Iwasa Masaki, Miura Yasuo, Fujishiro Aya, Fujii Sumie, Sugino Noriko, Yoshioka Satoshi, Yokota Asumi, Hishita Terutoshi, Hirai Hideyo, Andoh Akira, Ichinohe Tatsuo, Maekawa Taira
Department of Transfusion Medicine and Cell Therapy, Kyoto University Hospital, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Department of Medicine, Shiga University of Medical Science, Shiga, 520-2192, Japan.
Int J Hematol. 2017 May;105(5):587-597. doi: 10.1007/s12185-016-2169-x. Epub 2017 Jan 2.
The poor prognosis of adults with B cell precursor acute lymphoblastic leukemia (BCP-ALL) is attributed to leukemia cells that are protected by the bone marrow (BM) microenvironment. In the present study, we explored the pharmacological targeting of mesenchymal stromal/stem cells in BM (BM-MSCs) to eliminate chemoresistant BCP-ALL cells. Human BCP-ALL cells (NALM-6 cells) that adhered to human BM-MSCs (NALM-6/Ad) were highly resistant to multiple anti-cancer drugs, and exhibited pro-survival characteristics, such as an enhanced Akt/Bcl-2 pathway and increased populations in the G0 and G2/S/M cell cycle stages. Bortezomib, a proteasome inhibitor, interfered with adhesion between BM-MSCs and NALM-6 cells and up-regulated the matricellular protein SPARC (secreted protein acidic and rich in cysteine) in BM-MSCs, thereby reducing the NALM-6/Ad population. Inhibition of SPARC expression in BM-MSCs using a small interfering RNA enhanced adhesion of NALM-6 cells. Conversely, recombinant SPARC protein interfered with adhesion of NALM-6 cells. These results suggest that SPARC disrupts adhesion between BM-MSCs and NALM-6 cells. Co-treatment with bortezomib and doxorubicin prolonged the survival of BCP-ALL xenograft mice, with a significant reduction of leukemia cells in BM. Our findings demonstrate that bortezomib contributes to the elimination of BCP-ALL cells through disruption of their adhesion to BM-MSCs, and offer a novel therapeutic strategy for BCP-ALL through targeting of BM-MSCs.
B细胞前体急性淋巴细胞白血病(BCP-ALL)成人患者预后较差,这归因于受骨髓(BM)微环境保护的白血病细胞。在本研究中,我们探索了对BM中间充质基质/干细胞(BM-MSCs)进行药物靶向治疗以消除化疗耐药的BCP-ALL细胞。黏附于人类BM-MSCs的人类BCP-ALL细胞(NALM-6细胞)(NALM-6/Ad)对多种抗癌药物具有高度抗性,并表现出促生存特征,如Akt/Bcl-2信号通路增强以及G0期和G2/S/M细胞周期阶段的细胞数量增加。蛋白酶体抑制剂硼替佐米干扰了BM-MSCs与NALM-6细胞之间的黏附,并上调了BM-MSCs中基质细胞蛋白SPARC(富含半胱氨酸的酸性分泌蛋白)的表达,从而减少了NALM-6/Ad细胞数量。使用小干扰RNA抑制BM-MSCs中SPARC的表达可增强NALM-6细胞的黏附。相反,重组SPARC蛋白干扰了NALM-6细胞的黏附。这些结果表明,SPARC破坏了BM-MSCs与NALM-6细胞之间的黏附。硼替佐米与阿霉素联合治疗可延长BCP-ALL异种移植小鼠的生存期,并显著减少BM中的白血病细胞。我们的研究结果表明,硼替佐米通过破坏BCP-ALL细胞与BM-MSCs的黏附而有助于消除这些细胞,并通过靶向BM-MSCs为BCP-ALL提供了一种新的治疗策略。