4.6 Article

Methods and Techniques to Facilitate the Development of Clostridium novyi NT as an Effective, Therapeutic Oncolytic Bacteria

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.624618

关键词

CRISPR(clustered regularly interspaced short palindromic repeat); Cas9(CRISPR associated protein 9)-mediated genome editing; oncolytic bacteria; Clostridia; gene engineering; oncotherapeutics

资金

  1. NIH COBRE award [1P20 GM109024]
  2. NDSU Graduate School Dissertation Fellowship
  3. North Dakota State University COBRE [P20GM109024]

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The tumor microenvironment poses challenges for oncotherapeutics development, but oncolytic bacteria such as Clostridium novyi show promise in selectively targeting and lysing solid tumors, with the potential for immune reactivation. The study focuses on efficient experimental methods for utilizing C. novyi and aims to address gaps in knowledge regarding gene insertion techniques for further development of this oncolytic bacteria.
The tumor microenvironment is characterized by anomalous vascularization, hypoxia, and acidity at the core of solid tumors that culminates in concentrated necrosis and immune system dysregulation among other effects. While this environment presents several challenges for the development of oncotherapeutics that deliver their activity via the enhanced permeability and retention (EPR) effect of the leaky blood vessels around a tumor, oncolytic bacteria, or a class of bacteria with a noted capacity to lyse solid tumors, are attracted to the very environment found at the center of solid tumors that confounds other therapeutics. It is this capacity that allows for a potent, active penetration from the tumor margins into the core, and subsequent colonization to facilitate lysis and immune reactivation. Clostridium novyi in particular has recently shown great promise in preclinical and clinical trials when administered directly to the tumor. These studies indicate that C. novyi is uniquely poised to effectively accomplish the long sought after holy grail of oncotherapeutics: selective tumor localization via intravenous delivery. This study reports the development of efficient methods that facilitate experimental work and therapeutic translation of C. novyi including the ability to work with this obligate micro-anaerobe on the benchtop. Additionally, this study seeks to utilize this newfound experimental flexibility to address several gaps in the current knowledge regarding the efficacy of CRIPSR/Cas9-mediated gene insertion in this species to further develop this oncolytic bacteria and the genetic customization of bacteria in general.

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