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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.

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。

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