Evidence map›Paper›PMID 16188329›Full record

ArticleAntiviral research2005

Human cytomegalovirus-inhibitory flavonoids: studies on antiviral activity and mechanism of action.

David L Evers, Chih-Fang Chao, Xin Wang, Zhigang Zhang, Shu-Mei Huong, Eng-Shang Huang

Abstract read
In one paragraph

Article in Antiviral research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

58 citing papers in PubMed, 155 citations in OpenAlex.

  1. Latin American Plants against Microorganisms.Plants (Basel, Switzerland) · 2023
    Review
  2. Article
  3. Article
  4. Anti-CMV therapy, what next? A systematic review.Frontiers in microbiology · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Review
  10. Article
  11. Article
  12. Natural products can be used in therapeutic management of COVID-19: Probable mechanistic insights.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Review
  13. Focus on the high therapeutic potentials of quercetin and its derivatives.Phytomedicine plus : international journal of phytotherapy and phytopharmacology · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Effects of Nelumbo nucifera Leaf Extract on Obesity.Plant foods for human nutrition (Dordrecht, Netherlands) · 2021
    Article
  20. 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

6 authors at 1 institution in 1 country.

David L EversLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, NC 27599-7295, USA.
Chih-Fang Chao
Xin Wang
Zhigang Zhang
Shu-Mei Huong
Eng-Shang Huang
University of North Carolina at Chapel Hill · US

Funding

Vironomics and Biostatistics CoreP01CA019014 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOSSOM A DAMANIA, NANCY JOAN RAAB-TRAUB · 1985 to 2026
$43.8M
Integrated Training in Cancer Model SystemsT32CA009156 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DER, CHANNING J. · 1985 to 2020
$19.7M
HCMV IN AIDS--DISRUPTION OF CELL CYCLE REGULATIONR01AI047678 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI HUANG, ENG-SHANG · 2000 to 2004
$1.3M
NCI NIH HHS CA09156NCI NIH HHS CA19014NCI NIH HHS P01 CA019014NCI NIH HHS T32 CA009156NIAID NIH HHS AI47678NIAID NIH HHS R01 AI047678
6 · The paper itself

Abstract

We report antiviral activity against human cytomegalovirus for certain dietary flavonoids and their likely biochemical mechanisms of action. Nine out of ten evaluated flavonoids blocked HCMV replication at concentrations that were significantly lower than those producing cytotoxicity against growing or stationary phase host cells. Baicalein was the most potent inhibitor in this series (IC(50)=0.4-1.2 microM), including positive control ganciclovir. Baicalein and genistein were chosen as model compounds to study the antiviral mechanism(s) of action for this series. Both flavonoids significantly reduced the levels of HCMV early and late proteins, as well as viral DNA synthesis. Baicalein reduced the levels of HCMV immediate-early proteins to nearly background levels while genistein did not. The antiviral effects of genistein, but not baicalein, were fully reversible in cell culture. Pre-incubation of concentrated virus stocks with either flavonoid did not inhibit HCMV replication, suggesting that baicalein did not directly inactivate virus particles. Baicalein functionally blocked epidermal growth factor receptor tyrosine kinase activity and HCMV nuclear translocation, while genistein did not. At 24h post infection HCMV-infected cells treated with genistein continued to express immediate-early proteins and efficiently phosphorylate IE1-72. However, HCMV induction of NF-kappaB and increases in the levels of cell cycle regulatory proteins--events that are associated with immediate-early protein functioning--were absent. The data suggested that the primary mechanism of action for baicalein may be to block HCMV infection at entry while the primary mechanism of action for genistein may be to block HCMV immediate-early protein functioning.

Indexed as

Antiviral AgentsCell Culture TechniquesCytomegalovirusFlavonoidsHumansImmediate-Early ProteinsVirus ReplicationAntiviral AgentsFlavonoidsImmediate-Early Proteins

Identifiers

PMID16188329
PMCPMC7114262
OpenAlexW1979411899

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.