Evidence map›Paper›PMID 21822274›Full record

ArticleNature chemical biology2011

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

Anthony W G Burgett, Thomas B Poulsen, Kittikhun Wangkanont, D Ryan Anderson, Chikako Kikuchi, Kousei Shimada, Shuichi Okubo, Kevin C Fortner, Yoshihiro Mimaki, Minpei Kuroda and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature chemical biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
13.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

113 citing papers in PubMed, 258 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Role of Oxysterol-Binding Protein Family in Cholesterol Metabolism and Cancer Progression: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Advanced RPL19-TRAPNatural products and bioprospecting · 2025
    Article
  16. All roads lead to OSBP.Nature chemical biology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Molecular biology of the cell · 2025
    Article

53 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 3 countries.

Anthony W G BurgettDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, USA.
Thomas B Poulsen
Kittikhun Wangkanont
D Ryan Anderson
Chikako Kikuchi
Kousei Shimada
Shuichi Okubo
Kevin C Fortner
Yoshihiro Mimaki
Minpei Kuroda
Jason P Murphy
David J Schwalb
Eugene C Petrella
Ivan Cornella-Taracido
Markus Schirle
John A Tallarico
Matthew D Shair
Harvard University · USNovartis (United States) · USNovartis (Switzerland) · CHTokyo University of Pharmacy and Life Sciences · JP

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Chemical Biology Studies of Human Disease-Relevant Small MoleculesR01GM090068 · NIGMS · HARVARD UNIVERSITY · PI SHAIR, MATTHEW D. · 2010 to 2013
$1.6M
NCRR NIH HHS UL1 RR025758NCRR NIH HHS UL1RR025758NIGMS NIH HHS R01 GM090068NIGMS NIH HHS R01GM090068
6 · The paper itself

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.

Indexed as

Biological ProductsCarrier ProteinsCell Line, TumorCell ProliferationCholestenonesHumansHydroxycholesterolsLipid MetabolismNeoplasmsOxysterol Binding ProteinsPhenazinesReceptors, SteroidSaponinsSignal TransductionSphingomyelinsSpiro Compounds25-hydroxycholesterolBiological ProductsCarrier Proteinscephalostatin ICholestenonesHydroxycholesterolsOSW 1Oxysterol Binding ProteinsPhenazinesReceptors, Steroidritterazine BSaponinsschweinfurthinSphingomyelinsSpiro CompoundsSteroidsStilbenes

Identifiers

PMID21822274
PMCPMC3158287
OpenAlexW1996878278

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.