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

期刊

FUTURE MICROBIOLOGY
卷 16, 期 5, 页码 341-368

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/fmb-2020-0245

关键词

cancer; CRISPR; Cas; genetic engineering; genetic modification; Gram-negative bacteria; Gram-positive bacteria; microbe– host interaction; microbial genome; oncolytic bacteria; oncotherapy

资金

  1. NIH COBRE award [1P20 GM109024]
  2. NDSU Graduate School Dissertation Fellowship
  3. Center for Diagnostic and Therapeutic Strategies in Pancreatic Cancer at North Dakota State University
  4. NDSU Graduate School Interdisciplinary Studies Doctoral Dissertation Award

向作者/读者索取更多资源

Traditional chemotherapeutics are limited by the dense nature of tumor tissue, altered blood vessels, diminished oxygenation, altered tissue pH and cellular metabolic inactivity, which hampers their effectiveness. However, some bacteria and viruses are naturally drawn to tumor environments and have the ability to selectively infect, colonize and eradicate solid tumors. Modern genetic engineering techniques could be used to customize bacteria with advantageous characteristics for potential cancer treatment.
Tweetable abstract Most drugs are inhibited by solid tumor environments, but some bacteria and viruses are drawn to it, with a natural ability to selectively infect. Modern genetic engineering could be used to customize bacteria with advantageous characteristics. Lay abstract Side effects of chemotherapeutics are thought to often be a reflection of our inability to target these toxic substances to only cancer cells; hence, scientists have spent centuries searching for alternative treatments that would confine their actions to tumor cells, sparing healthy tissue. Unfortunately, the dense nature of tumor tissue along with altered blood vessels, that lead to diminished tumor tissue oxygenation, altered tissue pH and cellular metabolic inactivity or even cell death have proven challenging. Importantly, these barriers have contributed to local and even sometimes systemic suppression of the patient's immune system that can allow the tumor to grow and progress unchecked. While most non-cancer cells are inhibited by the local tumor environment, certain microbes, including some bacteria and viruses, are drawn to it, possessing a natural ability to selectively infect, colonize and eradicate solid tumors. These microbes may also restore the patient's immune balance. However, use of these microbes is not without its own problems; nevertheless, modern genetic engineering techniques could be implemented to develop customized, safe, effective bacteria with advantageous characteristics. The development and clinical translation of cancer-fighting bacteria would represent a shift in cancer therapeutics and would have ramifications that reach beyond medical efficacy into the realm of socioeconomics. This review seeks to marry the current field of oncolytic bacteria with the expanding field of modern bacterial genetic engineering techniques in prospect of such a therapeutic. 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.

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