Evidence map›Paper›PMID 18666033›Full record

ReviewCurrent opinion in investigational drugs (London, England : 2000)2008

Signaling cascades as drug targets in model and pathogenic fungi.

Robert J Bastidas, Jennifer L Reedy, Helena Morales-Johansson, Joseph Heitman, Maria E Cardenas

Abstract readReview
In one paragraph

Review in Current opinion in investigational drugs (London, England : 2000), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Virulence Factors as Targets for Anticryptococcal Therapy.Journal of fungi (Basel, Switzerland) · 2016
    Review
  6. The Mechanistic Targets of Antifungal Agents: An Overview.Mini reviews in medicinal chemistry · 2016
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

5 authors at 1 institution in 1 country.

Robert J BastidasDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Research Drive, Box 3546, Durham, NC 27710, USA.
Jennifer L Reedy
Helena Morales-Johansson
Joseph Heitman
Maria E Cardenas
Duke University · US

Funding

Novel Antifungal Therapeutic ApproachesR01AI050438 · NIAID · DUKE UNIVERSITY · PI HEITMAN, JOSEPH · 2001 to 2012
$3.3M
Signaling mechanisms by the rapamycin target: Tor kinaseR01CA114107 · NCI · DUKE UNIVERSITY · PI CARDENAS-CORONA, MARIA E · 2005 to 2009
$1.3M
NCI NIH HHS R01 CA114107NIAID NIH HHS AI 50438NIAID NIH HHS R01 AI050438
6 · The paper itself

Abstract

Microbes evolved to produce natural products that inhibit growth of competing soil microorganisms. In many cases these compounds act on fungi, which are eukaryotes with conserved gene sequences closely related to metazoans, including humans. The calcineurin inhibitors cyclosporin A and FK-506, the Tor inhibitor rapamycin, and the Hsp90 inhibitor geldanamycin, all act via targets conserved from yeast to humans. This allows the use of genetically tractable fungi as models to elucidate how these drugs and their targets function in yeast and human cells. These inhibitors also enable studies aimed at harnessing their intrinsic antimicrobial activities to develop novel antifungal therapies. Extensive studies have revealed a globally conserved role for the Tor protein in regulating growth and proliferation in response to nutrients, and targeting its essential functions results in robust antifungal action. Similarly, a conserved and essential role for calcineurin in fungal virulence has been established and could be targeted by inhibitors for therapeutic uses in a variety of clinical settings. Finally, the discovery that inhibitors of calcineurin or Hsp90 result in dramatic synergism with either azoles or glucan synthase inhibitors (candins) provides another therapeutic vantage point. Taken together, these fungal targets and their inhibitors provide a robust platform from which to develop novel antimicrobial therapies.

Indexed as

Drug Delivery SystemsAntifungal AgentsCalcineurinCalcineurin InhibitorsHSP90 Heat-Shock ProteinsHumansMycosesProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsSignal TransductionAntifungal AgentsCalcineurinCalcineurin InhibitorsHSP90 Heat-Shock ProteinsProtein Serine-Threonine KinasesSaccharomyces cerevisiae Proteinstarget of rapamycin protein, S cerevisiae

Identifiers

PMID18666033
PMCPMC2715221
OpenAlexW38488696

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.