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HIV 辅助分子病毒蛋白 R(Vpr)的抗癌活性:作为 DNA 表达质粒或生物活性肽的传递。

Anti-cancer activity of the HIV accessory molecule viral protein R (Vpr): Delivery as a DNA expression plasmid or biologically active peptides.

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, United States.

出版信息

Vaccine. 2010 Feb 23;28(8):2005-10. doi: 10.1016/j.vaccine.2009.10.060.

Abstract

By virtue of its ability to induce cell cycle arrest and apoptosis, the HIV accessory protein Vpr (viral protein R) has been evaluated by us and others as an anti-proliferative/anti-cancer agent. We have demonstrated that Vpr, when delivered to established experimental B16.F10 melanoma tumors in mice as a DNA expression plasmid through in vivo electroporation, can result in complete regression of the established tumors. We have also demonstrated that Vpr peptides from the carboxy region of the protein can inhibit in vitro growth of both B16.F10 melanoma as well as human HeLa cervical carcinoma tumor cells. These findings, summarized in this report, underscore the potential of Vpr as an anti-cancer agent and warrants, we believe, further experimental as well as clinical evaluation.

摘要

由于其诱导细胞周期停滞和细胞凋亡的能力,HIV 辅助蛋白 Vpr(病毒蛋白 R)已被我们和其他人评估为一种具有抗增殖/抗癌作用的药物。我们已经证明,当 Vpr 通过体内电穿孔作为 DNA 表达质粒递送至小鼠中已建立的实验性 B16.F10 黑色素瘤肿瘤时,可导致已建立的肿瘤完全消退。我们还证明,来自该蛋白羧基端的 Vpr 肽可以抑制体外生长的 B16.F10 黑色素瘤以及人宫颈癌细胞 HeLa。本报告总结了这些发现,突出了 Vpr 作为抗癌药物的潜力,我们认为值得进一步进行实验和临床评估。

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