DU145 were plated on 96-well microplates and Pro-DeliverIN was added after mixing with protein FABP4 (0 or 100 ng) ad oleic acid (0 or 10 µg/mL) for 10 min at room temperature.
This article demonstrates the high efficiency of Pro-DeliverIN transfection reagent from OZ Biosciences to deliver proteins in human prostate cancer cell line DU 145.article reference: Int J Cancer. 2014 Apr 17. doi: 10.1002/ijc.28903.
Exogenous fatty acid binding protein 4 promotes human prostate cancer cell progression.
Abstract
Epidemiologic studies have found that
obesity is associated with malignant grade and mortality in prostate
cancer. Several adipokines have been implicated as putative mediating
factors between obesity and prostate cancer. Fatty acid binding protein 4
(FABP4), a member of the cytoplasmic fatty acid binding protein
multigene family, was recently identified as a novel adipokine. Although
FABP4 is released from adipocytes and mean circulating concentrations
of FABP4 are linked with obesity, effects of exogenous FABP4 on prostate
cancer progression are unclear. In this study, we examined the effects
of exogenous FABP4 on human prostate cancer cell progression. FABP4 treatment promoted serum-induced prostate cancer cell invasion in vitro. Furthermore, oleic acid promoted prostate cancer cell
invasion only if FABP4 was present in the medium. These promoting
effects were reduced by FABP4 inhibitor, which inhibits FABP4 binding to
fatty acids. Immunostaining for FABP4 showed that exogenous FABP4 was
taken up into DU145 cells in three-dimensional culture. In mice,
treatment with FABP4 inhibitor reduced the subcutaneous growth and lung
metastasis of prostate cancer cells. Immunohistochemical analysis showed
that the number of apoptotic cells, positive for cleaved caspase-3 and
cleaved PARP, was increased in subcutaneous tumors of FABP4
inhibitor-treated mice, as compared with control mice. These results
suggest that exogenous FABP4 might promote human prostate cancer cell progression by binding with fatty acids. Additionally, exogenous FABP4 activated the PI3K/Akt pathway,
independently of binding to fatty acids. Thus, FABP4 might be a key
molecule to understand the mechanisms underlying the obesity-prostate
cancer progression link.
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