Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
PLoS One. 2010 Jul 7;5(7):e11466. doi: 10.1371/journal.pone.0011466.
Several unique biological features of HIV-1 Vpr make it a potentially powerful agent for anti-cancer therapy. First, Vpr inhibits cell proliferation by induction of cell cycle G2 arrest. Second, it induces apoptosis through multiple mechanisms, which could be significant as it may be able to overcome apoptotic resistance exhibited by many cancerous cells, and, finally, Vpr selectively kills fast growing cells in a p53-independent manner. To demonstrate the potential utility of Vpr as an anti-cancer agent, we carried out proof-of-concept studies in vitro and in vivo. Results of our preliminary studies demonstrated that Vpr induces cell cycle G2 arrest and apoptosis in a variety of cancer types. Moreover, the same Vpr effects could also be detected in some cancer cells that are resistant to anti-cancer drugs such as doxorubicin (DOX). To further illustrate the potential value of Vpr in tumor growth inhibition, we adopted a DOX-resistant neuroblastoma model by injecting SK-N-SH cells into C57BL/6N and C57BL/6J-scid/scid mice. We hypothesized that Vpr is able to block cell proliferation and induce apoptosis regardless of the drug resistance status of the tumors. Indeed, production of Vpr via adenoviral delivery to neuroblastoma cells caused G2 arrest and apoptosis in both drug naïve and DOX-resistant cells. In addition, pre-infection or intratumoral injection of vpr-expressing adenoviral particles into neuroblastoma tumors in SCID mice markedly inhibited tumor growth. Therefore, Vpr could possibly be used as a supplemental viral therapeutic agent for selective inhibition of tumor growth in anti-cancer therapy especially when other therapies stop working.
HIV-1 Vpr 的一些独特的生物学特性使其成为一种很有潜力的抗癌治疗药物。首先,Vpr 通过诱导细胞周期 G2 期阻滞来抑制细胞增殖。其次,它通过多种机制诱导细胞凋亡,这可能非常重要,因为它可能能够克服许多癌细胞表现出的凋亡抵抗,最后,Vpr 以 p53 非依赖性的方式选择性杀死快速生长的细胞。为了证明 Vpr 作为抗癌剂的潜在用途,我们进行了体外和体内的概念验证研究。我们初步研究的结果表明,Vpr 诱导多种癌症类型的细胞周期 G2 期阻滞和凋亡。此外,在一些对阿霉素(DOX)等抗癌药物耐药的癌细胞中也可以检测到相同的 Vpr 作用。为了进一步说明 Vpr 在肿瘤生长抑制中的潜在价值,我们通过向 C57BL/6N 和 C57BL/6J-scid/scid 小鼠中注射 SK-N-SH 细胞来建立 DOX 耐药神经母细胞瘤模型。我们假设 Vpr 能够阻止细胞增殖并诱导凋亡,而不管肿瘤的耐药状态如何。事实上,通过腺病毒将 Vpr 递送到神经母细胞瘤细胞中,会导致未用药和 DOX 耐药细胞的 G2 期阻滞和凋亡。此外,在 SCID 小鼠的神经母细胞瘤肿瘤中预先感染或瘤内注射表达 vpr 的腺病毒颗粒,明显抑制了肿瘤生长。因此,Vpr 可作为一种补充性病毒治疗药物,用于抗癌治疗中选择性抑制肿瘤生长,特别是当其他治疗方法失效时。