High monocyte count and expression of s100a9 and s100a12 in peripheral blood mononuclear cells are associated with poor outcome in patients with metastatic prostate cancerVisa övriga samt affilieringar
2021 (Engelska)Ingår i: Cancers, ISSN 2072-6694, Vol. 13, nr 10, artikel-id 2424
Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Increasing evidence indicates calcium-binding S100 protein involvement in inflammation and tumor progression. In this prospective study, we evaluated the mRNA levels of two members of this family, S100A9 and S100A12, in peripheral blood mononuclear cells (PBMCs) in a cohort of 121 prostate cancer patients using RT-PCR. Furthermore, monocyte count was determined by flow cytometry. By stratifying patients into different risk groups, according to TNM stage, Gleason score and PSA concentration at diagnosis, expression of S100A9 and S100A12 was found to be significantly higher in patients with metastases compared to patients without clinically detectable metastases. In line with this, we observed that the protein levels of S100A9 and S100A12 in plasma were higher in patients with advanced disease. Importantly, in patients with metastases at diagnosis, high monocyte count and high levels of S100A9 and S100A12 were significantly associated with short progression free survival (PFS) after androgen deprivation therapy (ADT). High monocyte count and S100A9 levels were also associated with short cancer-specific survival, with monocyte count providing independent prognostic information. These findings indicate that circulating levels of monocytes, as well as S100A9 and S100A12, could be biomarkers for metastatic prostate cancer associated with particularly poor prognosis.
Ort, förlag, år, upplaga, sidor
MDPI, 2021. Vol. 13, nr 10, artikel-id 2424
Nyckelord [en]
Metastases, Monocytes, Peripheral blood mononuclear cells, Prostate cancer, S100A12, S100A9
Nationell ämneskategori
Cancer och onkologi
Identifikatorer
URN: urn:nbn:se:umu:diva-183631DOI: 10.3390/cancers13102424ISI: 000654662200001Scopus ID: 2-s2.0-85105817619OAI: oai:DiVA.org:umu-183631DiVA, id: diva2:1557881
2021-05-272021-05-272023-09-05Bibliografiskt granskad