0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Natural products reveal cancer cell dependence on oxysterol-binding proteins.

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cephalostatin 1, OSW-1, ritterazine B and schweinfurthin A are natural products that potently, and in some cases selectively, inhibit the growth of cultured human cancer cell lines. The cellular targets of these small molecules have yet to be identified. We have discovered that these molecules target oxysterol binding protein (OSBP) and its closest paralog, OSBP-related protein 4L (ORP4L)--proteins not known to be involved in cancer cell survival. OSBP and the ORPs constitute an evolutionarily conserved protein superfamily, members of which have been implicated in signal transduction, lipid transport and lipid metabolism. The functions of OSBP and the ORPs, however, remain largely enigmatic. Based on our findings, we have named the aforementioned natural products ORPphilins. Here we used ORPphilins to reveal new cellular activities of OSBP. The ORPphilins are powerful probes of OSBP and ORP4L that will be useful in uncovering their cellular functions and their roles in human diseases.

          Related collections

          Author and article information

          Journal
          Nat Chem Biol
          Nature chemical biology
          Springer Science and Business Media LLC
          1552-4469
          1552-4450
          Aug 07 2011
          : 7
          : 9
          Affiliations
          [1 ] Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, USA.
          Article
          nchembio.625 NIHMS317449
          10.1038/nchembio.625
          3158287
          21822274
          f52aa818-65e7-4393-89e2-e94ecb1b1479
          History

          Comments

          Comment on this article