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Overexpression of adrenomedullin gene markedly inhibits proliferation of PC3 prostate cancer cells in vitro and in vivo
Authors: Abasolo, I. (Ibane)
Yang, L. (Luping)
Haleem, R. (R.)
Xiao, W. (Weihua)
Pio, R. (Rubén)
Cuttitta, F. (Frank)
Montuenga, L.M. (Luis M.)
Kozlowski, J.M. (James M.)
Calvo, A. (Alfonso)
Wang, Z. (Zhou)
Keywords: Adrenomedullin
Prostate cancer
Growth inhibition
Issue Date: 2003
Publisher: Elsevier
Publisher version:
ISSN: 1872-8057
Citation: Abasolo I, Yang L, Haleem R, Xiao W, Pio R, Cuttitta F, et al. Overexpression of adrenomedullin gene markedly inhibits proliferation of PC3 prostate cancer cells in vitro and in vivo. Mol Cell Endocrinol 2003 Jan 31;199(1-2):179-187.
The expression of the gene encoding adrenomedullin (AM), a multifunctional peptide hormone, in the prostate is localized to the epithelial cells. Prostate cancer cells are derived from prostatic epithelial cells. To elucidate the potential role of the AM gene in prostate cancer progression, we have stably-transfected the PC3 human prostate cancer cell line with an AM gene expression vector. The AM-transfected PC3 sublines were studied along with parental and empty vector transfected PC3 cells as controls. The average level of AM in the conditioned media of AM-transfected cells was 0.959+/-0.113 nM, a physiologically relevant concentration. The ectopic expression of AM gene inhibited the proliferation of PC3 cells in culture dishes. In addition, anchorage-independent growth of the transfected sublines was virtually abolished in soft agar assays. Flow cytometry studies showed that overexpression of AM gene caused a very significant G(1)/G(0) cell cycle arrest. In vivo experiments demonstrated that AM gene expression markedly inhibited the growth of xenograft tumors in nude mice. Our in vivo and in vitro studies suggest that AM could strongly suppress the malignancy of prostate cancer cells, via autocrine and/or paracrine mechanisms.
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DA - CIMA - Oncología - Biomarcadores - Artículos de Revista

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