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Colonization of experimental murine breast tumours by Escherichia coli K-12 significantly alters the tumour microenvironment
Stephanie Weibel, 1,2,3,5 Jochen Stritzker, 2,6 Matthias Eck, 4 Werner Goebel, 1 and Aladar A. Szalay 1,2,3,5,6 *
 Departments of 1Microbiology and   2 Biochemistry, Biocenter, University of Wuerzburg, 97074 Wuerzburg, Germany.
  3 Rudolf Virchow Center, Research Center for Experimental Biomedicine, and   4 Institute of Pathology, University of Wuerzburg, 97080 Wuerzburg, Germany.
  5 Institute for Molecular Infection Biology, University of Wuerzburg, 97070 Wuerzburg, Germany.
  6 Genelux Corporation, San Diego Science Center, San Diego, CA 92109, USA.
Correspondence to   *E-mail aladar.szalay@virchow.uni-wuerzburg.de; aaszalay@genelux.com; Tel. (+49) 931 888 4410; Fax (+49) 931 888 4422.
Copyright © 2008 Blackwell Publishing Ltd

ABSTRACT

AbstractIntroductionResultsDiscussionExperimental proceduresAcknowledgementsReferences

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.


Received 16 November, 2007; accepted 3 January, 2008.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1462-5822.2008.01122.x About DOI

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