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甲病毒及其衍生载体作为抗肿瘤药物。

Alphaviruses and their derived vectors as anti-tumor agents.

作者信息

Atkins Gregory J, Smyth James W P, Fleeton Marina N, Galbraith Sareen E, Sheahan Brian J

机构信息

Department of Microbiology, Moyne Institute, Trinity College, Dublin 2, Ireland.

出版信息

Curr Cancer Drug Targets. 2004 Nov;4(7):597-607. doi: 10.2174/1568009043332754.

Abstract

The alphaviruses Semliki Forest virus (SFV) and Sindbis virus have recently been developed as prototype anti-cancer agents. These are RNA-containing enveloped viruses that code for only 9 proteins of unique sequence. The standard recombinant SFV vector system consists of suicide particles containing recombinant RNA. In addition, alphavirus vectors capable of limited multiplication in the host are also being developed. Several strategies are being adopted to construct prototype SFV vectors for cancer treatment. These include: 1) construction of both prophylactic and therapeutic vaccines to stimulate immunity to tumor-associated antigens, 2) use of apoptosis induction to destroy tumor cells, which includes both the use of the inherent apoptosis-inducing ability of the vector and the action of pro-apoptotic genes cloned into the vector, and 3) expression of cytokines and other immunoregulatory proteins by the vector that enhance anti-tumor immune responses and/or inhibit tumor cell growth. This includes the use of cytokines such as IL-12 that target angiogenesis. Sindbis virus appears to have a natural tropism for tumor cells that may allow targeting both of the wild-type virus and the vector. This approach may also be useful for targeting metastases. For SFV, neurovirulence and/or neurotropism, as well as other tissue damage, may preclude the use of unmodified replication competent wild-type virus in tumor treatment. However, it may be possible to use such a virus in animals that have been vaccinated, using a vector-derived vaccine.

摘要

辛德毕斯病毒(Semliki Forest virus,SFV)和辛德毕斯病毒最近已被开发为原型抗癌药物。这些是含RNA的包膜病毒,仅编码9种具有独特序列的蛋白质。标准的重组SFV载体系统由含有重组RNA的自杀颗粒组成。此外,能够在宿主中有限增殖的甲病毒载体也在开发中。正在采用多种策略来构建用于癌症治疗的原型SFV载体。这些策略包括:1)构建预防性和治疗性疫苗以刺激对肿瘤相关抗原的免疫,2)利用凋亡诱导来破坏肿瘤细胞,这包括利用载体固有的凋亡诱导能力以及克隆到载体中的促凋亡基因的作用,3)通过载体表达细胞因子和其他免疫调节蛋白,增强抗肿瘤免疫反应和/或抑制肿瘤细胞生长。这包括使用靶向血管生成的细胞因子,如IL-12。辛德毕斯病毒似乎对肿瘤细胞具有天然嗜性,这可能允许对野生型病毒和载体进行靶向。这种方法也可能对靶向转移灶有用。对于SFV,神经毒性和/或神经嗜性以及其他组织损伤可能会妨碍在肿瘤治疗中使用未修饰的具有复制能力的野生型病毒。然而,使用源自载体的疫苗,有可能在已接种疫苗的动物中使用这种病毒。

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