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表观遗传学改变与淋巴瘤治疗进展。

Epigenetic alterations and advancement of lymphoma treatment.

机构信息

Affiliated Hospital of Weifang Medical University, School of Clinical Medicine, Weifang Medical University, Weifang, China.

Department of Hematology, Linyi People's Hospital, Shandong University, Linyi, 276000, Shandong, China.

出版信息

Ann Hematol. 2024 May;103(5):1435-1454. doi: 10.1007/s00277-023-05395-z. Epub 2023 Aug 15.

DOI:10.1007/s00277-023-05395-z
PMID:37581713
Abstract

Lymphomas, complex and heterogeneous malignant tumors, originate from the lymphopoietic system. These tumors are notorious for their high recurrence rates and resistance to treatment, which leads to poor prognoses. As ongoing research has shown, epigenetic modifications like DNA methylation, histone modifications, non-coding RNA regulation, and RNA modifications play crucial roles in lymphoma pathogenesis. Epigenetic modification-targeting drugs have exhibited therapeutic efficacy and tolerability in both monotherapy and combination lymphoma therapy. This review discusses pathogenic mechanisms and potential epigenetic therapeutic targets in common lymphomas, offering new avenues for lymphoma diagnosis and treatment. We also discuss the shortcomings of current lymphoma treatments, while suggesting potential areas for future research, in order to improve the prediction and prognosis of lymphoma.

摘要

淋巴瘤是一种复杂且异质性的恶性肿瘤,起源于淋巴造血系统。这些肿瘤以高复发率和治疗耐药性而闻名,导致预后不良。正如正在进行的研究表明,表观遗传修饰如 DNA 甲基化、组蛋白修饰、非编码 RNA 调控和 RNA 修饰在淋巴瘤发病机制中发挥着关键作用。表观遗传修饰靶向药物在单药治疗和联合淋巴瘤治疗中均显示出治疗效果和耐受性。本综述讨论了常见淋巴瘤中的发病机制和潜在的表观遗传治疗靶点,为淋巴瘤的诊断和治疗提供了新的途径。我们还讨论了当前淋巴瘤治疗的不足之处,同时提出了未来研究的潜在方向,以改善淋巴瘤的预测和预后。

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Epigenetic alterations and advancement of lymphoma treatment.表观遗传学改变与淋巴瘤治疗进展。
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Emerging Signatures of Hematological Malignancies from Gene Expression and Transcription Factor-Gene Regulations.基因表达和转录因子-基因调控揭示血液系统恶性肿瘤的新特征
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本文引用的文献

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suppresses the tumor growth of natural killer/T-cell lymphoma via the axis.通过该轴抑制自然杀伤/T细胞淋巴瘤的肿瘤生长。
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MicroRNA-383: A tumor suppressor miRNA in human cancer.微小RNA-383:人类癌症中的一种肿瘤抑制性微小RNA。
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Valemetostat: First approval as a dual inhibitor of EZH1/2 to treat adult T-cell leukemia/lymphoma.瓦利美坦(Valemetostat):首个获批的 EZH1/2 双重抑制剂,用于治疗成人 T 细胞白血病/淋巴瘤。
CLP36通过PI3K/AKT/CREB信号通路对淋巴瘤的调控。
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YTHDC1 is a therapeutic target for B-cell acute lymphoblastic leukemia by attenuating DNA damage response through the KMT2C-H3K4me1/me3 epigenetic axis.YTHDC1通过KMT2C-H3K4me1/me3表观遗传轴减弱DNA损伤反应,是B细胞急性淋巴细胞白血病的一个治疗靶点。
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The combination of maximum standardized uptake value and clinical parameters for improving the accuracy in distinguishing primary mediastinal lymphomas from thymic epithelial tumors.最大标准化摄取值与临床参数相结合以提高区分原发性纵隔淋巴瘤与胸腺上皮肿瘤的准确性。
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Blood. 2023 Mar 9;141(10):1159-1168. doi: 10.1182/blood.2022016862.
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MiRNA-363-3p/DUSP10/JNK axis mediates chemoresistance by enhancing DNA damage repair in diffuse large B-cell lymphoma.miRNA-363-3p/DUSP10/JNK 轴通过增强弥漫性大 B 细胞淋巴瘤中的 DNA 损伤修复来介导化疗耐药性。
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SETD2 Haploinsufficiency Enhances Germinal Center-Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis.SETD2 杂合性不足增强生发中心相关的 AICDA 体细胞超突变以驱动 B 细胞淋巴瘤发生。
Cancer Discov. 2022 Jul 6;12(7):1782-1803. doi: 10.1158/2159-8290.CD-21-1514.
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Therapeutic targeting miR130b counteracts diffuse large B-cell lymphoma progression via OX40/OX40L-mediated interaction with Th17 cells.靶向治疗 miR130b 通过 OX40/OX40L 介导的与 Th17 细胞的相互作用来抵抗弥漫性大 B 细胞淋巴瘤的进展。
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lncNBAT1/APOBEC3A is a mediator of HBX-induced chemoresistance in diffuse large B cell lymphoma cells.lncNBAT1/APOBEC3A是弥漫性大B细胞淋巴瘤细胞中HBX诱导的化疗耐药性的介质。
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