Wang Fengming, Shen Chuyun
Department of Hematology, Shaoxing Shangyu people's Hospital, Shaoxing, People's Republic of China.
Hematology. 2025 Dec;30(1):2445403. doi: 10.1080/16078454.2024.2445403. Epub 2024 Dec 23.
Liquid-liquid phase separation (LLPS) may affect the therapeutic sensitivity of multiple myeloma (MM). This study aimed to identify LLPS-related genes with MM prognostic values and to confirm their effects on tumor progression.
Based on public transcriptomic data, this study screened LLPS- and immune-related genes for MM-derived plasma cells. Subtypes were identified using consensus clustering, followed by comparisons using -test and survival analysis. Least absolute shrinkage and selection operator was implemented to screen prognostic signatures, and Kaplan-Meier and receiver operator characteristic curves were plotted to assess their prognostic values. After transfected with sh-DDX21, CCK8, flow cytometry, and Transwells were used to observe MM cell proliferation, apoptosis, migration, and invasion.
By overlapping LLPS- and immune-related genes, 103 genes were obtained to cluster MM samples into three subtypes, which had significant differences in survival and immune landscape. Cox regression analysis screened out and that significantly overexpressed in MM to construct a prognostic model, with superior performance in predicting MM prognostic risks. Notably, subtype2 with more adverse prognosis showed significantly elevated risk scores and was more distributed in groups with high prognostic risk. experiments confirmed that cell proliferation, invasion, and migration were significantly inhibited in MM.1S cells transfected with sh-DDX21.
LLPS-related and were novel markers to predict prognostic risk of MM. Among them, was experimentally confirmed to promote MM cell proliferation, migration and invasion. These potential prognostic markers could be targeted in future personalized therapeutic strategies for MM, potentially improving patient outcomes.
液-液相分离(LLPS)可能影响多发性骨髓瘤(MM)的治疗敏感性。本研究旨在鉴定具有MM预后价值的LLPS相关基因,并证实它们对肿瘤进展的影响。
基于公开的转录组数据,本研究筛选了MM来源的浆细胞中与LLPS和免疫相关的基因。使用一致性聚类鉴定亚型,随后使用t检验和生存分析进行比较。实施最小绝对收缩和选择算子以筛选预后特征,并绘制Kaplan-Meier曲线和受试者工作特征曲线以评估其预后价值。用sh-DDX21转染后,使用CCK8、流式细胞术和Transwell实验观察MM细胞的增殖、凋亡、迁移和侵袭。
通过重叠LLPS和免疫相关基因,获得103个基因将MM样本聚类为三个亚型,它们在生存和免疫格局上有显著差异。Cox回归分析筛选出在MM中显著过表达的DDX21和RBM14以构建预后模型,在预测MM预后风险方面具有卓越性能。值得注意的是,预后较差的亚型2显示风险评分显著升高,且更多分布于高预后风险组。实验证实,用sh-DDX21转染的MM.1S细胞的增殖、侵袭和迁移受到显著抑制。
LLPS相关的DDX21和RBM14是预测MM预后风险的新标志物。其中,实验证实DDX21可促进MM细胞增殖、迁移和侵袭。这些潜在的预后标志物可作为未来MM个性化治疗策略的靶点,有望改善患者预后。