Evidence map›Paper›PMID 32998777›Full record

ReviewLipids in health and disease2020

Signaling and other functions of lipids in autophagy: a review.

Alejandro Soto-Avellaneda, Brad E Morrison

Abstract readReview
In one paragraph

Review in Lipids in health and disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

39 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Alejandro Soto-AvellanedaBiomolecular Sciences Graduate programs, Boise State University, Boise, ID, 83725, USA.ORCID http://orcid.org/0000-0003-2600-9639
Brad E MorrisonBiomolecular Sciences Graduate programs, Boise State University, Boise, ID, 83725, USA. bradmorrison@boisestate.edu.

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Carolyn Hovde Bohach · 2012 to 2026
$59.8M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
Autophagy dysfunction in Parkinson's Disease by VPS35 D620NR15NS096702 · NINDS · BOISE STATE UNIVERSITY · PI MORRISON, BRAD · 2016 to 2017
$521k
NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P20GM103408NIGMS NIH HHS P20 GM109095NIGMS NIH HHS P20GM109095NINDS NIH HHS R15 NS096702NINDS NIH HHS R15NS096702
6 · The paper itself

Abstract

The process of autophagy is integral to cellular function. In this process, proteins, organelles, and metabolites are engulfed in a lipid vesicle and trafficked to a lysosome for degradation. Its central role in protein and organelle homeostasis has piqued interest for autophagy dysfunction as a driver of pathology for a number of diseases including cancer, muscular disorders, neurological disorders, and non-alcoholic fatty liver disease. For much of its history, the study of autophagy has centered around proteins, however, due to advances in mass spectrometry and refined methodologies, the role of lipids in this essential cellular process has become more apparent. This review discusses the diverse endogenous lipid compounds shown to mediate autophagy. Downstream lipid signaling pathways are also reviewed in the context of autophagy regulation. Specific focus is placed upon the Mammalian Target of Rapamycin (mTOR) and Peroxisome Proliferator-Activated Receptor (PPAR) signaling pathways as integration hubs for lipid regulation of autophagy.

Indexed as

AutophagyHomeostasisHumansLipidsLysosomesPeroxisome Proliferator-Activated ReceptorsProtein TransportSignal TransductionTOR Serine-Threonine KinasesLipidsMTOR protein, humanPeroxisome Proliferator-Activated ReceptorsTOR Serine-Threonine KinasesAutophagyFatty acidsLipidsMammalian target of rapamycinPeroxisome proliferator-activated receptorPhospholipidsSphingolipids

Identifiers

PMID32998777
PMCPMC7525950

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.