弥漫性大B细胞淋巴瘤
小RNA
癌症研究
淋巴瘤
生物
生物标志物
细胞因子信号抑制因子1
医学
免疫学
抑制器
癌症
基因
遗传学
作者
Epameinondas Koumpis,Vasileios Georgoulis,Konstantina Papathanasiou,Alexandra Papoudou‐Bai,Panagiotis Kanavaros,Evangelos Kolettas,Eleftheria Hatzimichael
出处
期刊:Biomedicines
[MDPI AG]
日期:2024-11-21
卷期号:12 (12): 2658-2658
标识
DOI:10.3390/biomedicines12122658
摘要
Diffuse Large B-cell Lymphoma (DLBCL) is the most common aggressive non-Hodgkin lymphoma (NHL). Despite the use of newer agents, such as polatuzumab vedotin, more than one-third of patients have ultimately relapsed or experienced refractory disease. MiRNAs are single-stranded, ~22-nucleotide-long RNAs that interact with their target RNA. They are significant regulators of post-transcriptional gene expression. One significant miRNA, miR-155, is involved in the pathophysiology of DLBCL and it is a critical modulator of hematopoiesis, inflammation, and immune responses. Targets of miR-155, such as histone deacetylase 4 (HDAC4), suppressor of cytokine signaling-1 (SOCS1) and immune cells, play a crucial role in DLBCL pathogenesis, since miR-155 regulates key pathways, transcription factors and cytokine expression and shapes the tumor microenvironment in DLBCL. In this review, we examine the role of miR-155 in DLBCL and its potential as a future diagnostic, prognostic, or predictive biomarker.
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