The role of stem/progenitor cells and wnt/β-catenin signaling pathway in the patients with prostate cancer

dc.contributor.authorVatansever H.S.
dc.contributor.authorGumus B.
dc.contributor.authorAydogdu O.
dc.contributor.authorSivrikoz O.N.
dc.contributor.authorTürkôz-Uluer E.
dc.contributor.authorKivanç M.
dc.contributor.authorAteşçi Y.Z.
dc.contributor.authorBugdayci H.
dc.date.accessioned2025-04-10T11:11:17Z
dc.date.available2025-04-10T11:11:17Z
dc.date.issued2014
dc.description.abstractAim: The aim of this paper was to investigate the possible effect of cancer stem cells (CSCs) and relationship with Wnt/β-catenin signaling pathway progressing of prostate cancer. Methods: Thirty men with a pathological diagnosis of benign prostate hyperplasia (BPH) (group 1, N.=10), prostate cancer with a gleason score of ≤6 (group 2, N.=10), and prostate cancer with a gleason score of >6 (group 3, N.=10) were included in the study. The patients' groups were compared in terms of immunoreactivity strength of prostatic stem/progenitor cell surface markers including CD133 and CD117. We also compared the immunoreactivity of Wnt7a, a part of Wnt signaling pathway which has a potential role in the progression of several cancers including prostate cancer. The immunoreactivity of Frizzled 6 (Fzd 6) which is the receptor of Wnt family was also evaluated in all groups. Results: Immunohistochemical analyses demonstrated that although CD 133 immunoreactivity was positive in all groups, immunoreactivity was significantly stronger in group 3 when compared to other groups. While CD117 immunoreactivity was negative in group 1 and 2, it was positive in group 3. Wnt7a immunoreactivity was weak in all groups and Fzd 6 immunoreactivity was stronger in group 1 and 3 when compared to group 2. Conclusion: Our findings demonstrated that CSCs and Wnt signaling pathway have a potential role in the development and progression of prostate cancer.
dc.identifier.urihttp://hdl.handle.net/20.500.14701/49471
dc.publisherEdizioni Minerva Medica
dc.titleThe role of stem/progenitor cells and wnt/β-catenin signaling pathway in the patients with prostate cancer
dc.typeArticle

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