新城疫病毒、利妥昔单抗和多柔比星联合疗法作为抗血液恶性肿瘤疗法。

IF 6.7
Oncolytic Virotherapy Pub Date : 2016-04-20 eCollection Date: 2016-01-01 DOI:10.2147/OV.S95250
Ahmed Majeed Al-Shammari, Huda Rameez, Maha F Al-Taee
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引用次数: 0

摘要

血液恶性肿瘤是需要更强大疗法的重要疾病。即使是目前的靶向疗法,如利妥昔单抗和其他化疗药物,也需要开发新的治疗策略。联合疗法似乎是通过不同机制靶向肿瘤细胞的最佳选择。病毒疗法是一种非常有前途的治疗方式,因为它具有选择性、安全性,并能对癌症造成破坏。伊拉克新城疫病毒(NDV)毒株已被证明在体外和体内均有效。在目前的工作中,我们测试了其抗血液肿瘤的能力,并通过联合疗法增强了目前的治疗效果,还利用 Chou-Talalay 分析法研究了这种联合疗法。结果表明,NDV 与多柔比星在低剂量时对浆细胞瘤细胞有协同作用,p53 通路不参与其中,但当这种联合疗法用于非霍奇金淋巴瘤细胞时,p53 通路参与其中。NDV 与利妥昔单抗联用可增强细胞毒性,但与 p53 无关。总之,这项研究提出了一种治疗某些血液恶性肿瘤的新型联合疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy.

Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy.

Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy.

Newcastle disease virus, rituximab, and doxorubicin combination as anti-hematological malignancy therapy.

Hematological malignancies are important diseases that need more powerful therapeutics. Even with current targeting therapies, such as rituximab and other chemotherapeutic agents, there is a need to develop new treatment strategies. Combination therapy seems the best option to target the tumor cells by different mechanisms. Virotherapy is a very promising treatment modality, as it is selective, safe, and causes cancer destruction. The Iraqi strain of Newcastle disease virus (NDV) has proved to be effective both in vitro and in vivo. In the current work, we tested its ability on anti-hematological tumors and enhanced current treatments with combination therapy, and studied this combination using Chou-Talalay analysis. p53 concentration was measured to evaluate the mechanism of this proposed synergism. The results showed that NDV was synergistic with doxorubicin in low doses on plasmacytoma cells, with no involvement of p53 pathways, but involved p53 when the combination was used on non-Hodgkin lymphoma cells. NDV in combination with rituximab showed enhanced cytotoxicity that was p53-independent. In conclusion, this work proposes a novel combination modality for treatment of some hematological malignancies.

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