Extratumoral Heme Oxygenase-1 (HO-1) Expressing Macrophages Likely Promote Primary and Metastatic Prostate Tumor Growth

Autor: Elin Thysell, Maria Nilsson, Sofia Halin Bergström, Anders Bergh, Anders Widmark, Emma Jernberg, Pernilla Wikström, Pär Stattin, Hanibal Hani Adamo
Jazyk: angličtina
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
Pathology
Gene Expression
lcsh:Medicine
Epithelium
White Blood Cells
Prostate cancer
0302 clinical medicine
Animal Cells
Prostate
Medicine and Health Sciences
Macrophage
Neoplasm Metastasis
lcsh:Science
Staining
Multidisciplinary
Invasive Tumors
Prostate Cancer
Prostate Diseases
Cell Staining
Neoplasm Proteins
Gene Expression Regulation
Neoplastic

medicine.anatomical_structure
Oncology
030220 oncology & carcinogenesis
Immunohistochemistry
Anatomy
Cellular Types
Research Article
PCA3
medicine.medical_specialty
Urology
Immune Cells
Immunology
Research and Analysis Methods
Gene Expression Regulation
Enzymologic

03 medical and health sciences
Exocrine Glands
Genetics
medicine
Animals
Humans
Cancer och onkologi
Blood Cells
business.industry
Macrophages
lcsh:R
Cancers and Neoplasms
Biology and Life Sciences
Prostatic Neoplasms
Cancer
Epithelial Cells
Cell Biology
medicine.disease
Rats
Heme oxygenase
Androgen receptor
Genitourinary Tract Tumors
Biological Tissue
030104 developmental biology
Metastatic Tumors
Specimen Preparation and Treatment
Cancer and Oncology
Heme Oxygenase (Decyclizing)
Prostate Gland
lcsh:Q
business
Heme Oxygenase-1
Zdroj: PLoS ONE, Vol 11, Iss 6, p e0157280 (2016)
PLoS ONE
ISSN: 1932-6203
Popis: Aggressive tumors induce tumor-supporting changes in the benign parts of the prostate. One factor that has increased expression outside prostate tumors is hemoxygenase-1 (HO-1). To investigate HO-1 expression in more detail, we analyzed samples of tumor tissue and peritumoral normal prostate tissue from rats carrying cancers with different metastatic capacity, and human prostate cancer tissue samples from primary tumors and bone metastases. In rat prostate tumor samples, immunohistochemistry and quantitative RTPCR showed that the main site of HO-1 synthesis was HO-1(+) macrophages that accumulated in the tumor-bearing organ, and at the tumor-invasive front. Small metastatic tumors were considerably more effective in attracting HO-1(+) macrophages than larger non-metastatic ones. In clinical samples, accumulation of HO-1(+) macrophages was seen at the tumor invasive front, almost exclusively in high-grade tumors, and it correlated with the presence of bone metastases. HO-1(+) macrophages, located at the tumor invasive front, were more abundant in bone metastases than in primary tumors. HO-1 expression in bone metastases was variable, and positively correlated with the expression of macrophage markers but negatively correlated with androgen receptor expression, suggesting that elevated HO-1 could be a marker for a subgroup of bone metastases. Together with another recent observation showing that selective knockout of HO-1 in macrophages reduced prostate tumor growth and metastatic capacity in animals, the results of this study suggest that extratumoral HO-1(+) macrophages may have an important role in prostate cancer.
Databáze: OpenAIRE