Knapp Christopher M, He Jia, Lister John, Whitehead Kathryn A
Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Exp Biol Med (Maywood). 2016 May;241(9):1007-13. doi: 10.1177/1535370216640944. Epub 2016 Mar 27.
Conventional chemo-immunotherapy fails to cure the majority of mantle cell lymphoma patients and causes substantial toxicity. Resistant mantle cell lymphoma cells commonly overexpress and are dependent on the anti-apoptotic protein, Mcl-1, for survival. In this study, we use potent lipidoid nanoparticles to deliver siRNA to silence Mcl-1 expression. Studies were conducted using two different mantle cell lymphoma cell lines, a normal (JeKo-1) and an aggressive (MAVER-1) line, to assess the ability of lipidoid nanoparticles to be used broadly in the treatment of mantle cell lymphoma. Mcl-1 mRNA silencing and protein knockdown was observed as early as one day after treatment and the lipidoid nanoparticles achieved sustained silencing of Mcl-1 mRNA for at least four days in both JeKo-1 and MAVER-1 cells. Eighty percent silencing was achieved at three days post-transfection in JeKo-1 cells while 50% silencing was achieved in MAVER-1 cells, which are more resistant to transfection. Interestingly, silencing of Mcl-1 induced apoptosis in nearly 30% of both JeKo-1 and MAVER-1 cells three days post-transfection. Additionally, Mcl-1 silencing and the resultant apoptosis in mantle cell lymphoma cells were dose dependent. These data suggest that lipidoid nanoparticles siRNA therapy targeting Mcl-1 has potential as a new treatment modality for mantle cell lymphoma and many other cancers that overexpress Mcl-1. The combination of anti-Mcl-1 lipidoid nanoparticles with other forms of targeted therapy offers hope for reducing or replacing cytotoxic chemotherapy as standard treatment for mantle cell lymphoma.
传统的化学免疫疗法无法治愈大多数套细胞淋巴瘤患者,且会导致严重的毒性。耐药的套细胞淋巴瘤细胞通常过表达抗凋亡蛋白Mcl-1,并依赖该蛋白存活。在本研究中,我们使用强效类脂纳米颗粒递送小干扰RNA(siRNA)以沉默Mcl-1的表达。我们使用两种不同的套细胞淋巴瘤细胞系,一种是正常细胞系(JeKo-1),另一种是侵袭性细胞系(MAVER-1)进行研究,以评估类脂纳米颗粒在套细胞淋巴瘤治疗中广泛应用的能力。早在治疗一天后就观察到了Mcl-1信使核糖核酸(mRNA)沉默和蛋白敲低,并且类脂纳米颗粒在JeKo-1和MAVER-1细胞中均实现了Mcl-1 mRNA至少四天的持续沉默。在转染后三天,JeKo-1细胞实现了80%的沉默,而在对转染更具抗性的MAVER-1细胞中实现了50%的沉默。有趣的是,转染三天后,Mcl-1的沉默在JeKo-1和MAVER-1细胞中均诱导了近30%的细胞凋亡。此外,Mcl-1沉默以及套细胞淋巴瘤细胞中由此产生的凋亡具有剂量依赖性。这些数据表明,靶向Mcl-1的类脂纳米颗粒siRNA疗法有潜力成为套细胞淋巴瘤以及许多其他过表达Mcl-1的癌症的一种新治疗方式。抗Mcl-1类脂纳米颗粒与其他形式的靶向治疗相结合,为减少或替代细胞毒性化疗作为套细胞淋巴瘤的标准治疗提供了希望。