A-to-I RNA编辑在血液免疫和恶性肿瘤中的作用。

IF 2.1 4区 医学 Q2 HEMATOLOGY
Wei Liang Gan , Leilei Chen
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引用次数: 0

摘要

血细胞表现出与RNA编辑的深刻关系,特别是腺苷脱氨酶作用于RNA 1 (ADAR1)依赖的腺苷到肌苷(a -to- i) RNA编辑,影响免疫细胞活性,血液恶性肿瘤,并最终决定治疗方案的疗效,如免疫检查点抑制剂(ICIs)。这篇综述强调了A-to-I RNA编辑在白细胞中发挥的无数作用,特别关注其对免疫细胞发育和成熟的调节,以及其失调如何导致恶性造血。随着ICIs作为癌症治疗手段的越来越多的实施,有必要评估我们对免疫细胞中A-to-I RNA编辑的理解,以改善癌症治疗方式。摘要:血细胞表现出与RNA编辑的深刻关系,特别是腺苷脱氨酶作用于RNA 1 (ADAR1)依赖的腺苷到肌苷(a -to- i) RNA编辑,影响免疫细胞活性,血液恶性肿瘤,并最终决定治疗方案的疗效,如免疫检查点抑制剂(ICIs)。因此,回顾我们对免疫细胞中A-to-I RNA编辑和ADAR1的理解,以及这如何影响它们在癌症和免疫治疗中的活性是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A-to-I RNA editing in hematologic immunity and malignancy
Blood cells exhibit a profound relationship with RNA editing, particularly adenosine deaminase acting on RNA 1 (ADAR1)-dependent adenosine-to-inosine (A-to-I) RNA editing, impacting immune cell activity, hematologic malignancy, and ultimately determining the efficacy of treatment options such as immune checkpoint inhibitors (ICIs). This review highlights the myriad roles A-to-I RNA editing plays in leukocytes, with particular focus on its regulation of immune cell development and maturation, and how its dysregulation contributes to malignant hematopoiesis. With the growing implementation of ICIs as cancer therapeutics, it is imperative to take stock of our understanding of A-to-I RNA editing in immune cells to improve cancer treatment modalities.
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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
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