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Gut bacteria require neutrophils to promote mammary tumorigenesis
- Source :
- Oncotarget
- Publication Year :
- 2015
- Publisher :
- Impact Journals, LLC, 2015.
-
Abstract
- Recent studies suggest that gastrointestinal tract microbiota modulate cancer development in distant non-intestinal tissues. Here we tested mechanistic hypotheses using a targeted pathogenic gut microbial infection animal model with a predilection to breast cancer. FVB-Tg(C3-1-TAg)cJeg/JegJ female mice were infected by gastric gavage with Helicobacter hepaticus at three-months-of-age putting them at increased risk for mammary tumor development. Tumorigenesis was multifocal and characterized by extensive infiltrates of myeloperoxidase-positive neutrophils otherwise implicated in cancer progression in humans and animal models. To test whether neutrophils were important in etiopathogenesis in this bacteria-triggered model system, we next systemically depleted mice of neutrophils using thrice weekly intraperitoneal injections with anti-Ly-6G antibody. We found that antibody depletion entirely inhibited tumor development in this H. hepaticus-infected model. These data demonstrate that host neutrophil-associated immune responses to intestinal tract microbes significantly impact cancer progression in distal tissues such as mammary glands, and identify gut microbes as novel targets for extra-intestinal cancer therapy.
- Subjects :
- Carcinogenesis
Neutrophils
Mammary Neoplasms, Animal
Mice, Transgenic
medicine.disease_cause
Helicobacter Infections
Mice
Immune system
Breast cancer
mammary cancer
medicine
Animals
Gastrointestinal tract
Mammary tumor
Bacteria
biology
Microbiota
enteric
Cancer
medicine.disease
biology.organism_classification
3. Good health
Intestines
immune system
Oncology
Immunology
biology.protein
Female
Helicobacter hepaticus
Antibody
microbes
Research Paper
Subjects
Details
- ISSN :
- 19492553
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Oncotarget
- Accession number :
- edsair.doi.dedup.....ba83b512516b4f3a8343de6a2d362c0e
- Full Text :
- https://doi.org/10.18632/oncotarget.3328