS Mutations: A Case Report.恩考芬尼与比美替尼联合治疗同时存在BRAF和KRAS突变的 Erdheim-Chester病的疗效:病例报告
Cancer Rep (Hoboken). 2024 Dec;7(12):e70093. doi: 10.1002/cnr2.70093.
4
BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease.中枢神经系统(CNS-JXG)幼年黄色肉芽肿家族性肿瘤中的 BRAF V600E 突变:包括小儿神经鞘黏液瘤病在内的修订诊断算法。
Acta Neuropathol Commun. 2019 Nov 4;7(1):168. doi: 10.1186/s40478-019-0811-6.
5
Evaluation of clinicopathologic characteristics and the BRAF V600E mutation in Erdheim-Chester disease among Chinese adults.中国成人Erdheim-Chester病的临床病理特征及BRAF V600E突变评估
Ann Hematol. 2016 Apr;95(5):745-50. doi: 10.1007/s00277-016-2606-1. Epub 2016 Feb 9.
6
Advances in Understanding and Management of Erdheim-Chester Disease.埃勒-狄克森-切斯特病的研究进展与治疗管理。
Life Sci. 2024 Jul 1;348:122692. doi: 10.1016/j.lfs.2024.122692. Epub 2024 May 6.
7
Abdominal involvement in Erdheim-Chester disease (ECD): MRI and CT imaging findings and their association with BRAF mutation. Erdheim-Chester 病(ECD)的腹部受累:MRI 和 CT 影像学表现及其与 BRAF 突变的关系。
Eur Radiol. 2018 Sep;28(9):3751-3759. doi: 10.1007/s00330-018-5326-1. Epub 2018 Mar 19.
8
BRAF V600E mutations are not an oncogenic driver of solitary xanthogranuloma and reticulohistiocytoma: Testing may be useful in screening for Erdheim-Chester disease.BRAF V600E 突变不是孤立性黄色肉芽肿和组织细胞增生症的致癌驱动因素:检测可能有助于 Erdheim-Chester 病的筛查。
Exp Mol Pathol. 2019 Dec;111:104320. doi: 10.1016/j.yexmp.2019.104320. Epub 2019 Oct 19.
9
Erdheim-Chester disease involving the breast--a rare but important differential diagnosis.累及乳腺的 Erdheim-Chester 病——一种罕见但重要的鉴别诊断。
Hum Pathol. 2015 Jan;46(1):159-64. doi: 10.1016/j.humpath.2014.10.005. Epub 2014 Oct 18.
10
Thoracic involvement in Erdheim-Chester disease: computed tomography imaging findings and their association with the BRAF mutation. Erdheim-Chester 病的胸部受累:计算机断层扫描成像表现及其与 BRAF 突变的关系。
Eur Radiol. 2018 Nov;28(11):4635-4642. doi: 10.1007/s00330-018-5421-3. Epub 2018 May 7.

引用本文的文献

1
Unraveling the molecular landscape of Erdheim-Chester disease: new insights from methylome and transcriptome integration.解析 Erdheim-Chester 病的分子图谱:甲基化组与转录组整合的新见解
Leukemia. 2025 Aug 21. doi: 10.1038/s41375-025-02742-z.
2
Recent advances in therapeutic strategies of Erdheim-Chester disease.Erdheim-Chester病治疗策略的最新进展
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jun;398(6):6407-6428. doi: 10.1007/s00210-024-03769-2. Epub 2025 Jan 21.
3
BRAF V600E mutation and high expression of PD-L1 in Rosai-Dorfman disease: case report and review of the literature.
罗萨伊-多夫曼病中BRAF V600E突变与程序性死亡配体1(PD-L1)的高表达:病例报告及文献复习
J Hematop. 2024 Dec;17(4):183-189. doi: 10.1007/s12308-024-00611-9. Epub 2024 Nov 27.
4
Erdheim-Chester disease: An elusive diagnosis in a 50-year-old Ethiopian man presenting with diffuse sclerotic bone lesion.厄尔德海姆-切斯特病:一名50岁埃塞俄比亚男性患者出现弥漫性硬化性骨病变,诊断困难。
Clin Case Rep. 2024 Sep 18;12(9):e9447. doi: 10.1002/ccr3.9447. eCollection 2024 Sep.
5
Molecular Mutations in Histiocytosis: A Comprehensive Survey of Genetic Alterations.组织细胞增多症中的分子突变:基因改变的全面综述
Mol Biotechnol. 2025 Feb;67(2):438-455. doi: 10.1007/s12033-024-01072-2. Epub 2024 Feb 20.
6
Erdheim-Chester Disease with Renal Mass Presentation: Report of the First Case From Palestine and a Review of the Literature.肾脏肿块表现的 Erdheim-Chester 病:来自巴勒斯坦的首例病例报告及文献复习。
Am J Case Rep. 2023 Nov 17;24:e941912. doi: 10.12659/AJCR.941912.
7
Erdheim-Chester Disease With BRAF V600E Mutation and Central Diabetes Insipidus Successfully Treated With Glucocorticoid.携带BRAF V600E突变及中枢性尿崩症的厄尔海姆-切斯特病经糖皮质激素治疗成功
JCEM Case Rep. 2023 Mar 17;1(2):luad014. doi: 10.1210/jcemcr/luad014. eCollection 2023 Mar.
8
Multimodality imaging of spleen involvement in Erdheim-Chester disease mimicking splenic hemangioma: a unique case report.模仿脾血管瘤的Erdheim-Chester病脾脏受累的多模态成像:一例独特病例报告
Am J Nucl Med Mol Imaging. 2023 Jun 25;13(3):118-125. eCollection 2023.
9
A case of Erdheim-Chester disease with the V600E mutation diagnosed via endoscopic sinus surgery.经内镜鼻窦手术诊断的伴有 V600E 突变的 Erdheim-Chester 病 1 例。
Nagoya J Med Sci. 2023 Feb;85(1):150-156. doi: 10.18999/nagjms.85.1.150.
10
Signaling pathways, microenvironment, and targeted treatments in Langerhans cell histiocytosis.朗格汉斯细胞组织细胞增生症中的信号通路、微环境和靶向治疗。
Cell Commun Signal. 2022 Dec 19;20(1):195. doi: 10.1186/s12964-022-00917-0.