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Fetuin-A Promotes 3-Dimensional Growth in LNCaP Prostate Cancer Cells by Sequestering Extracellular Vesicles to Their Surfaces to Act as Signaling Platforms
Authors:Josiah Ochieng  Olga Y. Korolkova  Guoliang Li  Renjie Jin  Zhenbang Chen  Robert J. Matusik  Samuel Adunyah  Amos M. Sakwe  Olugbemiga Ogunkua
Affiliation:1.Department of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN 37208, USA; (O.Y.K.); (G.L.); (Z.C.); (S.A.); (A.M.S.); (O.O.);2.Department of Urology and Vanderbilt –Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN 37209, USA; (R.J.); (R.J.M.)
Abstract:The present studies were conducted to evaluate key serum proteins and other components that mediate anchorage-independent growth (3-D growth) of LNCaP prostate cancer cells as spheroids. The cells were cultured on ultra-low attachment plates in the absence and presence of fetuin-A and with or without extracellular vesicles. The data show that fetuin-A (alpha 2HS glycoprotein) is the serum protein that mediates 3-D growth in these cells. It does so by sequestering extracellular vesicles of various sizes on the surfaces of rounded cells that grow as spheroids. These vesicles in turn transmit growth signals such as the activation of AKT and MAP kinases in a pattern that differs from the activation of these key growth signaling pathways in adherent and spread cells growing in 2-D. In the process of orchestrating the movement and disposition of extracellular vesicles on these cells, fetuin-A is readily internalized in adhered and spread cells but remains on the surfaces of non-adherent cells. Taken together, our studies suggest the presence of distinct signaling domains or scaffolding platforms on the surfaces of prostate tumor cells growing in 3-D compared to 2-D.
Keywords:fetuin-A   vesicles   exosomes   3-dimensional   2-dimensional   growth   anchorage   signaling   prostate   cancer
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