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本文引用的文献

1
Delivery and Biosafety of Oncolytic Virotherapy.溶瘤病毒疗法的递送与生物安全性
Front Oncol. 2020 Apr 16;10:475. doi: 10.3389/fonc.2020.00475. eCollection 2020.
2
CRISPR-Cas12a: Functional overview and applications.CRISPR-Cas12a:功能概述与应用
Biomed J. 2020 Feb;43(1):8-17. doi: 10.1016/j.bj.2019.10.005. Epub 2020 Feb 5.
3
Overcoming Hurdles in Nanoparticle Clinical Translation: The Influence of Experimental Design and Surface Modification.克服纳米颗粒临床转化中的障碍:实验设计和表面修饰的影响。
Int J Mol Sci. 2019 Nov 30;20(23):6056. doi: 10.3390/ijms20236056.
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The Acidic Tumor Microenvironment as a Driver of Cancer.酸性肿瘤微环境作为癌症的驱动因素。
Annu Rev Physiol. 2020 Feb 10;82:103-126. doi: 10.1146/annurev-physiol-021119-034627. Epub 2019 Nov 15.
5
: the promising Trojan Horse in the era of precision oncology.精准肿瘤学时代有前景的特洛伊木马。
Future Oncol. 2019 Nov;15(33):3861-3876. doi: 10.2217/fon-2019-0374. Epub 2019 Oct 31.
6
De novo identification of essential protein domains from CRISPR-Cas9 tiling-sgRNA knockout screens.从头鉴定 CRISPR-Cas9 靶向 sgRNA 敲除筛选中的必需蛋白结构域。
Nat Commun. 2019 Oct 4;10(1):4541. doi: 10.1038/s41467-019-12489-8.
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Oncolytic Bacteria and their potential role in bacterium-mediated tumour therapy: a conceptual analysis.溶瘤细菌及其在细菌介导的肿瘤治疗中的潜在作用:概念分析
J Cancer. 2019 Jul 23;10(19):4442-4454. doi: 10.7150/jca.35648. eCollection 2019.
8
NSG mice as hosts for oncological precision medicine.NSG 小鼠作为肿瘤精准医学的宿主。
Lab Invest. 2020 Jan;100(1):27-37. doi: 10.1038/s41374-019-0298-6. Epub 2019 Aug 13.
9
Oncolytic bacteria: past, present and future.溶瘤细菌:过去、现在和未来。
FEMS Microbiol Lett. 2019 Jun 1;366(12). doi: 10.1093/femsle/fnz136.
10
Cancer treatment and survivorship statistics, 2019.2019 年癌症治疗与生存统计
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肿瘤治疗的下一个前沿:通过基因工程实现溶瘤细菌的临床转化。

The next frontier of oncotherapy: accomplishing clinical translation of oncolytic bacteria through genetic engineering.

机构信息

Cellular & Molecular Biology Program, North Dakota State University, Fargo, ND 58103, USA.

Pharmaceutical Sciences Department, North Dakota State University, Fargo, ND 58103, USA.

出版信息

Future Microbiol. 2021 Mar;16(5):341-368. doi: 10.2217/fmb-2020-0245. Epub 2021 Mar 23.

DOI:10.2217/fmb-2020-0245
PMID:33754804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8356681/
Abstract

The development of a 'smart' drug capable of distinguishing tumor from host cells has been sought for centuries, but the microenvironment of solid tumors continues to confound therapeutics. Solid tumors present several challenges for current oncotherapeutics, including aberrant vascularization, hypoxia, necrosis, abnormally high pH and local immune suppression. While traditional chemotherapeutics are limited by such an environment, oncolytic microbes are drawn to it - having an innate ability to selectively infect, colonize and eradicate solid tumors. Development of an oncolytic species would represent a shift in the cancer therapeutic paradigm, with ramifications reaching from the medical into the socio-economic. Modern genetic engineering techniques could be implemented to customize 'Frankenstein' bacteria with advantageous characteristics from several species.

摘要

一种能够区分肿瘤细胞和宿主细胞的“智能”药物的研发已经持续了几个世纪,但实体瘤的微环境仍然给治疗带来了困扰。实体瘤给当前的肿瘤治疗带来了一些挑战,包括血管异常、缺氧、坏死、异常高的 pH 值和局部免疫抑制。虽然传统的化疗药物受到这种环境的限制,但溶瘤微生物却被吸引到这种环境中——它们具有先天的能力,可以选择性地感染、定植和清除实体瘤。溶瘤物种的开发将代表癌症治疗范式的转变,其影响范围从医学延伸到社会经济领域。现代基因工程技术可以用来定制具有几种优势特征的“弗兰肯斯坦”细菌。