Evidence map›Paper›PMID 26958925›Full record

ReviewAnnual review of virology2015

Pathophysiological Consequences of Calcium-Conducting Viroporins.

Joseph M Hyser, Mary K Estes

Open access · bronzeAbstract readReview
In one paragraph

Review in Annual review of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
1.3field-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, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Pooled it
  2. Transient receptor potential channels inChannels (Austin, Tex.) · 2026
    Review
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  18. Host IPmBio · 2024
    Article
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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

2 authors at 2 institutions in 2 countries.

Joseph M HyserAlkek Center for Metagenomic and Microbiome Research.
Mary K EstesDepartment of Molecular Virology and Microbiology, and.
Baylor College of Medicine · USInstitute of Metagenomics and Microbial Technologies (Slovenia) · SI

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI James Versalovic · 2001 to 2026
$28.3M
Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI KLINE, MARK W. · 1994 to 2015
$21.7M
TRANSGENIC MOUSE MODELS TO STUDY OVARIAN FUNCTIONU54HD007495 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MATZUK, MARTIN M. · 1998 to 2013
$19.9M
Regulation of Rotavirus ReplicationR01AI080656 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI Sue Ellen Crawford, Mary Kolb Estes · 2009 to 2026
$7.9M
Enteric Virus Calcium Channel InhibitorsK01DK093657 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI HYSER, JOSEPH M. · 2012 to 2016
$639k
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
Regulation of Enteric Virus Secretory DiarrheaR03DK110270 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI HYSER, JOSEPH M. · 2017 to 2018
$159k
NCI NIH HHS CA125123NCI NIH HHS P30 CA125123NCI NIH HHS P30CA125123NCRR NIH HHS RR024574NCRR NIH HHS S10 RR024574NIAID NIH HHS AI036211NIAID NIH HHS P30 AI036211NIAID NIH HHS R01 AI080656NIAID NIH HHS R01AI080656NICHD NIH HHS U54 HD007495NICHD NIH HHS U54HD007495NIDDK NIH HHS K01 DK093657NIDDK NIH HHS K01DK093657NIDDK NIH HHS P30 DK056338NIDDK NIH HHS P30DK56338,NIDDK NIH HHS R03 DK110270
6 · The paper itself

Abstract

Eukaryotic cells have evolved a myriad of ion channels, transporters, and pumps to maintain and regulate transmembrane ion gradients. As intracellular parasites, viruses also have evolved ion channel proteins, called viroporins, which disrupt normal ionic homeostasis to promote viral replication and pathogenesis. The first viral ion channel (influenza M2 protein) was confirmed only 23 years ago, and since then studies on M2 and many other viroporins have shown they serve critical functions in virus entry, replication, morphogenesis, and immune evasion. As new candidate viroporins and viroporin-mediated functions are being discovered, we review the experimental criteria for viroporin identification and characterization to facilitate consistency within this field of research. Then we review recent studies on how the few Ca(2+)-conducting viroporins exploit host signaling pathways, including store-operated Ca(2+) entry, autophagy, and inflammasome activation. These viroporin-induced aberrant Ca(2+) signals cause pathophysiological changes resulting in diarrhea, vomiting, and proinflammatory diseases, making both the viroporin and host Ca(2+) signaling pathways potential therapeutic targets for antiviral drugs.

Indexed as

AnimalsCalciumHumansIon ChannelsViral ProteinsVirus DiseasesVirusesCalciumIon ChannelsViral Proteinsautophagycalcium homeostasisinflammasomestore-operated calcium entryviroporin

Identifiers

PMID26958925
PMCPMC6538290
OpenAlexW2150112131

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.