Evidence map›Paper›PMID 18625767›Full record

ArticleAntimicrobial agents and chemotherapy2008

Heterocyclic compounds that inhibit Rev-RRE function and human immunodeficiency virus type 1 replication.

Deidra Shuck-Lee, Fei Fei Chen, Ryan Willard, Sharmila Raman, Roger Ptak, Marie-Louise Hammarskjold, David Rekosh

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2008. 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
0.3field-weighted citation impact, top 47% 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, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 1Molecules (Basel, Switzerland) · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Small molecules targeting viral RNA.Wiley interdisciplinary reviews. RNA · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

7 authors at 2 institutions in 1 country.

Deidra Shuck-LeeDepartment of Microbiology, Myles H Thaler Center for AIDS and Human Retrovirus Research, University of Virginia, Charlottesville, Virginia 22908, USA.
Fei Fei Chen
Ryan Willard
Sharmila Raman
Roger Ptak
Marie-Louise Hammarskjold
David Rekosh
University of Virginia · USSouthern Research Institute · US

Funding

Engineered gp41 Peptides as HIV-1 Topical MicrobicidesR01AI068591 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI LU, MIN · 2006 to 2009
$1.6M
Sam 68 and the Function of Mason Pfizer Monkey Virus CTER01CA097095 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HAMMARSKJOLD, MARIE-LOUISE · 2003 to 2007
$1.5M
HIV Rev FunctionR01AI054335 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HAMMARSKJOLD, MARIE-LOUISE · 2003 to 2007
$1.5M
HIV Rev as a Therapeutic TargetR21AI054213 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI REKOSH, DAVID M · 2002 to 2003
$444k
NCI NIH HHS CA097095NCI NIH HHS R01 CA097095NIAID NIH HHS AI054213NIAID NIH HHS AI054335NIAID NIH HHS AI068591NIAID NIH HHS R01 AI054335NIAID NIH HHS R01 AI068591NIAID NIH HHS R21 AI054213
6 · The paper itself

Abstract

A cell-based screening assay was performed to identify compounds that inhibited the postintegration stage of the human immunodeficiency virus (HIV) life cycle. This assay utilized a cell line that contains the HIV gag and pol genes expressed in a Rev-dependent fashion. The cell line produces about 10 to 15 ng of p24 per milliliter of medium over a 24-h period in the form of viruslike particles. Any compound that inhibits a postintegration step in the HIV life cycle scores in this assay by decreasing particle production. Forty thousand compounds were screened, and 192 compounds were selected from the original screen because they showed more than 50% inhibition at a 10 muM concentration. The cumulative evidence presented in this study strongly suggests that 2 of the 192 compounds work as inhibitors of HIV Rev function. This was determined by a variety of cell-based assays, although the compounds do not interfere with Rev-RRE (Rev response element) binding in vitro. Both compounds inhibit replication of the lab isolate NL4-3 as well as an HIV primary isolate from Brazil (93BR021) and thus are promising leads as therapeutic candidates that target HIV replication through inhibition of Rev function.

Indexed as

AnimalsAnti-HIV AgentsCell LineChlorocebus aethiopsCOS CellsGene Products, revGenes, envHeterocyclic CompoundsHIV-1HIV InfectionsHumansLeukocytes, MononuclearMicrobial Sensitivity TestsVirus ReplicationAnti-HIV AgentsGene Products, revHeterocyclic Compounds

Identifiers

PMID18625767
PMCPMC2533482
OpenAlexW2147929308

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.