Evidence map›Paper›PMID 35354596›Full record

ArticleLife science alliance2022

ESCRT-I fuels lysosomal degradation to restrict TFEB/TFE3 signaling via the Rag-mTORC1 pathway.

Marta Wróbel, Jarosław Cendrowski, Ewelina Szymańska, Malwina Grębowicz-Maciukiewicz, Noga Budick-Harmelin, Matylda Macias, Aleksandra Szybińska, Michał Mazur, Krzysztof Kolmus, Krzysztof Goryca and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Life science alliance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Marta WróbelLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0003-4939-6299
Jarosław CendrowskiLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland miaczynska@iimcb.gov.pl jcendrowski@iimcb.gov.pl.ORCID 0000-0002-8579-7279
Ewelina SzymańskaLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0001-7994-0764
Malwina Grębowicz-MaciukiewiczLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0002-9012-5434
Noga Budick-HarmelinLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.
Matylda MaciasMicroscopy and Cytometry Facility, International Institute of Molecular and Cell Biology, Warsaw, Poland.
Aleksandra SzybińskaMicroscopy and Cytometry Facility, International Institute of Molecular and Cell Biology, Warsaw, Poland.
Michał MazurLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.
Krzysztof KolmusLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0002-9155-6383
Krzysztof GorycaDepartment of Genetics, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Michalina DąbrowskaDepartment of Genetics, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Agnieszka PaziewskaDepartment of Gastroenterology, Hepatology and Clinical Oncology, Medical Center for Postgraduate Education, Warsaw, Poland.
Michał MikulaDepartment of Genetics, Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Marta MiączyńskaLaboratory of Cell Biology, International Institute of Molecular and Cell Biology, Warsaw, Poland miaczynska@iimcb.gov.pl jcendrowski@iimcb.gov.pl.ORCID 0000-0003-0031-5267
International Institute of Molecular and Cell Biology · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLPostgraduate School of Molecular Medicine · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Within the endolysosomal pathway in mammalian cells, ESCRT complexes facilitate degradation of proteins residing in endosomal membranes. Here, we show that mammalian ESCRT-I restricts the size of lysosomes and promotes degradation of proteins from lysosomal membranes, including MCOLN1, a Ca

Indexed as

Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsEndosomal Sorting Complexes Required for TransportAnimalsLysosomesMammalsMechanistic Target of Rapamycin Complex 1Signal TransductionBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsEndosomal Sorting Complexes Required for TransportMechanistic Target of Rapamycin Complex 1

Identifiers

PMID35354596
PMCPMC8967991
OpenAlexW4220718943

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.