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蚊虫叮咬超敏反应、慢性活动性EB病毒感染及NK/T淋巴瘤/白血病的基因表达分析

Gene expression analysis of hypersensitivity to mosquito bite, chronic active EBV infection and NK/T-lymphoma/leukemia.

作者信息

Washio Kana, Oka Takashi, Abdalkader Lamia, Muraoka Michiko, Shimada Akira, Oda Megumi, Sato Hiaki, Takata Katsuyoshi, Kagami Yoshitoyo, Shimizu Norio, Kato Seiichi, Kimura Hiroshi, Nishizaki Kazunori, Yoshino Tadashi, Tsukahara Hirokazu

机构信息

a Department of Pediatrics , Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences , Okayama , Japan.

b Department of Pathology , Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences , Okayama , Japan.

出版信息

Leuk Lymphoma. 2017 Nov;58(11):2683-2694. doi: 10.1080/10428194.2017.1304762. Epub 2017 Apr 3.

Abstract

The human herpes virus, Epstein-Barr virus (EBV), is a known oncogenic virus and plays important roles in life-threatening T/NK-cell lymphoproliferative disorders (T/NK-cell LPD) such as hypersensitivity to mosquito bite (HMB), chronic active EBV infection (CAEBV), and NK/T-cell lymphoma/leukemia. During the clinical courses of HMB and CAEBV, patients frequently develop malignant lymphomas and the diseases passively progress sequentially. In the present study, gene expression of CD16CD56-, EBV HMB, CAEBV, NK-lymphoma, and NK-leukemia cell lines, which were established from patients, was analyzed using oligonucleotide microarrays and compared to that of CD56CD16 NK cells from healthy donors. Principal components analysis showed that CAEBV and NK-lymphoma cells were relatively closely located, indicating that they had similar expression profiles. Unsupervised hierarchal clustering analyses of microarray data and gene ontology analysis revealed specific gene clusters and identified several candidate genes responsible for disease that can be used to discriminate each category of NK-LPD and NK-cell lymphoma/leukemia.

摘要

人类疱疹病毒,即爱泼斯坦-巴尔病毒(EBV),是一种已知的致癌病毒,在危及生命的T/NK细胞淋巴增殖性疾病(T/NK细胞LPD)中发挥重要作用,如蚊虫叮咬过敏(HMB)、慢性活动性EBV感染(CAEBV)以及NK/T细胞淋巴瘤/白血病。在HMB和CAEBV的临床病程中,患者经常会发展为恶性淋巴瘤,且疾病会依次被动进展。在本研究中,使用寡核苷酸微阵列分析了从患者身上建立的CD16CD56 -、EBV HMB、CAEBV、NK淋巴瘤和NK白血病细胞系的基因表达,并与健康供体的CD56CD16 NK细胞进行了比较。主成分分析表明,CAEBV和NK淋巴瘤细胞相对位置较近,表明它们具有相似的表达谱。对微阵列数据进行无监督层次聚类分析和基因本体分析,揭示了特定的基因簇,并确定了几个与疾病相关的候选基因,可用于区分各类NK-LPD以及NK细胞淋巴瘤/白血病。

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