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Annexin II interactions with the annexin II receptor enhance multiple myeloma cell adhesion and growth in the bone marrow microenvironment

机译:Annexin II与Annexin II受体的相互作用增强了骨髓微环境中多发性骨髓瘤细胞的粘附和生长

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摘要

Multiple myeloma (MM) is an incurable B-cell malignancy in which the marrow microenvironment plays a critical role in our inability to cure MM. Marrow stromal cells in the microenvironment support homing, lodging, and growth of MM cells through activation of multiple signaling pathways in both MM and stromal cells. Recently, we identified annexin II (AXII) as a previously unknown factor produced by stromal cells and osteoclasts (OCL) that is involved in OCL formation, HSC and prostate cancer (PCa) homing to the BM as well as mobilization of HSC and PCa cells. AXII expressed on stromal cells supports PCa cell lodgment via the AXII receptor (AXIIR) on PCa cells, but the role of AXII and AXIIR in MM is unknown. In this study, we show that MM cells express AXIIR, that stromal/osteoblast-derived AXII facilitates adhesion of MM cells to stromal cells via AXIIR, and OCL-derived AXII enhances MM cell growth. Finally, we demonstrate that AXII activates the ERK1/2 and AKT pathways in MM cells to enhance MM cell growth. These results demonstrate that AXII and AXIIR play important roles in MM and that targeting the AXII/AXIIR axis may be a novel therapeutic approach for MM.
机译:多发性骨髓瘤(MM)是一种不可治愈的B细胞恶性肿瘤,其中骨髓微环境在我们无法治愈MM中起着关键作用。微环境中的骨髓基质细胞通过激活MM和基质细胞中的多个信号通路来支持MM细胞的归巢,倒伏和生长。最近,我们发现膜联蛋白II(AXII)是基质细胞和破骨细胞(OCL)产生的先前未知的因子,参与OCL的形成,HSC和前列腺癌(PCa)归巢于BM以及HSC和PCa细胞的动员。在基质细胞上表达的AXII通过PCa细胞上的AXII受体(AXIIR)支持PCa细胞的定位,但是AXII和AXIIR在MM中的作用尚不清楚。在这项研究中,我们表明MM细胞表达AXIIR,基质/成骨细胞衍生的AXII通过AXIIR促进MM细胞与基质细胞的粘附,而OCL衍生的AXII则促进MM细胞的生长。最后,我们证明AXII激活MM细胞中的ERK1 / 2和AKT途径来增强MM细胞的生长。这些结果表明,AXII和AXIIR在MM中起重要作用,并且以AXII / AXIIR轴为靶点可能是MM的一种新型治疗方法。

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