利用m6A调控基因配对模型增强多发性骨髓瘤的分期

IF 3.5 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Clinical and Experimental Medicine Pub Date : 2025-01-17 DOI:10.1007/s10238-024-01526-6
Yating Deng, Hongkai Zhu, Hongling Peng
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引用次数: 0

摘要

多发性骨髓瘤(MM)以骨髓克隆浆细胞增殖为特征,对预后预测具有挑战性。我们利用m6A调控基因和嵌套LASSO方法建立了基因配对预后风险模型。- 0.133的截断值将MM样本分为高风险组和低风险组。该模型在2088例新诊断的MM样本中显示出良好的预后表现,并预测了在含硼替佐米方案失败或复发的患者对联合治疗(达拉单抗、卡非佐米、来那度胺和地塞米松)的反应,AUC为0.9。它区分了阴燃型MM和MM(截止值:- 0.45)和MM与浆细胞白血病(截止值:0.0857)。单细胞分析显示复发的风险评分较高。结合MM细胞系和样本数据,我们确定了对高危MM有效的潜在药物和靶点(ADAT2和NUP153)。将m6A风险模型与国际分期系统(ISS)相结合,提高了分层的准确性。这些见解支持MM的精确处理。
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Enhancing staging in multiple myeloma using an m6A regulatory gene-pairing model.

Multiple myeloma (MM) is characterized by clonal plasma cell proliferation in the bone marrow, challenging prognosis prediction. We developed a gene-pairing prognostic risk model using m6A regulatory genes and a nested LASSO method. A cutoff of - 0.133 categorized MM samples into high-risk and low-risk groups. The model showed strong prognostic performance in 2088 newly diagnosed MM samples and predicted response to combination therapy (daratumumab, carfilzomib, lenalidomide, and dexamethasone) in patients who failed or relapsed from bortezomib-containing regimens, with an AUC of 0.9. It distinguished between smoldering MM and MM (cutoff: - 0.45) and between MM and plasma cell leukemia (cutoff: 0.0857). Single-cell analysis revealed higher risk scores at relapse. Combining MM cell lines and sample data, we identified potential drugs and targets (ADAT2 and NUP153) effective against high-risk MM. Integrating the m6A risk model with the International Staging System (ISS) enhanced stratification accuracy. These insights support precision treatment of MM.

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来源期刊
Clinical and Experimental Medicine
Clinical and Experimental Medicine 医学-医学:研究与实验
CiteScore
4.80
自引率
2.20%
发文量
159
审稿时长
2.5 months
期刊介绍: Clinical and Experimental Medicine (CEM) is a multidisciplinary journal that aims to be a forum of scientific excellence and information exchange in relation to the basic and clinical features of the following fields: hematology, onco-hematology, oncology, virology, immunology, and rheumatology. The journal publishes reviews and editorials, experimental and preclinical studies, translational research, prospectively designed clinical trials, and epidemiological studies. Papers containing new clinical or experimental data that are likely to contribute to changes in clinical practice or the way in which a disease is thought about will be given priority due to their immediate importance. Case reports will be accepted on an exceptional basis only, and their submission is discouraged. The major criteria for publication are clarity, scientific soundness, and advances in knowledge. In compliance with the overwhelmingly prevailing request by the international scientific community, and with respect for eco-compatibility issues, CEM is now published exclusively online.
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