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一名原发性血小板增多症患者的两种新型单等位基因钙网蛋白突变

Two Novel Monoallelic Calreticulin Mutations in a Patient With Essential Thrombocythemia.

作者信息

Kamory Eniko, Schmidt Thomas, Broquere Cedric, Peters Hartmut, Hocher Berthold

机构信息

IFLb Laboratoriumsmedizin Berlin GmbH, Windscheidstraße 18, 10627 Berlin, Germany.

Hematology and Oncology, Stralsund, Germany.

出版信息

J Hematol. 2017 Oct;6(4):105-108. doi: 10.14740/jh335w. Epub 2017 Sep 20.

Abstract

Recently, mutations have been identified in the calreticulin (CALR) gene in JAK2 or myeloproliferative leukemia negative patients with myeloproliferative neoplasm. A 49-year-old male patient with incidental thrombocytosis was investigated for CALR mutation by direct sequencing method. The patient carried two novel monoallelic somatic mutations, the L367fs*52 and the p.R368W in the CALR gen, which resulted in a novel C-terminal sequence. The absent endoplasmatic reticulum retention signal in the mutant CALR results in an altered subcellular localization of the mutant protein. The new positively charged C-terminal domain has an importance for oncogenicity, effecting different signaling pathways, activating the cytokine-independent growth of the cells and down-regulating the apoptotic signaling. But the new, alternative C-terminal domain offers an opportunity for immunologic therapy as it represents a cancer-specific epitope.

摘要

最近,在患有骨髓增殖性肿瘤的JAK2或骨髓增殖性白血病阴性患者的钙网蛋白(CALR)基因中发现了突变。一名49岁偶然发现血小板增多的男性患者通过直接测序法对CALR突变进行了研究。该患者携带两个新的单等位基因体细胞突变,即CALR基因中的L367fs*52和p.R368W,这导致了一个新的C末端序列。突变型CALR中内质网保留信号的缺失导致突变蛋白的亚细胞定位改变。新的带正电荷的C末端结构域对致癌性很重要,影响不同的信号通路,激活细胞的细胞因子非依赖性生长并下调凋亡信号。但新的、替代的C末端结构域提供了免疫治疗的机会,因为它代表了一个癌症特异性表位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556c/7155843/8220da2c7b94/jh-06-105-g001.jpg

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