Colonization of experimental murine breast tumours by Escherichia coli K-12 significantly alters the tumour microenvironment
Article first published online: 18 JAN 2008
DOI: 10.1111/j.1462-5822.2008.01122.x
© 2008 The Authors. Journal compilation © 2008 Blackwell Publishing Ltd
Additional Information
How to Cite
Weibel, S., Stritzker, J., Eck, M., Goebel, W. and Szalay, A. A. (2008), Colonization of experimental murine breast tumours by Escherichia coli K-12 significantly alters the tumour microenvironment. Cellular Microbiology, 10: 1235–1248. doi: 10.1111/j.1462-5822.2008.01122.x
Publication History
- Issue published online: 18 JAN 2008
- Article first published online: 18 JAN 2008
- Received 16 November, 2007; accepted 3 January, 2008.
Summary
The successful application of live bacteria in cancer therapy requires a more detailed understanding of bacterial interaction with the tumour microenvironment. Here, we analysed the effect of Escherichia coli K-12 colonization on the tumour microenvironment by immunohistochemistry and fluorescence microscopy in the murine 4T1 breast carcinoma model. We described the colonization of tumour-bearing mice, as well as the spatiotemporal distribution of E. coli K-12 in the 4T1 tumour tissue over a period of 14 days. The colonization resulted within 3 days in large avascular necrotic tissue, redistribution of hypoxic areas and an enhanced collagen IV deposition within the colonized tumour tissue, which changed the tumoral perfusion of systemically injected immunoglobulins. In addition, E. coli K-12 colonization led to the redistribution of tumour-associated macrophages, forming a granulation tissue around bacterial colonies, and also to an increase in TNFα and matrix metalloproteinase 9 expression. Colonization of 4T1 tumours by E. coli K-12 resulted in strong reduction of pulmonary metastatic events. These new insights will contribute to the general understanding of the tumour–microbe cross-talk and to the design of bacterial strains with enhanced anticancer efficiency.

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