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单克隆丙种球蛋白病的衰老特征显示旁分泌衰老作为对抗疾病进展的关键防御机制。

Senescence profiling of monoclonal gammopathies reveals paracrine senescence as a crucial defense against disease progression.

作者信息

Borges Gabriel Alvares, Diaz-delCastillo Marta, Guilatco Angelo J, El-Masri Bilal Mohamad, Mustapha Fatima A, Gundesen Michael T, Hinge Maja, Lund Thomas, Abdallah Nadine, Baughn Linda B, Xu Ming, Gingery Anne, Tchkonia Tamar, Kirkland James L, Kourelis Taxiarchis, Drake Matthew T, Andersen Thomas Levin, Weivoda Megan M

机构信息

Mayo Clinic Division of Hematology, Rochester, MN, USA.

University of Aarhus, Department of Forensic Medicine, Aarhus, Denmark.

出版信息

Leukemia. 2025 May;39(5):1206-1217. doi: 10.1038/s41375-025-02572-z. Epub 2025 Mar 31.

Abstract

Multiple myeloma (MM) is a plasma cell (PC) malignancy that is preceded by monoclonal gammopathy of undetermined significance (MGUS) and/or smoldering multiple myeloma (SMM). MGUS and SMM PCs exhibit the same primary oncogenic abnormalities as MM but lack the end-organ damage that defines proliferative disease, suggesting that clonal PCs in these precursor conditions could exhibit senescence or senescence-like growth arrest. Herein we identified monoclonal gammopathy patient-derived PCs that exhibit senescence features and found that senescent PCs were significantly increased in MGUS patients compared to SMM or MM. Spatial analysis of senescent PCs in stable MGUS and SMM patient biopsies demonstrated the activation of local paracrine senescence in the bone marrow microenvironment. Stable MGUS and SMM patients also exhibited disease-specific senescence-associated secretory phenotype (SASP) signatures that significantly correlated with PC burden and clonal antibody. In contrast, progressing MGUS, SMM, and new MM patients lacked local paracrine senescence responses and robust activation of disease specific SASP signatures. Overall, these data suggest that failure to activate tumor-specific paracrine senescence responses is key to disease progression in monoclonal gammopathies.

摘要

多发性骨髓瘤(MM)是一种浆细胞(PC)恶性肿瘤,其之前存在意义未明的单克隆丙种球蛋白病(MGUS)和/或冒烟型多发性骨髓瘤(SMM)。MGUS和SMM的浆细胞表现出与MM相同的原发性致癌异常,但缺乏定义增殖性疾病的终末器官损伤,这表明这些前驱状态下的克隆性浆细胞可能表现出衰老或衰老样生长停滞。在此,我们鉴定出表现出衰老特征的单克隆丙种球蛋白病患者来源的浆细胞,并发现与SMM或MM相比,MGUS患者中衰老的浆细胞显著增加。对稳定MGUS和SMM患者活检组织中衰老浆细胞的空间分析表明,骨髓微环境中局部旁分泌衰老被激活。稳定的MGUS和SMM患者还表现出疾病特异性的衰老相关分泌表型(SASP)特征,这些特征与浆细胞负荷和克隆抗体显著相关。相比之下,进展期MGUS、SMM和新诊断的MM患者缺乏局部旁分泌衰老反应和疾病特异性SASP特征的强烈激活。总体而言,这些数据表明,未能激活肿瘤特异性旁分泌衰老反应是单克隆丙种球蛋白病疾病进展的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e688/12055601/6e453f914560/41375_2025_2572_Fig1_HTML.jpg

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