Kamory Eniko, Schmidt Thomas, Broquere Cedric, Peters Hartmut, Hocher Berthold
IFLb Laboratoriumsmedizin Berlin GmbH, Windscheidstraße 18, 10627 Berlin, Germany.
Hematology and Oncology, Stralsund, Germany.
J Hematol. 2017 Oct;6(4):105-108. doi: 10.14740/jh335w. Epub 2017 Sep 20.
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.
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。