Evidence map›Paper›PMID 30912742›Full record

ArticleeLife2019

Homeostatic and tumourigenic activity of SOX2+ pituitary stem cells is controlled by the LATS/YAP/TAZ cascade.

Emily J Lodge, Alice Santambrogio, John P Russell, Paraskevi Xekouki, Thomas S Jacques, Randy L Johnson, Selvam Thavaraj, Stefan R Bornstein, Cynthia Lilian Andoniadou

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Pituitary Tumorigenesis-Implications for Management.Medicina (Kaunas, Lithuania) · 2023
    Review
  10. Review
  11. Review
  12. Cellular interactions in the pituitary stem cell niche.Cellular and molecular life sciences : CMLS · 2022
    Review
  13. Article
  14. Article
  15. Interleukin-6 is an activator of pituitary stem cells upon local damage, a competence quenched in the aging gland.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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 3 countries.

Emily J LodgeCentre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.ORCID 0000-0003-0932-8515
Alice SantambrogioCentre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
John P RussellCentre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
Paraskevi XekoukiCentre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
Thomas S JacquesUCL GOS Institute of Child Health and Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Randy L JohnsonDepartment of Cancer Biology, The University of Texas, MD Anderson Cancer Center, Houston, United States.
Selvam ThavarajCentre for Oral, Clinical and Translational Sciences, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
Stefan R BornsteinDivision of Diabetes & Nutritional Sciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.
Cynthia Lilian AndoniadouCentre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.ORCID 0000-0003-4311-5855
King's College London · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBThe University of Texas MD Anderson Cancer Center · US

Funding

Deutsche Forschungsgemeinschaft CRC/Transregio 205/1Deutsche Forschungsgemeinschaft GRK 2251Guy's and St Thomas' Charity Prize PhD ProgrammeKing's College London Dianna Trebble Endowment Fund Dental Institute StudentshipLister Institute of Preventive Medicine Prize Fellowship 2016Medical Research Council MR/L016729/1
6 · The paper itself

Abstract

SOX2 positive pituitary stem cells (PSCs) are specified embryonically and persist throughout life, giving rise to all pituitary endocrine lineages. We have previously shown the activation of the STK/LATS/YAP/TAZ signalling cascade in the developing and postnatal mammalian pituitary. Here, we investigate the function of this pathway during pituitary development and in the regulation of the SOX2 cell compartment. Through loss- and gain-of-function genetic approaches, we reveal that restricting YAP/TAZ activation during development is essential for normal organ size and specification from SOX2+ PSCs. Postnatal deletion of LATS kinases and subsequent upregulation of YAP/TAZ leads to uncontrolled clonal expansion of the SOX2+ PSCs and disruption of their differentiation, causing the formation of non-secreting, aggressive pituitary tumours. In contrast, sustained expression of YAP alone results in expansion of SOX2+ PSCs capable of differentiation and devoid of tumourigenic potential. Our findings identify the LATS/YAP/TAZ signalling cascade as an essential component of PSC regulation in normal pituitary physiology and tumourigenesis.

Indexed as

Cell ProliferationSignal TransductionAdaptor Proteins, Signal TransducingAnimalsCell Cycle ProteinsGene DeletionGene Regulatory NetworksMicePituitary GlandProtein Serine-Threonine KinasesSOXB1 Transcription FactorsStem CellsTrans-ActivatorsTumor Suppressor ProteinsYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingCell Cycle ProteinsLats1 protein, mouseLATS2 protein, mouseProtein Serine-Threonine KinasesSox2 protein, mouseSOXB1 Transcription FactorsTrans-ActivatorsTumor Suppressor ProteinsWwtr1 protein, mouseYap1 protein, mouseYAP-Signaling ProteinsHippoLATSmousepituitary stem cellpituitary tumourregenerative medicineSOX2stem cellsYAP

Identifiers

PMID30912742
PMCPMC6461440
OpenAlexW2903836972

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.