Evidence map›Paper›PMID 30576108›Full record

ArticleACS chemical biology2019

Transient Compound Treatment Induces a Multigenerational Reduction of Oxysterol-Binding Protein (OSBP) Levels and Prophylactic Antiviral Activity.

Brett L Roberts, Zachary C Severance, Ryan C Bensen, Anh T Le, Naga Rama Kothapalli, Juan I Nuñez, Hongyan Ma, Si Wu, Shawna J Standke, Zhibo Yang and 3 more

Abstract read
In one paragraph

Article in ACS chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. 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
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Enterovirus A71 antivirals: Past, present, and future.Acta pharmaceutica Sinica. B · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
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

13 authors at 2 institutions in 1 country.

Brett L RobertsDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Zachary C SeveranceDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Ryan C BensenDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Anh T LeDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Naga Rama KothapalliDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Juan I NuñezDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Hongyan MaDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Si WuDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Shawna J StandkeDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
Zhibo YangDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.ORCID 0000-0003-0370-7450
William J ReddigDepartment of Biochemistry and Microbiology , Oklahoma State University Center for Health Sciences , 1111 West 17th Street , Tulsa , Oklahoma 74107 , United States.
Earl L BlewettDepartment of Biochemistry and Microbiology , Oklahoma State University Center for Health Sciences , 1111 West 17th Street , Tulsa , Oklahoma 74107 , United States.
Anthony W G BurgettDepartment of Chemistry and Biochemistry , The University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.ORCID 0000-0002-0685-5144
University of Oklahoma · USOklahoma State University Center for Health Sciences · US

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
From Single Cells to Tissues: a Novel Mass Spectrometry Approach for BioanalysisR01GM116116 · NIGMS · UNIVERSITY OF OKLAHOMA · PI YANG, ZHIBO · 2015 to 2019
$1.5M
Mass Spectrometry Detection of Drugs in Single Bladder Cancer Cells from PatientsR21CA204706 · NCI · UNIVERSITY OF OKLAHOMA · PI BURGETT, ANTHONY WG · 2016 to 2018
$599k
NCI NIH HHS R21 CA204706NIGMS NIH HHS R01 GM116116NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

Oxysterol-binding protein (OSBP) is a lipid transport and regulatory protein required for the replication of Enterovirus genus viruses, which includes many significant human pathogens. Short-term exposure (i.e., 1-6 h) to a low dose (i.e., 1 nM) of the natural product compound OSW-1 induces a reduction of cellular OSBP levels by ∼90% in multiple different cell lines with no measurable cytotoxicity, defect in cellular proliferation, or global proteome reduction. Interestingly, the reduction of OSBP levels persists multiple days after the low-dose, transient OSW-1 compound treatment is ended and the intracellular OSW-1 compound levels drop to undetectable levels. The reduction in OSBP levels is inherited in multiple generations of cells that are propagated after the OSW-1 compound treatment is stopped. The enduring multiday, multigenerational reduction of OSBP levels triggered by the OSW-1 compound is not due to proteasome degradation of OSBP or due to a reduction in OSBP mRNA levels. OSW-1 compound treatment induces transient autophagy in cells, but blocking autophagy does not rescue OSBP levels. Although the specific cellular mechanism of long-term OSBP repression is not yet identified, these results clearly show the existence of an OSBP specific cellular regulation process that is triggered upon treatment with an OSBP-binding compound. The stable reduction of OSBP levels upon short-term, transient OSW-1 compound treatment will be a powerful tool to understand OSBP regulation and cellular function. Additionally, the persistent reduction in OSBP levels triggered by the transient OSW-1 compound treatment substantially reduces viral replication in treated cells. Therefore, the long-term, compound-induced reduction of OSBP in cells presents a new route to broad spectrum anti- Enterovirus activity, including as a novel route to antiviral prophylactic treatment through small molecule targeting a human host protein.

Indexed as

Antiviral AgentsDose-Response Relationship, DrugEnterovirusHumansOxysterol Binding ProteinsReceptors, SteroidViral ProteinsVirus ReplicationAntiviral AgentsOxysterol Binding ProteinsReceptors, SteroidViral Proteins

Identifiers

PMID30576108
PMCPMC6379863
OpenAlexW2905633689

What OpenQuestion holds

Textmetadata
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.