Akova Ölken, Elif ORCID: 0000-0002-2784-361X; Aszodi, Attila ORCID: 0000-0003-3569-6557; Taipaleenmäki, Hanna ORCID: 0000-0002-8254-9333; Saito, Hiroaki ORCID: 0000-0002-8130-0624; Schönitzer, Veronika; Chaloupka, Michael; Apfelbeck, Maria; Böcker, Wolfgang; Saller, Maximilian Michael ORCID: 0000-0001-8774-7892 (2022): SFRP2 Overexpression Induces an Osteoblast-like Phenotype in Prostate Cancer Cells. Cells, 11 (24). p. 4081. ISSN 2073-4409
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Abstract
Prostate cancer bone metastasis is still one of the most fatal cancer diagnoses for men. Survival of the circulating prostate tumor cells and their adaptation strategy to survive in the bone niche is the key point to determining metastasis in early cancer stages. The promoter of SFRP2 gene, encoding a WNT signaling modulator, is hypermethylated in many cancer types including prostate cancer. Moreover, SFRP2 can positively regulate osteogenic differentiation in vitro and in vivo. Here, we showed SFRP2 overexpression in the prostate cancer cell line PC3 induces an epithelial mesenchymal transition (EMT), increases the attachment, and modifies the transcriptome towards an osteoblast-like phenotype (osteomimicry) in a collagen 1-dependent manner. Our data reflect a novel molecular mechanism concerning how metastasizing prostate cancer cells might increase their chance to survive within bone tissue.
Dokumententyp: | Artikel (Klinikum der LMU) |
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Organisationseinheit (Fakultäten): | 07 Medizin > Klinikum der LMU München > MUM - Muskuloskelettales Universitätszentrum München |
DFG-Fachsystematik der Wissenschaftsbereiche: | Lebenswissenschaften |
Veröffentlichungsdatum: | 09. Feb 2023 11:58 |
Letzte Änderung: | 07. Dez 2023 12:17 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/492 |
DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 491502892 |