Evidence map›Paper›PMID 27502288›Full record

ReviewFuture medicinal chemistry2016

Sphingolipids as targets for treatment of fungal infections.

Rodrigo Rollin-Pinheiro, Ashutosh Singh, Eliana Barreto-Bergter, Maurizio Del Poeta

Abstract readReview
In one paragraph

Review in Future medicinal chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

46 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Review
  3. The antimicrobial activity of ETD151 defensin is dictated by the presence of glycosphingolipids in the targeted organisms.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Regulation of cellular and systemic sphingolipid homeostasis.Nature reviews. Molecular cell biology · 2024
    Review
  5. Antifungal Activity of Disalt of Epipyrone A fromJournal of fungi (Basel, Switzerland) · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Role of sphingolipids in the host-pathogen interaction.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Identification of Promising Antifungal Drugs againstJournal of fungi (Basel, Switzerland) · 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

4 authors at 2 institutions in 2 countries.

Rodrigo Rollin-PinheiroDepartamento de Microbiologia Geral, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, UFRJ, 21941-902 Rio de Janeiro, Brazil.
Ashutosh SinghDepartment of Molecular Genetics & Microbiology, Stony Brook University, 145 Life Sciences Building, Stony Brook, 11794 NY, USA.
Eliana Barreto-BergterDepartamento de Microbiologia Geral, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, UFRJ, 21941-902 Rio de Janeiro, Brazil.
Maurizio Del PoetaDepartment of Molecular Genetics & Microbiology, Stony Brook University, 145 Life Sciences Building, Stony Brook, 11794 NY, USA.
Stony Brook University · USUniversidade Federal do Rio de Janeiro · BR

Funding

New antifungals targeting the synthesis of fungal sphingolipidsR01AI116420 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI Maurizio Del Poeta · 2016 to 2026
$7.6M
Sphingolipid-mediated fungal pathogenesisR01AI056168 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI DEL POETA, MAURIZIO · 2004 to 2013
$2.7M
Identification of new compounds against fungal microbesR21AI100631 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI DEL POETA, MAURIZIO · 2013 to 2014
$425k
Role of host spingolipids against fungal infectionsI01BX002624 · VA · NORTHPORT VA MEDICAL CENTER · PI Maurizio Del Poeta · 2016 to 2026
–
BLRD VA I01 BX002624NIAID NIH HHS R01 AI056168NIAID NIH HHS R01 AI116420NIAID NIH HHS R21 AI100631
6 · The paper itself

Abstract

Invasive fungal infections have significantly increased in the last few decades. Three classes of drugs are commonly used to treat these infections: polyenes, azoles and echinocandins. Unfortunately each of these drugs has drawbacks; polyenes are toxic, resistance against azoles is emerging and echinocandins have narrow spectrum of activity. Thus, the development of new antifungals is urgently needed. In this context, fungal sphingolipids have emerged as a potential target for new antifungals, because their biosynthesis in fungi is structurally different than in mammals. Besides, some fungal sphingolipids play an important role in the regulation of virulence in a variety of fungi. This review aims to highlight the diverse strategies that could be used to block the synthesis or/and function of fungal sphingolipids.

Indexed as

Antifungal AgentsFungiHumansMicrobial Sensitivity TestsMolecular StructureMycosesSphingolipidsVirulenceAntifungal AgentsSphingolipidsantifungalsdrugsfungiglucosylceramidesphingolipidstargets

Identifiers

PMID27502288
PMCPMC5558548
OpenAlexW2515580787

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.