Evidence map›Paper›PMID 28813673›Full record

ArticleCell reports2017

Multipotent Basal Stem Cells, Maintained in Localized Proximal Niches, Support Directed Long-Ranging Epithelial Flows in Human Prostates.

Mohammad Moad, Edouard Hannezo, Simon J Buczacki, Laura Wilson, Amira El-Sherif, David Sims, Robert Pickard, Nicholas A Wright, Stuart C Williamson, Doug M Turnbull and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Dual Role of DLK1 in GnRH Neuron Ontogeny.Stem cell reviews and reports · 2025
    Article
  6. The role of estrogen receptor β in maintaining basal cells and modulating the immune environment in the prostate.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Cancer Stem Cells and Prostate Cancer: A Narrative Review.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Review
  15. Lineage tracing in human tissues.The Journal of pathology · 2022
    Review
  16. Review
  17. Prostate organogenesis.Development (Cambridge, England) · 2022
    Article
  18. Article
  19. Review
  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

15 authors at 10 institutions in 2 countries.

Mohammad MoadNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne NE2 4AD, UK.
Edouard HannezoCavendish Laboratory, Department of Physics, University of Cambridge, J.J. Thomson Avenue, Cambridge CB3 0HE, UK; Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Simon J BuczackiCancer Research UK, Cambridge Institute, University of Cambridge, Cambridge CB2 0RE, UK.
Laura WilsonNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne NE2 4AD, UK.
Amira El-SherifDepartment of Histopathology, Royal Victoria Infirmary, Newcastle upon Tyne NE1 4LP, UK; Department of Pathology, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
David SimsComputational Genomics Analysis and Training (CGAT), MRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK.
Robert PickardInstitute of Cellular Medicine, Medical School, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Nicholas A WrightBarts Cancer Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UK.
Stuart C WilliamsonClinical and Experimental Pharmacology Group, University of Manchester, Manchester M13 9PL, UK.
Doug M TurnbullWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; Newcastle Centre for Ageing and Vitality, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Robert W TaylorWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Laura GreavesWellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; Newcastle Centre for Ageing and Vitality, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Craig N RobsonNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne NE2 4AD, UK.
Benjamin D SimonsCavendish Laboratory, Department of Physics, University of Cambridge, J.J. Thomson Avenue, Cambridge CB3 0HE, UK; Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Wellcome Trust/Medical Research Council Stem Cell Institute, Cambridge CB2 1QR, UK. Electronic address: bds10@cam.ac.uk.
Rakesh HeerNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne NE2 4AD, UK. Electronic address: rakesh.heer@ncl.ac.uk.
Newcastle University · GBGenomics (United Kingdom) · GBNewcastle Hospitals - Campus for Ageing and Vitality · GBQueen Mary University of London · GBRoyal Victoria Infirmary · GBUniversity of Cambridge · GBUniversity of Manchester · GBWellcome/Cancer Research UK Gurdon Institute · GBWellcome Centre for Mitochondrial Research · GBWellcome Trust · GB

Funding

Biotechnology and Biological Sciences Research CouncilCancer Research Institute C10169/A12173Cancer Research UK 12173Cancer Research UK 14895Cancer Research UK 16485Medical Research Council G0601943Medical Research Council G0700718Medical Research Council MC_PC_12009Medical Research Council MC_PC_15065Medical Research Council MR/L016354/1Wellcome TrustWellcome Trust 096919/Z/11/ZWellcome Trust 098357/Z/12/ZWellcome Trust 110326/Z/15/Z
6 · The paper itself

Abstract

Sporadic mitochondrial DNA mutations serve as clonal marks providing access to the identity and lineage potential of stem cells within human tissues. By combining quantitative clonal mapping with 3D reconstruction of adult human prostates, we show that multipotent basal stem cells, confined to discrete niches in juxta-urethral ducts, generate bipotent basal progenitors in directed epithelial migration streams. Basal progenitors are then dispersed throughout the entire glandular network, dividing and differentiating to replenish the loss of apoptotic luminal cells. Rare lineage-restricted luminal stem cells, and their progeny, are confined to proximal ducts and provide only minor contribution to epithelial homeostasis. In situ cell capture from clonal maps identified delta homolog 1 (DLK1) enrichment of basal stem cells, which was validated in functional spheroid assays. This study establishes significant insights into niche organization and function of prostate stem and progenitor cells, with implications for disease.

Indexed as

BiomarkersCalcium-Binding ProteinsCell DifferentiationCell LineageDNA, MitochondrialEpithelial CellsGene ExpressionHumansIntercellular Signaling Peptides and ProteinsLaser Capture MicrodissectionMaleMembrane ProteinsMultipotent Stem CellsPrimary Cell CultureProstateRNABiomarkersCalcium-Binding ProteinsDLK1 protein, humanDNA, MitochondrialIntercellular Signaling Peptides and ProteinsMembrane ProteinsRNAbasalbranchDLK1epitheliumluminalnicheNotchorganoidsprostateprostate cancerstem cell

Identifiers

PMID28813673
PMCPMC5565638
OpenAlexW2746340372

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.