Veryaskina Yuliya A, Titov Sergei E, Kovynev Igor B, Fyodorova Sofya S, Berezina Olga V, Zhurakovskij Igor P, Antonenko Oksana V, Demakov Sergei A, Demenkov Pavel S, Ruzankin Pavel S, Tarasenko Anton S, Pospelova Tatiana I, Zhimulev Igor F
Laboratory of Molecular Genetics, Department of the Structure and Function of Chromosomes, Institute of Molecular and Cellular Biology, SB RAS, Novosibirsk 630090, Russia.
Laboratory of Gene Engineering, Institute of Cytology and Genetics, SB RAS, Novosibirsk 630090, Russia.
Cancers (Basel). 2025 Apr 12;17(8):1300. doi: 10.3390/cancers17081300.
: The heterogeneity of diffuse large B-cell lymphoma (DLBCL) based on differences in both genetic and epigenetic factors contributes to the dynamics of tumor growth and efficacy of cytoreductive therapy, as well as considerably affecting disease prognosis. This study aimed to detect microRNAs (miRNAs) capable of improving prognostic accuracy in DLBCL patients. : We performed miRNA sequencing in bone marrow (BM) samples collected from DLBCL patients. Next, the expression levels of miRNAs in lymph node (LN) samples ( = 43) and BM samples ( = 70) were analyzed by real-time RT-PCR in the group of DLBCL patients. : It was found that the expression levels of miRNA-10b, -100, -125a, -125b, -126, -143, -23a and let-7a were statistically significantly reduced in the group of DLBCL patients who had a poor prognosis compared to DLBCL patients with a favorable prognosis ( < 0.05). Kaplan-Meier survival analysis demonstrated that the upregulated expression of miRNA-23a, miRNA-125a, and miRNA-100 was associated with better overall survival in DLBCL patients. A statistically significant elevation in the expression levels of miRNA-151a, miRNA-148b and miRNA-192 in the BM samples was observed for DLBCL patients both with and without BM involvement compared to BM samples from non-cancerous blood disease (NCBD) patients ( < 0.05). Statistically significant upregulation of , , , and was observed in BM samples from DLBCL patients with and without BM involvement in comparison with BM samples from NCBD patients ( < 0.05). : miRNA-23a, miRNA-125a, and miRNA-100 were shown to be potential prognostically significant biomarkers in DLBCL patients. Changes in expression levels of miRNA-151a, miRNA-148b, miRNA-192, , , , and reflect alterations in the BM without morphological or immunophenotypic signs of a DLBCL-related BM pathology.
基于基因和表观遗传因素差异的弥漫性大B细胞淋巴瘤(DLBCL)异质性,对肿瘤生长动力学和细胞减灭治疗疗效有影响,同时也对疾病预后有显著影响。本研究旨在检测能够提高DLBCL患者预后准确性的微小RNA(miRNA)。
我们对从DLBCL患者采集的骨髓(BM)样本进行了miRNA测序。接下来,在DLBCL患者组中,通过实时逆转录聚合酶链反应(RT-PCR)分析了淋巴结(LN)样本(n = 43)和BM样本(n = 70)中miRNA的表达水平。
结果发现,与预后良好的DLBCL患者相比,预后不良的DLBCL患者组中miRNA-10b、-100、-125a、-125b、-126、-143、-23a和let-7a的表达水平在统计学上显著降低(P < 0.05)。Kaplan-Meier生存分析表明,miRNA-23a、miRNA-125a和miRNA-100的表达上调与DLBCL患者更好的总生存期相关。与非癌性血液病(NCBD)患者的BM样本相比,无论有无BM受累,DLBCL患者的BM样本中miRNA-151a、miRNA-148b和miRNA-192的表达水平均有统计学意义的升高(P < 0.05)。与NCBD患者的BM样本相比,无论有无BM受累,DLBCL患者的BM样本中miR-151a、miR-148b、miR-192以及[此处原文可能有误,缺少具体基因名称]、[此处原文可能有误,缺少具体基因名称]、[此处原文可能有误,缺少具体基因名称]和[此处原文可能有误,缺少具体基因名称]的表达在统计学上均有显著上调(P < 0.05)。
miRNA-23a、miRNA-125a和miRNA-100被证明是DLBCL患者潜在的具有预后意义的生物标志物。miRNA-151a、miRNA-148b、miRNA-192以及[此处原文可能有误,缺少具体基因名称]、[此处原文可能有误,缺少具体基因名称]、[此处原文可能有误,缺少具体基因名称]和[此处原文可能有误,缺少具体基因名称]表达水平的变化反映了BM中无DLBCL相关BM病理学形态学或免疫表型迹象的改变。