Local bacteria affect the efficacy of chemotherapeutic drugs
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In this study, the potential effects of bacteria on the efficacy of frequently used chemotherapies was examined. Bacteria and cancer cell lines were examined in vitro and in vivo for changes in the efficacy of cancer cell killing mediated by chemotherapeutic agents. Of 30 drugs examined in vitro, the efficacy of 10 was found to be significantly inhibited by certain bacteria, while the same bacteria improved the efficacy of six others. HPLC and mass spectrometry analyses of sample drugs (gemcitabine, fludarabine, cladribine, CB1954) demonstrated modification of drug chemical structure. The chemoresistance or increased cytotoxicity observed in vitro with sample drugs (gemcitabine and CB1954) was replicated in in vivo murine subcutaneous tumour models. These findings suggest that bacterial presence in the body due to systemic or local infection may influence tumour responses or off-target toxicity during chemotherapy.
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Of a panel of 30 chemotherapeutic drugs examined in vitro against various bacteria, 10 were inhibited and six exhibited improved efficacy linked to modification of the chemical structure of the drug for gemcitabine, fludarabine, cladribine, and CB1954.
“of a panel of 30 chemotherapeutic drugs examined in vitro against various bacteria, 10 were found to be inhibited and six exhibited improved efficacy in a way that could be linked to modification of the chemical structure of the drug in the case of gemcitabine, fludarabine, cladribine, and CB1954 (Lehouritis et al., 2015).”
From Gut reactions: Breaking down xenobiotic–microbiome interactions (2019) · cites this paper as Lehouritis et al., 2015
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- Authors
- Lehouritis, P., Cummins, J., Stanton, M., Murphy, C. T., McCarthy, F. O., Reid, G., Urbaniak, C., Byrne, W. L., & Tangney, M.
- Affiliations
- University College Cork (IE)
- Western University (CA)
- Corresponding author
- Tangney, Mark
- Venue
- Scientific Reports
- Published
- 2015-09-29
- Volume
- 5
- Issue
- 1
- Pages
- 14554-14554
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC4586607
- OpenAlex
- W1945551477
- Cited by
- 313
- References
- 54
- Citations by year
- 2026: 31 · 2025: 36 · 2024: 46 · 2023: 44 · 2022: 39 · 2021: 36 · 2020: 31 · 2019: 27 · 2018: 12 · 2017: 8 · 2016: 3
- FWCI
- 6.38
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Scholarship@Western (Western University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Cancer Research and Treatments
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Bioactive Compounds and Antitumor Agents
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer therapeutics and mechanisms
- Keywords
- bacteria, chemotherapeutic drugs, drug efficacy, chemoresistance, gemcitabine, CB1954, cladribine, fludarabine, cancer cell lines, mouse tumor model, off-target toxicity, infection and cancer
- MeSH terms
- Gemcitabine, Animals, Antineoplastic Agents, Aziridines, Biotransformation, Colonic Neoplasms, Deoxycytidine, Escherichia coli, Female, Injections, Subcutaneous, Listeria, Neoplasm Transplantation, Skin, Vidarabine, Injections, Intralesional, Treatment Outcome, Cladribine, Mice
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