Clostridial spores to treat solid tumours - potential for a new therapeutic modality
- PMID: 20158471
- DOI: 10.2174/156652310790945548
Clostridial spores to treat solid tumours - potential for a new therapeutic modality
Abstract
In the quest to developing novel cancer therapies, oncolytic Clostridia are re-emerging as promising candidates due to their ability to specifically target and lyse tumours with great efficacy. Clostridial spores have the innate abilities that exploit the unique tumour microenvironment by directly penetrating, colonising and killing tumour cells. These unique features have prompted many studies to investigate their oncolytic potency. In addition, Clostridia possess a number of characteristics that enable them to be developed as oncolytic gene delivery vectors, such as their unlimited capacity, antibiotic sensitivity, and extracellular existence. Similarly, numerous strategies are being devised and tested to take advantage of these features with modern molecular technologies. In this review, we detail the traits that distinguish Clostridia from other agents, and describe the potential therapeutic effects that Clostridial spores demonstrate, but are not achievable with other treatment modalities. Furthermore, we will also summarize the recent advances in the use of Clostridial spores as viable therapeutic candidates, incorporating the latest progresses in genetic engineering tools, such as ClosTron. Finally, we will highlight some avenues deserving further studies in order to realise the ultimate goal of utilizing oncolytic Clostridia clinically in patients.
Similar articles
-
Bacterial targeted tumour therapy-dawn of a new era.Cancer Lett. 2008 Jan 18;259(1):16-27. doi: 10.1016/j.canlet.2007.10.034. Cancer Lett. 2008. PMID: 18063294 Review.
-
The use of clostridial spores for cancer treatment.J Appl Microbiol. 2006 Sep;101(3):571-8. doi: 10.1111/j.1365-2672.2006.02886.x. J Appl Microbiol. 2006. PMID: 16907807 Review.
-
The potential of clostridial spores as therapeutic delivery vehicles in tumour therapy.Res Microbiol. 2015 May;166(4):244-54. doi: 10.1016/j.resmic.2014.12.006. Epub 2015 Jan 7. Res Microbiol. 2015. PMID: 25576776 Review.
-
Repeated cycles of Clostridium-directed enzyme prodrug therapy result in sustained antitumour effects in vivo.Br J Cancer. 2006 Nov 6;95(9):1212-9. doi: 10.1038/sj.bjc.6603367. Epub 2006 Oct 3. Br J Cancer. 2006. PMID: 17024128 Free PMC article.
-
Chemotherapeutic tumour targeting using clostridial spores.FEMS Microbiol Rev. 1995 Oct;17(3):357-64. doi: 10.1111/j.1574-6976.1995.tb00219.x. FEMS Microbiol Rev. 1995. PMID: 7576773 Review.
Cited by
-
Bifidobacterium breve as a delivery vector of IL-24 gene therapy for head and neck squamous cell carcinoma in vivo.Gene Ther. 2017 Nov;24(11):699-705. doi: 10.1038/gt.2017.74. Epub 2017 Aug 14. Gene Ther. 2017. PMID: 28805796
-
Live-Attenuated Bacterial Vectors: Tools for Vaccine and Therapeutic Agent Delivery.Vaccines (Basel). 2015 Nov 10;3(4):940-72. doi: 10.3390/vaccines3040940. Vaccines (Basel). 2015. PMID: 26569321 Free PMC article. Review.
-
Flavin mononucleotide-based fluorescent proteins function in mammalian cells without oxygen requirement.PLoS One. 2012;7(9):e43921. doi: 10.1371/journal.pone.0043921. Epub 2012 Sep 11. PLoS One. 2012. PMID: 22984451 Free PMC article.
-
Targeting tumors with salmonella Typhimurium- potential for therapy.Oncotarget. 2010 Dec;1(8):721-728. doi: 10.18632/oncotarget.206. Oncotarget. 2010. PMID: 21321381 Free PMC article. Review.
-
Bacteria as vectors for gene therapy of cancer.Bioeng Bugs. 2010 Nov-Dec;1(6):385-94. doi: 10.4161/bbug.1.6.13146. Bioeng Bugs. 2010. PMID: 21468205 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical