Evidence map›Paper›PMID 32424153›Full record

ArticleNature communications2020

TFEB regulates murine liver cell fate during development and regeneration.

Nunzia Pastore, Tuong Huynh, Niculin J Herz, Alessia Calcagni', Tiemo J Klisch, Lorenzo Brunetti, Kangho Ho Kim, Marco De Giorgi, Ayrea Hurley, Annamaria Carissimo and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. TFEB safeguards trophoblast syncytialization in humans and mice.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Lysosomes at the Crossroads of Cell Metabolism, Cell Cycle, and Stemness.International journal of molecular sciences · 2022
    Review
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

19 authors at 5 institutions in 3 countries.

Nunzia PastoreJan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA. pastore@tigem.it.ORCID http://orcid.org/0000-0002-8701-5592
Tuong HuynhJan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA.
Niculin J HerzJan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA.
Alessia Calcagni'Jan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0002-1946-5815
Tiemo J KlischJan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA.
Lorenzo BrunettiStem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0003-2624-8576
Kangho Ho KimDepartment of Molecular and Cell Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Marco De GiorgiDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, 77030, USA.
Ayrea HurleyDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, 77030, USA.
Annamaria CarissimoTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, NA, 80078, Italy.
Margherita MutarelliTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, NA, 80078, Italy.
Niya AleksievaMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, EH16 4UU, UK.ORCID http://orcid.org/0000-0002-7887-5494
Luca D'OrsiTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, NA, 80078, Italy.
William R LagorDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, 77030, USA.
David D MooreDepartment of Molecular and Cell Biology, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID http://orcid.org/0000-0002-5151-9748
Carmine SettembreTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, NA, 80078, Italy.
Milton J FinegoldDepartment of Pathology, Baylor College of Medicine, Houston, TX, 77030, USA.
Stuart J ForbesMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, EH16 4UU, UK.
Andrea BallabioJan and Dan Duncan Neurological Research Institute, Texas Children Hospital, Houston, TX, 77030, USA. ballabio@tigem.it.ORCID http://orcid.org/0000-0003-1381-4604
Baylor College of Medicine · USTelethon Institute Of Genetics And Medicine · ITMRC Centre for Regenerative Medicine · GBNeurological Research Institute · USFederico II University Hospital · IT

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MIRJANA MALETIC-SAVATIC · 2020 to 2026
$9.9M
Steps towards a paternal gene activation therapy for Angelman syndromeU54HD083092 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN, NEUL, JEFFREY L · 2014 to 2019
$7.8M
MODULATION OF CELLULAR CLEARANCE TO TREAT HUMAN DISEASER01NS078072 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI BALLABIO, ANDREA · 2012 to 2020
$3.1M
Tecan EVO GenePaint robotS10OD016167 · OD · BAYLOR COLLEGE OF MEDICINE · PI LJUNGBERG, CECILIA · 2013 to 2013
$215k
Medical Research Council MR/K017047/1Medical Research Council MR/R015635/1NCI NIH HHS P30 CA125123NICHD NIH HHS P50 HD103555NICHD NIH HHS U54 HD083092NIH HHS S10 OD016167NINDS NIH HHS R01 NS078072
6 · The paper itself

Abstract

It is well established that pluripotent stem cells in fetal and postnatal liver (LPCs) can differentiate into both hepatocytes and cholangiocytes. However, the signaling pathways implicated in the differentiation of LPCs are still incompletely understood. Transcription Factor EB (TFEB), a master regulator of lysosomal biogenesis and autophagy, is known to be involved in osteoblast and myeloid differentiation, but its role in lineage commitment in the liver has not been investigated. Here we show that during development and upon regeneration TFEB drives the differentiation status of murine LPCs into the progenitor/cholangiocyte lineage while inhibiting hepatocyte differentiation. Genetic interaction studies show that Sox9, a marker of precursor and biliary cells, is a direct transcriptional target of TFEB and a primary mediator of its effects on liver cell fate. In summary, our findings identify an unexplored pathway that controls liver cell lineage commitment and whose dysregulation may play a role in biliary cancer.

Indexed as

Cell LineageAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBile Duct NeoplasmsBile DuctsCell DifferentiationCell ProliferationCholangiocarcinomaDown-RegulationHepatocytesLiverMice, Inbred C57BLMice, TransgenicModels, BiologicalPhenotypePromoter Regions, GeneticBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsSOX9 Transcription FactorTcfeb protein, mouse

Identifiers

PMID32424153
PMCPMC7235048
OpenAlexW3025897174

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.