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Published on: September 30, 2019
Bacteriophages displaying anticancer peptides in combined antibacterial and anticancer treatment
Krystyna Dąbrowska1, Zuzanna Kaźmierczak, Joanna Majewska
1Institute of Immunology & Experimental Therapy, Polish Academy of Sciences, Weigla 12, 53-114 Wrocław, Poland.
Aims:
Novel anticancer strategies have employed bacteriophages as drug carriers and display platforms for anticancer agents; however, bacteriophage-based platforms maintain their natural antibacterial activity. This study provides the assessment of combined anticancer (engineered) and antibacterial (natural) phage activity in therapies.
Materials & Methods:
An in vivo BALB/c mouse model of 4T1 tumor growth accompanied by surgical wound infection was applied. The wounds were located in the areas of tumors. Bacteriophages (T4) were modified with anticancer Tyr-Ile-Gly-Ser-Arg (YIGSR) peptides by phage display and injected intraperitoneally.
Results & Conclusion:
Tumor growth was decreased in mice treated with YIGSR-displaying phages. The acuteness of wounds, bacterial load and inflammatory markers in phages-treated mice were markedly decreased. Thus, engineered bacteriophages combine antibacterial and anticancer activity.
Insights
Engineered bacteriophages carrying anticancer peptides demonstrated reduced tumor growth and improved wound healing in mice. This dual-action therapy leverages natural antibacterial properties with targeted anticancer effects for novel treatments.
Area of Science:
- Biotechnology
- Oncology
- Microbiology
Background:
- Bacteriophages (phages) are explored as drug carriers for cancer therapy.
- Phages possess inherent antibacterial activity, posing a challenge for solely anticancer applications.
- Combining engineered anticancer functions with natural antibacterial properties is a novel therapeutic approach.
Purpose of the Study:
- To assess the combined anticancer and antibacterial activity of engineered bacteriophages.
- To evaluate the efficacy of bacteriophages displaying anticancer peptides in a tumor model with wound infection.
Main Methods:
- Utilized a BALB/c mouse model with 4T1 tumor growth and surgical wound infection.
- Modified T4 bacteriophages with Tyr-Ile-Gly-Ser-Arg (YIGSR) peptides via phage display.
- Administered YIGSR-displaying phages intraperitoneally.
Main Results:
- Significant decrease in tumor growth observed in mice treated with YIGSR-displaying phages.
- Marked reduction in wound severity, bacterial load, and inflammatory markers.
- Demonstrated synergistic therapeutic effects of engineered and natural phage activities.
Conclusions:
- Engineered bacteriophages effectively combine anticancer and antibacterial functions.
- This dual-action phage therapy shows promise for treating complex conditions involving tumors and infections.
- Further research into bacteriophage-based dual-action therapies is warranted.
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