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Strong correlation between cancer progression and anti-transcription intermediary factor 1γ antibodies in dermatomyositis patients.癌症进展与皮肌炎患者抗转录中介因子 1γ 抗体之间存在强相关性。
Clin Exp Rheumatol. 2018 Nov-Dec;36(6):990-995. Epub 2018 May 8.
2
Autoantibodies in myositis.肌炎中的自身抗体。
Nat Rev Rheumatol. 2018 Apr 20;14(5):290-302. doi: 10.1038/nrrheum.2018.56.
3
Identification of multiple cancer-associated myositis-specific autoantibodies in idiopathic inflammatory myopathies: a large longitudinal cohort study.在特发性炎性肌病中鉴定多种与癌症相关的肌炎特异性自身抗体:一项大型纵向队列研究。
Arthritis Res Ther. 2017 Nov 25;19(1):259. doi: 10.1186/s13075-017-1469-8.
4
Dermatomyositis and Immune-Mediated Necrotizing Myopathies: A Window on Autoimmunity and Cancer.皮肌炎与免疫介导的坏死性肌病:自身免疫与癌症的一扇窗口
Front Immunol. 2017 Aug 21;8:992. doi: 10.3389/fimmu.2017.00992. eCollection 2017.
5
Myositis-specific autoantibodies and their association with malignancy in Italian patients with polymyositis and dermatomyositis.意大利多发性肌炎和皮肌炎患者的肌炎特异性自身抗体及其与恶性肿瘤的关联
Clin Rheumatol. 2017 Feb;36(2):469-475. doi: 10.1007/s10067-016-3453-0. Epub 2016 Oct 20.
6
Temporal relationship between cancer and myositis identifies two distinctive subgroups of cancers: impact on cancer risk and survival in patients with myositis.癌症与肌炎之间的时间关系确定了两种不同的癌症亚组:对肌炎患者癌症风险和生存的影响。
Rheumatology (Oxford). 2016 Sep;55(9):1631-41. doi: 10.1093/rheumatology/kew215. Epub 2016 May 31.
7
Idiopathic Inflammatory Myopathies and Malignancy: a Comprehensive Review.特发性炎性肌病与恶性肿瘤:全面综述。
Clin Rev Allergy Immunol. 2017 Feb;52(1):20-33. doi: 10.1007/s12016-015-8511-x.
8
Survival and cancer risk in an unselected and complete Norwegian idiopathic inflammatory myopathy cohort.一个未经选择的完整挪威特发性炎性肌病队列中的生存率和癌症风险
Semin Arthritis Rheum. 2015 Dec;45(3):301-8. doi: 10.1016/j.semarthrit.2015.06.005. Epub 2015 Jun 17.
9
Repression of TIF1γ by SOX2 promotes TGF-β-induced epithelial-mesenchymal transition in non-small-cell lung cancer.SOX2对TIF1γ的抑制促进了非小细胞肺癌中转化生长因子-β诱导的上皮-间质转化。
Oncogene. 2016 Feb 18;35(7):867-77. doi: 10.1038/onc.2015.141. Epub 2015 May 11.
10
Tumour suppressor TRIM33 targets nuclear β-catenin degradation.肿瘤抑制因子TRIM33靶向细胞核内β-连环蛋白的降解。
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中国癌症相关性肌炎患者的肌炎自身抗体分析

Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis.

作者信息

Li Liubing, Liu Chenxi, Wang Qian, Wu Chanyuan, Zhang Yanfang, Cheng Linlin, Wen Xiaoting, Zeng Xiaofeng, Zhang Fengchun, Li Yongzhe

机构信息

Department of Clinical Laboratory, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

J Clin Lab Anal. 2020 Aug;34(8):e23307. doi: 10.1002/jcla.23307. Epub 2020 Mar 27.

DOI:10.1002/jcla.23307
PMID:32222002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7439325/
Abstract

BACKGROUND

Cancer-associated myositis (CAM) has poor prognosis and causes higher mortality. In general, myositis-specific autoantibodies (MSAs) and myositis-associated autoantibodies (MAAs) have been shown to be useful biomarkers for its diagnosis.

METHODS

In the present study, focus was given in assessing the presence, prevalence, and diagnostic values of myositis autoantibodies in Chinese patients diagnosed with CAM. The sera collected from 49 CAM patients, 108 dermatomyositis/polymyositis (DM/PM) patients without cancer, 105 disease controls, and 60 healthy controls were detected for the presence of 16 autoantigens (Jo-1, OJ, EJ, PL-7, PL-12, MDA5, TIF1γ, Mi-2α, Mi-2β, SAE1, NXP2, SRP, Ku, PM-Scl75, PM-Scl100, and Ro-52) using a commercial Euroline assay.

RESULTS

The frequency of anti-TIF1γ was significantly higher in CAM patients than in DM/PM patients without cancer (46.9% vs 14.8%, P < .001). Importantly, the sensitivity and specificity for this MSA were 46.9% and 85.2%, respectively. These helped to differentiate CAM patients from DM/PM patients without cancer. However, there was no difference in other MSAs and MAAs between CAM and DM/PM patients without cancer.

CONCLUSION

The present study indicates that anti-TIF1γ levels can serve as important biomarkers for CAM diagnosis and help in distinguishing between CAM and DM/PM patients without cancer.

摘要

背景

癌症相关性肌炎(CAM)预后较差,死亡率较高。一般来说,肌炎特异性自身抗体(MSA)和肌炎相关性自身抗体(MAA)已被证明是其诊断的有用生物标志物。

方法

在本研究中,重点评估了在中国诊断为CAM的患者中肌炎自身抗体的存在、患病率和诊断价值。使用商业化的Euroline检测法,检测了从49例CAM患者、108例无癌症的皮肌炎/多发性肌炎(DM/PM)患者、105例疾病对照和60例健康对照中收集的血清中16种自身抗原(Jo-1、OJ、EJ、PL-7、PL-12、MDA5、TIF1γ、Mi-2α、Mi-2β、SAE1、NXP2、SRP、Ku、PM-Scl75、PM-Scl100和Ro-52)的存在情况。

结果

CAM患者中抗TIF1γ的频率显著高于无癌症的DM/PM患者(46.9%对14.8%,P <.001)。重要的是,这种MSA的敏感性和特异性分别为46.9%和85.2%。这些有助于将CAM患者与无癌症的DM/PM患者区分开来。然而,CAM患者与无癌症的DM/PM患者在其他MSA和MAA方面没有差异。

结论

本研究表明,抗TIF1γ水平可作为CAM诊断的重要生物标志物,并有助于区分CAM患者与无癌症的DM/PM患者。