Evidence map›Paper›PMID 24606695›Full record

ArticleVirology2014

mTOR/p70S6K signaling distinguishes routine, maintenance-level autophagy from autophagic cell death during influenza A infection.

Emmanuel Datan, Alireza Shirazian, Shawna Benjamin, Demetrius Matassov, Antonella Tinari, Walter Malorni, Richard A Lockshin, Adolfo Garcia-Sastre, Zahra Zakeri

Abstract read
In one paragraph

Article in Virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.4field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

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  15. Decanoic acid inhibits mTORC1 activity independent of glucose and insulin signaling.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  16. The Dephosphorylation of p70S6 (ThrNeurotoxicity research · 2020
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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

9 authors at 3 institutions in 2 countries.

Emmanuel DatanDepartment of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Alireza Shirazian *Department of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Shawna Benjamin *Department of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Demetrius MatassovDepartment of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Antonella TinariDepartment of Technology and Health, Instituto Superiore di Sanita, Viale Regina Elena 299, 00161 Rome, Italy.
Walter MalorniDepartment of Drug Research and Evaluation, Instituto Superiore di Sanita, Viale Regina Elena 299, 00161 Rome, Italy.
Richard A LockshinDepartment of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Adolfo Garcia-SastreDepartment of Microbiology, Division of Infectious Diseases, Mount Sinai School of Medicine, New York, NY 10029, USA.
Zahra ZakeriDepartment of Biology, Queens College and Graduate Center of the City University of New York, 65-30 Kissena Boulevard, Flushing, NY 11367, USA.
Queens College, CUNY · USIstituto Superiore di Sanità · ITIcahn School of Medicine at Mount Sinai · US

Funding

MARC Undergraduate Student Training in Academic Research at Queens CollegeT34GM070387 · NIGMS · QUEENS COLLEGE · PI ZAKERI, ZAHRA · 2004 to 2021
$6.8M
Characterization of flavovirus NS4A induced autophagyR15AI094351 · NIAID · QUEENS COLLEGE · PI ZAKERI, ZAHRA · 2011 to 2017
$459k
NIAID NIH HHS R15 AI094351NIGMS NIH HHS T34 GM070387NIGMS NIH HHS T34GM070387PHS HHS 1R15AIO94351-01
6 · The paper itself

Abstract

Autophagy, a stress response activated in influenza A virus infection helps the cell avoid apoptosis. However, in the absence of apoptosis infected cells undergo vastly expanded autophagy and nevertheless die in the presence of necrostatin but not of autophagy inhibitors. Combinations of inhibitors indicate that the controls of protective and lethal autophagy are different. Infection that triggers apoptosis also triggers canonical autophagy signaling exhibiting transient PI3K and mTORC1 activity. In terminal autophagy phospho-mTOR(Ser2448) is suppressed while mTORC1, PI3K and mTORC2 activities increase. mTORC1 substrate p70S6K becomes highly phosphorylated while its activity, now regulated by mTORC2, is required for LC3-II formation. Inhibition of mTORC2/p70S6K, unlike that of PI3K/mTORC1, blocks expanded autophagy in the absence of apoptosis but not moderate autophagy. Inhibitors of expanded autophagy limit virus reproduction. Thus expanded, lethal autophagy is activated by a signaling mechanism different from autophagy that helps cells survive toxic or stressful episodes.

Indexed as

AutophagySignal TransductionApoptosisHumansInfluenza A virusInfluenza, HumanMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesPhosphatidylinositol 3-KinasesRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine KinasesMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesPhosphatidylinositol 3-KinasesRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine KinasesApoptosisAutophagyCell deathInfluenzamTORC1/2p70S6KRapamycinTorin1

Identifiers

PMID24606695
PMCPMC4005847
OpenAlexW2008553918

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.