Evidence map›Paper›PMID 18191976›Full record

ArticleVirology2008

Curcumin inhibits herpes simplex virus immediate-early gene expression by a mechanism independent of p300/CBP histone acetyltransferase activity.

Sebla B Kutluay, James Doroghazi, Martha E Roemer, Steven J Triezenberg

Open access · greenAbstract read
In one paragraph

Article in Virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 173 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Advancements in the development of antivirals against SARS-Coronavirus.Frontiers in cellular and infection microbiology · 2025
    Review
  6. Article
  7. Potential of Curcumin in the Management of Skin Diseases.International journal of molecular sciences · 2024
    Review
  8. Promising Potential of Curcumin and Related Compounds for Antiviral Drug Discovery.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Polyphenols as Potent Epigenetics Agents for Cancer.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Pulsed blue light, saliva and curcumin significantly inactivate human coronavirus.Journal of photochemistry and photobiology. B, Biology · 2022
    Article
  20. Review

5 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

4 authors at 2 institutions in 1 country.

Sebla B KutluayGraduate Program in Cell and Molecular Biology, Michigan State University, East Lansing, MI 48824, USA.
James Doroghazi
Martha E Roemer
Steven J Triezenberg
Van Andel Institute · USMichigan State University · US

Funding

Chromatin and Coactivators in HSV-1 gene regulationR01AI064634 · NIAID · VAN ANDEL RESEARCH INSTITUTE · PI TRIEZENBERG, STEVEN J. · 2007 to 2009
$1.1M
NIAID NIH HHS R01 AI064634
6 · The paper itself

Abstract

Curcumin, a phenolic compound from the curry spice turmeric, exhibits a wide range of activities in eukaryotic cells, including antiviral effects that are at present incompletely characterized. Curcumin is known to inhibit the histone acetyltransferase activity of the transcriptional coactivator proteins p300 and CBP, which are recruited to the immediate early (IE) gene promoters of herpes simplex virus type 1 (HSV-1) by the viral transactivator protein VP16. We tested the hypothesis that curcumin, by inhibiting these coactivators, would block viral infection and gene expression. In cell culture assays, curcumin significantly decreased HSV-1 infectivity and IE gene expression. Entry of viral DNA to the host cell nucleus and binding of VP16 to IE gene promoters was not affected by curcumin, but recruitment of RNA polymerase II to those promoters was significantly diminished. However, these effects were observed using lower curcumin concentrations than those required to substantially inhibit global H3 acetylation. No changes were observed in histone H3 occupancy or acetylation at viral IE gene promoters. Furthermore, p300 and CBP recruitment to IE gene promoters was not affected by the presence of curcumin. Finally, disruption of p300 expression using a short hairpin RNA did not affect viral IE gene expression. These results suggest that curcumin affects VP16-mediated recruitment of RNA polymerase II to IE gene promoters by a mechanism independent of p300/CBP histone acetyltransferase activity.

Indexed as

Active Transport, Cell NucleusAnimalsBase SequenceChlorocebus aethiopsChromatin ImmunoprecipitationCurcuminDNA PrimersGene ExpressionGenes, Immediate-EarlyGenes, ViralGenome, ViralHeLa CellsHerpes Simplex Virus Protein Vmw65Herpesvirus 1, HumanHumansOpen Reading FramesCurcuminDNA PrimersHerpes Simplex Virus Protein Vmw65p300-CBP Transcription FactorsRNA Polymerase II

Identifiers

PMID18191976
PMCPMC2668156
OpenAlexW1972837337

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.