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血管免疫母细胞性T细胞淋巴瘤中循环肿瘤DNA的检测

Detection of the circulating tumor DNAs in angioimmunoblastic T- cell lymphoma.

作者信息

Sakata-Yanagimoto Mamiko, Nakamoto-Matsubara Rie, Komori Daisuke, Nguyen Tran B, Hattori Keiichiro, Nanmoku Toru, Kato Takayasu, Kurita Naoki, Yokoyama Yasuhisa, Obara Naoshi, Hasegawa Yuichi, Shinagawa Atsushi, Chiba Shigeru

机构信息

Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.

Department of Hematology, University of Tsukuba Hospital, 2-1-1 Amakubo, Tsukuba, Ibaraki, 305-8576, Japan.

出版信息

Ann Hematol. 2017 Sep;96(9):1471-1475. doi: 10.1007/s00277-017-3038-2. Epub 2017 Jun 20.

Abstract

Recent genetic studies identified that the disease-specific G17V RHOA mutation, together with mutations in TET2, DNMT3A, and IDH2, is a hallmark of angioimmunoblastic T cell lymphomas (AITL). The diagnostic value of these mutations is now being investigated. Circulating tumor DNAs (ctDNAs) may offer a non-invasive testing for diagnosis and disease monitoring of cancers. To investigate whether these mutations are useful markers for ctDNAs in AITL and its related lymphomas, we performed targeted sequencing for TET2, RHOA, DNMT3A, and IDH2 in paired tumors and cell-free DNAs from 14 patients at diagnosis. Eighty-three percent of mutations detected in tumors were also observed in cell-free DNAs. During the disease course, mutations were detectable in cell-free DNAs in a refractory case, while they disappeared in a chemosensitive case. These data suggest that the disease-specific gene mutations serve as sensitive indicators for ctDNAs and may also be applicable for non-invasive monitoring of minimal residual diseases in AITL.

摘要

最近的基因研究发现,疾病特异性的G17V RHOA突变,连同TET2、DNMT3A和IDH2的突变,是血管免疫母细胞性T细胞淋巴瘤(AITL)的一个标志。目前正在研究这些突变的诊断价值。循环肿瘤DNA(ctDNA)可能为癌症的诊断和疾病监测提供一种非侵入性检测方法。为了研究这些突变是否是AITL及其相关淋巴瘤中ctDNA的有用标志物,我们对14例诊断时的配对肿瘤和游离DNA中的TET2、RHOA、DNMT3A和IDH2进行了靶向测序。在肿瘤中检测到的83%的突变也在游离DNA中观察到。在疾病过程中,在一例难治性病例的游离DNA中可检测到突变,而在一例化疗敏感病例中突变消失。这些数据表明,疾病特异性基因突变是ctDNA的敏感指标,也可能适用于AITL微小残留病的非侵入性监测。

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