Evidence map›Paper›PMID 28945253›Full record

ArticleNature genetics2017

Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma.

Phillips Y Huang, Eve Kandyba, Arnaud Jabouille, Jonas Sjolund, Atul Kumar, Kyle Halliwill, Melissa McCreery, Reyno DelRosario, Hio Chung Kang, Christine E Wong and 6 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Lgr6Genes & diseases · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. All-International journal of molecular sciences · 2023
    Article
  14. Review
  15. Article
  16. The Immunogenetics of Acne.Advances in experimental medicine and biology · 2022
    Article
  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

16 authors at 5 institutions in 4 countries.

Phillips Y HuangHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.ORCID http://orcid.org/0000-0001-5807-1133
Eve KandybaHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Arnaud JabouilleHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Jonas SjolundDivision of Translational Cancer Research, University of Lund, Lund, Sweden.ORCID http://orcid.org/0000-0002-6992-3415
Atul KumarHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Kyle HalliwillHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Melissa McCreeryHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Reyno DelRosarioHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.
Hio Chung KangInvitae Corp, San Francisco, California, USA.
Christine E WongInstitute of Cell Biology, ETH, Zurich, Switzerland.
Jost SeiblerTaconic Biosciences GmbH, Cologne, Germany.
Vincent BeugerTaconic Biosciences GmbH, Cologne, Germany.
Maurizio PellegrinoMission Bio, Inc., San Francisco, California, USA.
Adam SciambiMission Bio, Inc., San Francisco, California, USA.
Dennis J EastburnMission Bio, Inc., San Francisco, California, USA.
Allan BalmainHelen Diller Family Comprehensive Cancer Center University of California, San Francisco, San Francisco, California, USA.ORCID http://orcid.org/0000-0001-6549-7861
University of California, San Francisco · USMission Bio (United States) · USETH Zurich · CHInvitae (United States) · USLund University · SE

Funding

Identification of epithelial tumor susceptiility genesU01CA084244 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BALMAIN, ALLAN · 1999 to 2013
$13.3M
PREDOCTORAL TRAINING IN BIOMEDICAL SCIENCEST32GM008568 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANSEL, KARL MARK · 1995 to 2019
$6.3M
Science Leadership and IntegrationU01CA141455 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BALMAIN, ALLAN · 2009 to 2013
$3.2M
Genetic network analysis of cancer targetsU01CA176287 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WEISS, WILLIAM A · 2013 to 2016
$1.2M
High-throughput single-cell sorting and sequencing with PACSR44HG007814 · NHGRI · MISSION BIO, INC. · PI EASTBURN, DENNIS J · 2015 to 2016
$1.1M
Genetic analysis of ras mutation specificity in skin and lung cancerR01CA184510 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BALMAIN, ALLAN · 2015 to 2017
$1.1M
NCI NIH HHS R01 CA184510NCI NIH HHS U01 CA084244NCI NIH HHS U01 CA141455NCI NIH HHS U01 CA176287NHGRI NIH HHS R44 HG007814NIGMS NIH HHS T32 GM008568
6 · The paper itself

Abstract

The G-protein-coupled receptors LGR4, LGR5 and LGR6 are Wnt signaling mediators, but their functions in squamous cell carcinoma (SCC) are unclear. Using lineage tracing in Lgr5-EGFP-CreERT2/Rosa26-Tomato and Lgr6-EGFP-CreERT2/Rosa26-Tomato reporter mice, we demonstrate that Lgr6, but not Lgr5, acts as an epithelial stem cell marker in SCCs in vivo. We identify, by single-molecule in situ hybridization and cell sorting, rare cells positive for Lgr6 expression in immortalized keratinocytes and show that their frequency increases in advanced SCCs. Lgr6 expression is enriched in cells with stem cell characteristics, and Lgr6 downregulation in vivo causes increased epidermal proliferation with expanded lineage tracing from epidermal stem cells positive for Lgr6 expression. Surprisingly, mice with germline knockout of Lgr6 are predisposed to SCC development, through a mechanism that includes compensatory upregulation of Lgr5. These data provide a model for human patients with germline loss-of-function mutations in Wnt pathway genes, including RSPO1 or LGR4, who show increased susceptibility to squamous tumor development.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinoma, Squamous CellCell Line, TransformedEpidermisHumansKeratinocytesMiceMice, TransgenicNeoplastic Stem CellsReceptors, G-Protein-CoupledRNA, Small InterferingSignal TransductionSkin NeoplasmsThrombospondinsLGR4 protein, mouseLgr5 protein, mouseLgr6 protein, mouseReceptors, G-Protein-CoupledRNA, Small InterferingRSPO1 protein, mouseThrombospondins

Identifiers

PMID28945253
PMCPMC5662105
OpenAlexW2756747062

What OpenQuestion holds

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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.