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Morphine Promotes Tumor Angiogenesis and Increases Breast Cancer Progression
- Source :
- BioMed Research International, BioMed Research International, Vol 2015 (2015)
- Publication Year :
- 2015
- Publisher :
- Hindawi Limited, 2015.
-
Abstract
- Morphine is considered a highly potent analgesic agent used to relieve suffering of patients with cancer. Severalin vitroandin vivostudies showed that morphine also modulates angiogenesis and regulates tumour cell growth. Unfortunately, the results obtained by these studies are still contradictory. In order to better dissect the role of morphine in cancer cell growth and angiogenesis we performedin vitrostudies on ER-negative human breast carcinoma cells, MDA.MB231 andin vivostudies on heterotopic mouse model of human triple negative breast cancer, TNBC. We demonstrated that morphinein vitroenhanced the proliferation and inhibited the apoptosis of MDA.MB231 cells.In vivostudies performed on xenograft mouse model of TNBC revealed that tumours of mice treated with morphine were larger than those observed in other groups. Moreover, morphine was able to enhance the neoangiogenesis. Our data showed that morphine at clinical relevant doses promotes angiogenesis and increases breast cancer progression.
- Subjects :
- Pathology
medicine.medical_specialty
Article Subject
Angiogenesis
lcsh:Medicine
Apoptosis
Triple Negative Breast Neoplasms
General Biochemistry, Genetics and Molecular Biology
Neovascularization
Mice
Breast cancer
In vivo
Cell Line, Tumor
medicine
Animals
Humans
skin and connective tissue diseases
Triple-negative breast cancer
Cell Proliferation
Morphine
Neovascularization, Pathologic
General Immunology and Microbiology
business.industry
lcsh:R
Cell Cycle
Cancer
General Medicine
medicine.disease
Xenograft Model Antitumor Assays
Cancer cell
Disease Progression
Cancer research
Female
medicine.symptom
business
Research Article
Subjects
Details
- ISSN :
- 23146141 and 23146133
- Volume :
- 2015
- Database :
- OpenAIRE
- Journal :
- BioMed Research International
- Accession number :
- edsair.doi.dedup.....e318ec217f3c3572ab45fcd0904854eb
- Full Text :
- https://doi.org/10.1155/2015/161508