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一种新型溶瘤单纯疱疹病毒,能够对 CD133± 肿瘤细胞进行细胞特异性转录靶向,诱导显著的肿瘤消退。

A Novel Oncolytic Herpes Capable of Cell-Specific Transcriptional Targeting of CD133± Cancer Cells Induces Significant Tumor Regression.

机构信息

Molecular Medicine Laboratory, The University of Kansas Medical School, Kansas, Missouri, USA.

Midwest Biomedical Research Foundation, Kansas City Veterans Affairs Medical Center, Kansas, Missouri, USA.

出版信息

Stem Cells. 2018 Aug;36(8):1154-1169. doi: 10.1002/stem.2835. Epub 2018 Jul 17.

Abstract

The topic of cancer stem cells (CSCs) is of significant importance due to its implications in our understanding of the tumor biology as well as the development of novel cancer therapeutics. However, the question of whether targeting CSCs can hamper the growth of tumors remains mainly unanswered due to the lack of specific agents for this purpose. To address this issue, we have developed the first mutated version of herpes simplex virus-1 that is transcriptionally targeted against CD133+ cells. CD133 has been portrayed as one of the most important markers in CSCs involved in the biology of a number of human cancers, including liver, brain, colon, skin, and pancreas. The virus developed in this work, Signal-Smart 2, showed specificity against CD133+ cells in three different models (hepatocellular carcinoma, colorectal cancer, and melanoma) resulting in a loss of viability and invasiveness of cancer cells. Additionally, the virus showed robust inhibitory activity against in vivo tumor growth in both preventive and therapeutic mouse models as well as orthotopic model highly relevant to potential clinical application of this virus. Therefore, we conclude that targeting CD133+ CSCs has the potential to be pursued as a novel strategy against cancer. Stem Cells 2018;36:1154-1169.

摘要

癌症干细胞(CSCs)的研究具有重要意义,因为它有助于我们理解肿瘤生物学,并为新型癌症治疗方法的开发提供了依据。然而,由于缺乏针对 CSCs 的特定药物,靶向 CSCs 是否能抑制肿瘤生长的问题仍未得到解答。为了解决这个问题,我们开发了第一个转录靶向 CD133+细胞的突变单纯疱疹病毒-1 版本。CD133 被认为是与多种人类癌症(包括肝癌、脑癌、结肠癌、皮肤癌和胰腺癌)的生物学有关的 CSCs 中最重要的标志物之一。本研究开发的病毒 Signal-Smart 2 在三种不同模型(肝癌、结直肠癌和黑色素瘤)中表现出对 CD133+细胞的特异性,导致癌细胞的活力和侵袭性丧失。此外,该病毒在预防和治疗性小鼠模型以及与该病毒的潜在临床应用高度相关的原位模型中均显示出对体内肿瘤生长的强大抑制活性。因此,我们得出结论,靶向 CD133+CSCs 作为一种新的癌症治疗策略具有一定的潜力。《干细胞》2018;36:1154-1169.

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