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Fuligocandin B () is a novel natural product that can overcome TRAIL resistance. We synthesized enatiomerically pure fuligocandin B () and its derivative 5'-I fuligocandin B (), and found that the latter had an improved biological activity against the human gastric cancer cell line, AGS. We attached a biotin linker and photoactivatable aryl diazirine group to 5'-I fuligocandin B (), and employed a pull-down assay to identify valosin-containing protein (VCP/p97), an AAA ATPase, as a 5'-I fuligocandin B () target protein. Knock-down of VCP by siRNA enhanced sensitivity to TRAIL in AGS cells. In addition, enhanced CHOP and DR5 protein expression, and overall intracellular levels of ubiquitinated protein. These data suggest that endoplasmic reticulum stress caused through VCP inhibition by increases CHOP-mediated DR5 up-regulation, which enhances TRAIL-induced cell death in AGS cells. To the best of our knowledge, this is the first example to show a relationship between VCP and TRAIL-resistance-overcoming activity in cancer cells.
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http://dx.doi.org/10.1002/open.201600081 | DOI Listing |
ChemistryOpen
December 2016
Graduate School of Pharmaceutical Sciences Chiba University 1-8-1 Inohana, Chuo-ku Chiba 260-8675 Japan.
Fuligocandin B () is a novel natural product that can overcome TRAIL resistance. We synthesized enatiomerically pure fuligocandin B () and its derivative 5'-I fuligocandin B (), and found that the latter had an improved biological activity against the human gastric cancer cell line, AGS. We attached a biotin linker and photoactivatable aryl diazirine group to 5'-I fuligocandin B (), and employed a pull-down assay to identify valosin-containing protein (VCP/p97), an AAA ATPase, as a 5'-I fuligocandin B () target protein.
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