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间充质干细胞表达模式是多发性骨髓瘤预后的独立标志物。

The Pattern of Mesenchymal Stem Cell Expression Is an Independent Marker of Outcome in Multiple Myeloma.

机构信息

Myeloma Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

Cancer Research and Biostatistics, Seattle, Washington.

出版信息

Clin Cancer Res. 2018 Jun 15;24(12):2913-2919. doi: 10.1158/1078-0432.CCR-17-2627. Epub 2018 Mar 21.

Abstract

Mesenchymal stem cells (MSC) are an essential component of the bone marrow microenvironment and have shown to support cancer evolution in multiple myeloma. Despite the increasing evidence that multiple myeloma MSCs differ from their healthy counterparts, little knowledge exists as to whether MSCs independently influence disease outcome. The aim of this study was to determine the importance of MSCs in disease progression and outcome in multiple myeloma. To determine the impact of MSCs on multiple myeloma outcome in an system, we first identified genes from cultured MSCs that were specific to MSC expression and were not or minimally expressed in plasma cells (PC) or other cells present in bone marrow aspirates. We then applied this MSC gene signature to whole bone marrow biopsies of multiple myeloma patients compared with healthy controls and determined MSC expression scores specific to multiple myeloma and predictive of outcome. We show that multiple myeloma MSC gene expression signatures can differentiate multiple myeloma from monoclonal gammopathy and smoldering multiple myeloma (SMM) as well as from healthy controls and treated multiple myeloma patients who have achieved a complete remission. We identified a prognostic gene score based on three MSC specific genes, and , that was able to predict progression-free survival in multiple myeloma patients and progression into multiple myeloma from SMM. Our findings show that progression of multiple myeloma and of SMM into multiple myeloma does not rely solely on intrinsic PC factors, but is independently affected by the biology of the surrounding microenvironment. .

摘要

间充质干细胞(MSC)是骨髓微环境的重要组成部分,已被证明可支持多发性骨髓瘤中的肿瘤演进。尽管越来越多的证据表明多发性骨髓瘤 MSC 与其健康对应物不同,但对于 MSC 是否独立影响疾病结局,人们知之甚少。本研究旨在确定 MSC 在多发性骨髓瘤中的疾病进展和结局中的重要性。为了确定 MSC 在多发性骨髓瘤 系统中的疾病进展和结局中的重要性,我们首先鉴定了培养的 MSC 中的基因,这些基因是 MSC 表达特有的,而在浆细胞(PC)或骨髓抽吸物中存在的其他细胞中不表达或很少表达。然后,我们将这种 MSC 基因特征应用于多发性骨髓瘤患者的全骨髓活检与健康对照者进行比较,并确定与多发性骨髓瘤特异性相关且预测结局的 MSC 表达评分。我们表明,多发性骨髓瘤 MSC 基因表达特征可将多发性骨髓瘤与单克隆丙种球蛋白病和冒烟型多发性骨髓瘤(SMM)以及健康对照者和已达到完全缓解的治疗多发性骨髓瘤患者区分开来。我们基于三个 MSC 特异性基因 、 和 确定了一个预后基因评分,该评分能够预测多发性骨髓瘤患者的无进展生存期和 SMM 进展为多发性骨髓瘤。我们的研究结果表明,多发性骨髓瘤和 SMM 进展为多发性骨髓瘤不仅仅依赖于内在的 PC 因素,而是独立于周围微环境的生物学特性而受到影响。

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