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确定经典型霍奇金淋巴瘤发病机制中功能相关的微小RNA

Pinpointing Functionally Relevant miRNAs in Classical Hodgkin Lymphoma Pathogenesis.

作者信息

Pan Yujia, Cengiz Roza, Kluiver Joost, Diepstra Arjan, Van den Berg Anke

机构信息

Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, 9713 RB Groningen, The Netherlands.

出版信息

Cancers (Basel). 2024 Mar 12;16(6):1126. doi: 10.3390/cancers16061126.

Abstract

Classical Hodgkin lymphoma (cHL) is a hematological malignancy of B-cell origin. The tumor cells in cHL are referred to as Hodgkin and Reed-Sternberg (HRS) cells. This review provides an overview of the currently known miRNA-target gene interactions. In addition, we pinpointed other potential regulatory roles of microRNAs (miRNAs) by focusing on genes related to processes relevant for cHL pathogenesis, i.e., loss of B-cell phenotypes, immune evasion, and growth support. A cHL-specific miRNA signature was generated based on the available profiling studies. The interactions relevant for cHL were extracted by comprehensively reviewing the existing studies on validated miRNA-target gene interactions. The miRNAs with potential critical roles included miR-155-5p, miR-148a-3p, miR-181a-5p, miR-200, miR-23a-3p, miR-125a/b, miR-130a-3p, miR-138, and miR-143-3p, which target, amongst others, PU.1, ETS1, HLA-I, PD-L1, and NF-κB component genes. Overall, we provide a comprehensive perspective on the relevant miRNA-target gene interactions which can also serve as a foundation for future functional studies into the specific roles of the selected miRNAs in cHL pathogenesis.

摘要

经典型霍奇金淋巴瘤(cHL)是一种起源于B细胞的血液系统恶性肿瘤。cHL中的肿瘤细胞被称为霍奇金和里德-斯腾伯格(HRS)细胞。本综述概述了目前已知的miRNA-靶基因相互作用。此外,我们通过关注与cHL发病机制相关过程的基因,即B细胞表型丧失、免疫逃逸和生长支持,确定了微小RNA(miRNA)的其他潜在调控作用。基于现有的分析研究生成了cHL特异性的miRNA特征。通过全面回顾关于已验证的miRNA-靶基因相互作用的现有研究,提取了与cHL相关的相互作用。具有潜在关键作用的miRNA包括miR-155-5p、miR-148a-3p、miR-181a-5p、miR-200、miR-23a-3p、miR-125a/b、miR-130a-3p、miR-138和miR-143-3p,它们靶向包括PU.1、ETS1、HLA-I、PD-L1和NF-κB组成基因在内的多种基因。总体而言,我们提供了关于相关miRNA-靶基因相互作用的全面观点,这也可为未来对所选miRNA在cHL发病机制中具体作用的功能研究奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1035/10968648/81743becce58/cancers-16-01126-g001.jpg

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