Evidence map›Paper›PMID 35188067›Full record

ArticleAutophagy2022

A dominant-negative regulatory mechanism of SQSTM1 droplets-based autophagy.

Evelina Valionyte, Elizabeth R Barrow, Chris R Baxter, Shouqing Luo

Open access · greenAbstract readComment
In one paragraph

Article in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Mechanisms Underlying Altitude-Induced and Group 3 Pulmonary Hypertension.International journal of molecular sciences · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Evelina ValionytePeninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK.
Elizabeth R BarrowPeninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK.
Chris R BaxterPeninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK.
Shouqing LuoPeninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK.ORCID 0000-0002-7998-3059
University of Plymouth · GB

Funding

Medical Research Council MR/M023605/1
6 · The paper itself

Abstract

SQSTM1/p62 is an autophagy receptor, forming droplets to sequester intracellular polyubiquitinated cargo and mediate its delivery for autophagic clearance. SQSTM1 droplets can function as platforms to allow the formation of autophagosomes at their surfaces. It would be interesting to understand how SQSTM1-droplet formation is regulated. We have shown that inflammatory toxicity induces SQSTM1 cleavage by CASP6 at a novel cleavage site, D256. The C-terminal cleavage product is unlikely to be functional, because it is hardly detectable, possibly due to its rapid turnover. The SQSTM1 N-terminal cleavage product (SQSTM1-N) exerts a dominant-negative effect on SQSTM1-droplet production, in turn attenuating SQSTM1 droplets-based autophagosome formation. Our study suggests that the CASP6-SQSTM1 axis negatively regulates SQSTM1 droplets-based autophagy under certain stress conditions.

Indexed as

AutophagosomesAutophagyMacroautophagySequestosome-1 ProteinSequestosome-1 ProteinAutophagosomesautophagyCASP6liquid dropletsSQSTM1

Identifiers

PMID35188067
PMCPMC9037419
OpenAlexW4213074275

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.