Expression of CD47 and CALR in myeloproliferative neoplasms: Potential new therapeutic targets.

C. Rinaldi, K. Boasman, M. Simmonds
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引用次数: 0

Abstract

48 Background: In solid tumours, calreticulin (CALR) overexpression produces a pro-phagocytic signal and is counteracted by concomitant expression of anti- phagocytic CD47, reflecting an apoptosis vs survival mechanism. Increases of both CALR and CD47 on the cell membrane have been observed in response to chemotherapy, however their role in myeloid malignancies is poorly understood. We investigated the expression of CALR and CD47 in patients with essential thrombocythemia (ET), polycythemia vera (PV) and myelofibrosis (MF). Methods: Mononuclear cells were collected from peripheral blood of 27 MPN patients (8 PV, 16 ET, 3 MF), and from 4 controls. In total 14 patients received cyto-reductive therapies (Hydroxyurea, Anagrelide and Ruxolitinib). Cells were fractionised into 4 compartments: membrane, cytoplasm, cytosol and nucleus. Proteins were extracted using TRIzol, with CALR and CD47 protein expression analysed by western blotting. Results: Total CALR and CD47 protein expression increased in MPN samples comparing with controls (CALR- 7.9 vs 5.1; CD47- 2.7 vs 2.2 fold). CD47 showed higher expression on MPN cells membranes when compared with CALR (22% vs 13.9%). We observed a significant reduction of CALR when patients are treated with cyto-reductive agents (ET- untreated 43.3% vs treated 2%, PV- 3.6% vs 2.2%, ET- 21% vs 11%). Interestingly we have observed a significant increase in CD47 after treatment in MF and PV (CD47 in MF- untreated 11.8% vs treated 34.3%, PV-11.4% vs 35.9%), suggesting an anti-phagocytic effect induced by cytotoxic drugs. In ET however, CD47 expression is reduced after treatment (22% vs 16.6%), suggesting instead a pro-phagocytic effect. Conclusions: CD47, is overexpressed on the membrane of patients with MPN suggesting a role for CD47 as a strong anti-phagocytic signal responsible for immune survival in MPN. MPN patients decreased CALR expression during therapy, but we observed a significant difference in CD47 expression in different MPN types. Anti-CD47 antibodies could represent a new strategy to enhance the pro-phagocytic signal via increasing the CALR expression, and in combination with standard cyto-reduction therapy, might represent a new therapeutical strategy in MPN.
骨髓增生性肿瘤中CD47和CALR的表达:潜在的新治疗靶点。
背景:在实体肿瘤中,钙网蛋白(calreticulin, CALR)的过表达产生促吞噬信号,并被伴随的抗吞噬CD47的表达抵消,反映了细胞凋亡与生存的机制。在化疗反应中,细胞膜上CALR和CD47的增加已被观察到,然而它们在髓系恶性肿瘤中的作用尚不清楚。我们研究了CALR和CD47在原发性血小板增多症(ET)、真性红细胞增多症(PV)和骨髓纤维化(MF)患者中的表达。方法:采集27例MPN患者(PV 8例,ET 16例,MF 3例)外周血单个核细胞,对照组4例。共有14例患者接受了细胞减少治疗(羟基脲、阿纳格列德和鲁索替尼)。细胞分为4个区室:膜、细胞质、胞浆和细胞核。TRIzol提取蛋白,western blotting分析CALR和CD47蛋白表达。结果:与对照组相比,MPN样品中总CALR和CD47蛋白表达增加(CALR- 7.9 vs 5.1;CD47- 2.7 vs 2.2倍)。与CALR相比,CD47在MPN细胞膜上的表达更高(22%比13.9%)。我们观察到,当患者接受细胞还原剂治疗时,CALR显著降低(ET-未治疗43.3% vs治疗2%,PV- 3.6% vs 2.2%, ET- 21% vs 11%)。有趣的是,我们观察到MF和PV治疗后CD47显著增加(MF治疗组CD47增加11.8%,vs治疗组34.3%,PV治疗组CD47增加11.4%,vs治疗组35.9%),提示细胞毒性药物诱导的抗吞噬作用。然而,在ET中,CD47表达在治疗后降低(22% vs 16.6%),表明其具有促吞噬作用。结论:CD47在MPN患者的膜上过表达,提示CD47作为一种强抗吞噬信号在MPN的免疫存活中起作用。MPN患者在治疗期间CALR表达降低,但我们观察到CD47在不同MPN类型中的表达有显著差异。抗cd47抗体可能代表了一种通过增加CALR表达来增强吞噬前信号的新策略,并且与标准的细胞减少治疗相结合,可能代表了一种新的治疗MPN的策略。
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来源期刊
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审稿时长
20 weeks
期刊介绍: The Journal of Global Oncology (JGO) is an online only, open access journal focused on cancer care, research and care delivery issues unique to countries and settings with limited healthcare resources. JGO aims to provide a home for high-quality literature that fulfills a growing need for content describing the array of challenges health care professionals in resource-constrained settings face. Article types include original reports, review articles, commentaries, correspondence/replies, special articles and editorials.
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