Evidence map›Paper›PMID 26526588›Full record

ReviewAntiviral research2015

Targeting host lipid synthesis and metabolism to inhibit dengue and hepatitis C viruses.

Valerie A Villareal, Mary A Rodgers, Deirdre A Costello, Priscilla L Yang

Open access · greenAbstract readReview
In one paragraph

Review in Antiviral research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

45 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  14. Plasmalogen Loss in Sepsis and SARS-CoV-2 Infection.Frontiers in cell and developmental biology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Statins in COVID-19 Therapy.Life (Basel, Switzerland) · 2021
    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

4 authors at 1 institution in 1 country.

Valerie A VillarealDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.
Mary A RodgersDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.
Deirdre A CostelloDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.
Priscilla L YangDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA. Electronic address: priscilla_yang@hms.harvard.edu.
Harvard University · US

Funding

Small-molecule inhibitors of flavivirus entryU19AI109740 · NIAID · HARVARD MEDICAL SCHOOL · PI WHELAN, SEAN PJ · 2014 to 2018
$23.0M
Validation of Src kinases as Anti-Dengue Viral TargetsR01AI076442 · NIAID · HARVARD MEDICAL SCHOOL · PI YANG, PRISCILLA LI-NING · 2008 to 2012
$2.1M
Chemical Tools for the Study of Dengue Virus EntryR01AI095499 · NIAID · HARVARD MEDICAL SCHOOL · PI GRAY, NATHANAEL SCHIANDER, YANG, PRISCILLA LI-NING · 2014 to 2016
$1.3M
Negative Regulation of NLRP1-inflammasomes by the linear ubiquitin assembly complF32AI096698 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RODGERS, MARY · 2011 to 2013
$155k
Mechanistic Studies of the Function of Desmosterol Homeostasis in HCV ReplicationF32AI106178 · NIAID · HARVARD MEDICAL SCHOOL · PI VILLAREAL, VALERIE ANNE AGUSTINO · 2013 to 2015
$151k
NIAID NIH HHS F32 AI096698NIAID NIH HHS F32-AI096698NIAID NIH HHS F32 AI106178NIAID NIH HHS F32AI106178NIAID NIH HHS R01 AI076442NIAID NIH HHS R01AI076442NIAID NIH HHS R01 AI095499NIAID NIH HHS U19 AI109740NIAID NIH HHS U19AI109740
6 · The paper itself

Abstract

Lipids are necessary for every step in the replication cycle of hepatitis C virus (HCV) and dengue virus (DENV), members of the family Flaviviridae. Recent studies have demonstrated that discrete steps in the replication cycles of these viruses can be inhibited by pharmacological agents that target host factors mediating lipid synthesis, metabolism, trafficking, and signal transduction. Despite this, targeting host lipid metabolism and trafficking as an antiviral strategy by blockade of entire pathways may be limited due to host toxicity. Knowledge of the molecular details of lipid structure and function in replication and the mechanisms whereby specific lipids are generated and trafficked to the relevant sites may enable more targeted antiviral strategies without global effects on the host cell. In this review, we discuss lipids demonstrated to be critical to the replication cycles of HCV and DENV and highlight potential areas for anti-viral development. This review article forms part of a symposium on flavivirus drug discovery in Antiviral Research.

Indexed as

Molecular Targeted TherapyAntiviral AgentsDengueDengue VirusDrug DiscoveryHepacivirusHepatitis CHost-Pathogen InteractionsHumansLipid MetabolismLipidsSignal TransductionVirus ReplicationAntiviral AgentsLipidsAntiviral therapyDengue virusFlavivirusHepatitis C virusHost-targeted antiviralLipids

Identifiers

PMID26526588
PMCPMC4699661
OpenAlexW1922641266

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.