Premium
Effects of adipocytes on the proliferation and differentiation of prostate cancer cells in a 3‐D culture model
Author(s) -
Kaneko Arata,
Satoh Yuji,
Tokuda Yuji,
Fujiyama Chisato,
Udo Kazuma,
Uozumi Jiro
Publication year - 2010
Publication title -
international journal of urology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.172
H-Index - 67
eISSN - 1442-2042
pISSN - 0919-8172
DOI - 10.1111/j.1442-2042.2010.02472.x
Subject(s) - du145 , lncap , prostate cancer , pi3k/akt/mtor pathway , protein kinase b , cell growth , cancer research , tensin , endocrinology , medicine , cancer cell , pten , cell culture , cancer , microbiology and biotechnology , biology , phosphorylation , signal transduction , biochemistry , genetics
Objective: To investigate how the mechanism of adipocyte–prostate cancer cell interaction affects the proliferation and differentiation of prostate cancer cells. Methods: An androgen‐dependent cell line (LNCaP), two androgen‐independent cell lines (PC‐3, DU145), and mature adipocytes harvested from male Wistar rats were used. Cancer cells were co‐cultured with the isolated mature adipocytes in 3‐D collagen gel matrix culture. The morphology and proliferative ability of the prostate cancer cells were examined. With regard to the activation of the phosphatidylinositol 3‐kinase (PI3K) pathway, the expression of phosphatase and tensin homologue deleted on chromosome ten (PTEN), Akt and Bad were determined by immunohistochemistry. Results: LNCaP cells co‐cultured with adipocytes formed larger clusters than those of the control. PC‐3 cells co‐cultured with adipocytes did not form larger clusters, but formed spherical and spindle‐shaped cells. The phosphorylation of Akt in PC‐3 cells was greater in the co‐cultured group compared with the controls, but there were no significant differences in the phosphorylation of Akt with regard to LNCaP and DU145 cells. Conclusions: Adipocytes could modulate the proliferation and differentiation of prostate cancer cell lines. Activation of the PI3K pathway might be involved in the prostate cancer cell–adipocyte interaction.