d-glucuronyl C5-epimerase cell type specifically affects angiogenesis pathway in different prostate cancer cells

• Published in: Tumor biology 2014-04, Vol.35 (4), p.3237-3245
• Main Authors: Rosenberg, Eugenia E., Prudnikova, Tatiana Y., Zabarovsky, Eugene R., Kashuba, Vladimir I., Grigorieva, Elvira V.
• Format: Article
• Language: English
• Subjects: Angiogenesis; Biomarkers; Biomedical and Life Sciences; Biomedicine; Cancer Research; Carbohydrate Epimerases - physiology; Cell Line, Tumor; Gene expression; Gene Expression Profiling; Humans; Male; Medicin och hälsovetenskap; Neovascularization, Pathologic - etiology; NF-kappa B - physiology; Prostate cancer; Prostatic Neoplasms - blood supply; Prostatic Neoplasms - enzymology; Prostatic Neoplasms - genetics; Prostatic Neoplasms - pathology; Research Article
• ISSN: 1010-4283; 1423-0380; 1423-0380
• DOI: 10.1007/s13277-013-1423-6

d -glucuronyl C5-epimerase (GLCE) is involved in breast and lung carcinogenesis as a potential tumor suppressor gene, acting through inhibition of tumor angiogenesis and invasion/metastasis pathways. However, in prostate tumors, increased GLCE expression is associated with advanced disease, suggesting versatile effects of GLCE in different cancers. To investigate further the potential cancer-promoting effect of GLCE in prostate cancer, GLCE was ectopically re-expressed in morphologically different LNCaP and PC3 prostate cancer cells. Transcriptional profiles of normal PNT2 prostate cells, LNCaP, PC3 and DU145 prostate cancer cells, and GLCE-expressing LNCaP and PC3 cells were determined. Comparative analysis revealed the genes whose expression was changed in prostate cancer cells compared with normal PNT2 cells, and those differently expressed between the cancer cell lines (ACTA2, IL6, SERPINE1, TAGLN, SEMA3A, and CDH2). GLCE re-expression influenced mainly angiogenesis-involved genes (ANGPT1, SERPINE1, IGF1, PDGFB, TNF, IL8, TEK, IFNA1, and IFNB1) but in a cell type-specific manner (from basic deregulation of angiogenesis in LNCaP cells to significant activation in PC3 cells). Invasion/metastasis pathway was also affected (MMP1, MMP2, MMP9, S100A4, ITGA1, ITGB3, ERBB2, and FAS). The obtained results suggest activation of angiogenesis as a main molecular mechanism of pro-oncogenic effect of GLCE in prostate cancer. GLCE up-regulation plus expression pattern of a panel of six genes, discriminating morphologically different prostate cancer cell sub-types, is suggested as a potential marker of aggressive prostate cancer.