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针对钙黏蛋白异常表达和线粒体转移的多发性骨髓瘤治疗策略。

Targeting CAM-DR and Mitochondrial Transfer for the Treatment of Multiple Myeloma.

机构信息

Department of Hematology/Oncology, Tokai University School of Medicine, Isehara 259-1193, Japan.

出版信息

Curr Oncol. 2022 Nov 9;29(11):8529-8539. doi: 10.3390/curroncol29110672.

Abstract

The prognosis of patients with multiple myeloma (MM) has improved dramatically with the introduction of new therapeutic drugs, but the disease eventually becomes drug-resistant, following an intractable and incurable course. A myeloma niche (MM niche) develops in the bone marrow microenvironment and plays an important role in the drug resistance mechanism of MM. In particular, adhesion between MM cells and bone marrow stromal cells mediated by adhesion molecules induces cell adhesion-mediated drug resistance (CAM-DR). Analyses of the role of mitochondria in cancer cells, including MM cells, has revealed that the mechanism leading to drug resistance involves exchange of mitochondria between cells (mitochondrial transfer) via tunneling nanotubes (TNTs) within the MM niche. Here, we describe the discovery of these drug resistance mechanisms and the identification of promising therapeutic agents primarily targeting CAM-DR, mitochondrial transfer, and TNTs.

摘要

多发性骨髓瘤(MM)患者的预后随着新型治疗药物的引入而显著改善,但该疾病最终仍会产生耐药性,导致难治和不可治愈的病程。骨髓瘤生态位(MM 生态位)在骨髓微环境中形成,并在 MM 的耐药机制中发挥重要作用。特别是,黏附分子介导的 MM 细胞与骨髓基质细胞之间的黏附会诱导细胞黏附介导的耐药性(CAM-DR)。对包括 MM 细胞在内的癌细胞中线粒体的作用的分析表明,导致耐药性的机制涉及细胞间通过 MM 生态位内的隧道纳米管(TNTs)进行线粒体交换(线粒体转移)。在这里,我们描述了这些耐药机制的发现,以及确定了主要针对 CAM-DR、线粒体转移和 TNTs 的有前途的治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb0/9689110/a88ed21e3aa4/curroncol-29-00672-g001.jpg

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