Ding Yurun, Shen Yi
Department of Orthopaedic, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University 1630 Dong Fang Road, Shanghai 200127, China.
Biochem Biophys Res Commun. 2015 Nov 27;467(4):717-22. doi: 10.1016/j.bbrc.2015.10.076. Epub 2015 Oct 19.
Notch signaling activation was found in many human cancers including multiple myeloma. It was previously reported that notch contributes to drug resistant of myeloma cells upon chemotherapy treatment, inhibition of notch by inhibitors helped to overcome drug resistance. However, the mechanism of notch developed drug resistance is remained to be fully illustrated. In the current study, we reported that Notch signaling activation up-regulated expression of integrin αvβ5 in myeloma cells companied with enhanced cells adhesion on vitronectin. Silencing Notch-1 receptor with siRNA or blocking cells with integrin αvβ5 antibody reduced myeloma cells adhesion on vitronectin, importantly, vitronectin mediated adhesion confers protection of myeloma cells from drug induced apoptosis. Thus, we revealed a novel mechanism of myeloma cells resistance to drug induced apoptosis. This study first connected Notch signaling, VTN adhesion and drug resistance together. Therefore, blocking αvβ5 receptor with antibody or knock down approach would be a novel promising strategy to treat MM.
Notch信号通路激活在包括多发性骨髓瘤在内的多种人类癌症中均有发现。此前有报道称,Notch在化疗治疗时会导致骨髓瘤细胞产生耐药性,使用抑制剂抑制Notch有助于克服耐药性。然而,Notch产生耐药性的机制仍有待充分阐明。在本研究中,我们报道了Notch信号通路激活上调了骨髓瘤细胞中整合素αvβ5的表达,同时增强了细胞在玻连蛋白上的黏附。用小干扰RNA沉默Notch-1受体或用整合素αvβ5抗体阻断细胞可降低骨髓瘤细胞在玻连蛋白上的黏附,重要的是,玻连蛋白介导的黏附赋予了骨髓瘤细胞对药物诱导凋亡的保护作用。因此,我们揭示了骨髓瘤细胞对药物诱导凋亡产生抗性的一种新机制。本研究首次将Notch信号通路、玻连蛋白黏附与耐药性联系在一起。因此,用抗体或敲除方法阻断αvβ5受体将是一种治疗多发性骨髓瘤的新的有前景的策略。