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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.

DOI:10.14740/jh335w
PMID:32300403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7155843/
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/7155843/10031cf03120/jh-06-105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556c/7155843/8220da2c7b94/jh-06-105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556c/7155843/10031cf03120/jh-06-105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556c/7155843/8220da2c7b94/jh-06-105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556c/7155843/10031cf03120/jh-06-105-g002.jpg

相似文献

1
Two Novel Monoallelic Calreticulin Mutations in a Patient With Essential Thrombocythemia.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
J Hematol. 2017 Oct;6(4):105-108. doi: 10.14740/jh335w. Epub 2017 Sep 20.
2
Somatic mutations of calreticulin in myeloproliferative neoplasms.髓系增殖性肿瘤中的钙网织蛋白体细胞突变。
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[Mutation of CALR Gene in Patients with Chronic Myeloproliferative Neoplasm and Its Clinical Significance].慢性髓性增殖性肿瘤患者CALR基因的突变及其临床意义
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Mutation specific immunohistochemistry is highly specific for the presence of calreticulin mutations in myeloproliferative neoplasms.突变特异性免疫组化对骨髓增殖性肿瘤中钙网蛋白突变的存在具有高度特异性。
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Calreticulin mutation does not contribute to disease progression in essential thrombocythemia by inhibiting phagocytosis.钙网蛋白突变不会通过抑制吞噬作用促进原发性血小板增多症的疾病进展。
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Calreticulin mutation specific CAL2 immunohistochemistry accurately identifies rare calreticulin mutations in myeloproliferative neoplasms.钙网织蛋白突变特异性 CAL2 免疫组化可准确识别骨髓增殖性肿瘤中的罕见钙网织蛋白突变。
Pathology. 2019 Apr;51(3):301-307. doi: 10.1016/j.pathol.2018.11.007. Epub 2018 Dec 31.

本文引用的文献

1
Guidelines for the management of myeloproliferative neoplasms.骨髓增殖性肿瘤管理指南
Korean J Intern Med. 2015 Nov;30(6):771-88. doi: 10.3904/kjim.2015.30.6.771. Epub 2015 Oct 30.
2
CALR, JAK2, and MPL mutation profiles in patients with four different subtypes of myeloproliferative neoplasms: primary myelofibrosis, essential thrombocythemia, polycythemia vera, and myeloproliferative neoplasm, unclassifiable.四种不同亚型骨髓增殖性肿瘤患者(原发性骨髓纤维化、原发性血小板增多症、真性红细胞增多症和无法分类的骨髓增殖性肿瘤)的CALR、JAK2和MPL突变谱
Am J Clin Pathol. 2015 May;143(5):635-44. doi: 10.1309/AJCPUAAC16LIWZMM.
3
Calreticulin gene mutations in myeloproliferative neoplasms without Janus kinase 2 mutations.
无Janus激酶2突变的骨髓增殖性肿瘤中的钙网蛋白基因突变
Leuk Lymphoma. 2015 Jun;56(6):1593-8. doi: 10.3109/10428194.2014.953153. Epub 2014 Oct 7.
4
Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: a collaborative study of 1027 patients.1 型与 2 型钙网织蛋白突变在原发性血小板增多症中的比较:一项 1027 例患者的协作研究。
Am J Hematol. 2014 Aug;89(8):E121-4. doi: 10.1002/ajh.23743. Epub 2014 May 16.
5
Type 1 vs type 2 calreticulin mutations in primary myelofibrosis: differences in phenotype and prognostic impact.原发性骨髓纤维化中1型与2型钙网蛋白突变:表型差异及预后影响
Leukemia. 2014 Jul;28(7):1568-70. doi: 10.1038/leu.2014.83. Epub 2014 Feb 26.
6
The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients.原发性骨髓纤维化中预后不良突变的数量和预后:一项对 797 例患者的国际研究。
Leukemia. 2014 Sep;28(9):1804-10. doi: 10.1038/leu.2014.76. Epub 2014 Feb 19.
7
CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons.CALR 突变与 JAK2 突变、MPL 突变或三阴性骨髓纤维化的临床、细胞遗传学和分子比较。
Leukemia. 2014 Jul;28(7):1472-7. doi: 10.1038/leu.2014.3. Epub 2014 Jan 9.
8
Impact of calreticulin mutations on clinical and hematological phenotype and outcome in essential thrombocythemia.钙网织蛋白突变对原发性血小板增多症的临床和血液学表型及预后的影响。
Blood. 2014 Mar 6;123(10):1552-5. doi: 10.1182/blood-2013-11-538983. Epub 2013 Dec 26.
9
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2.伴有未突变 JAK2 的骨髓增殖性肿瘤中的体细胞 CALR 突变。
N Engl J Med. 2013 Dec 19;369(25):2391-2405. doi: 10.1056/NEJMoa1312542. Epub 2013 Dec 10.
10
Somatic mutations of calreticulin in myeloproliferative neoplasms.髓系增殖性肿瘤中的钙网织蛋白体细胞突变。
N Engl J Med. 2013 Dec 19;369(25):2379-90. doi: 10.1056/NEJMoa1311347. Epub 2013 Dec 10.