Evidence map›Paper›PMID 24749068›Full record

ArticleStem cell reports2014

CRIPTO/GRP78 signaling maintains fetal and adult mammary stem cells ex vivo.

Benjamin T Spike, Jonathan A Kelber, Evan Booker, Madhuri Kalathur, Rose Rodewald, Julia Lipianskaya, Justin La, Marielle He, Tracy Wright, Richard Klemke and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. CRIPTO antagonist ALK4Breast cancer research : BCR · 2020
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Cripto stabilizes GRP78 on the cell membrane.Protein science : a publication of the Protein Society · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. GRP78 haploinsufficiency suppresses acinar-to-ductal metaplasia, signaling, and mutantProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. 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

12 authors at 2 institutions in 1 country.

Benjamin T SpikeGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Jonathan A KelberDepartment of Pathology, University of California, San Diego, La Jolla, CA 92037, USA.
Evan BookerClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Madhuri KalathurClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Rose RodewaldGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Julia LipianskayaGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Justin LaGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Marielle HeClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Tracy WrightDepartment of Pathology, University of California, San Diego, La Jolla, CA 92037, USA.
Richard KlemkeDepartment of Pathology, University of California, San Diego, La Jolla, CA 92037, USA.
Geoffrey M WahlGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Peter C GrayClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Salk Institute for Biological Studies · USUniversity of California, San Diego · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Vascular communication in metastatic brain colonizationR01CA184594 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KLEMKE, RICHARD L. · 2014 to 2018
$1.6M
NCI NIH HHS P30 CA014195NCI NIH HHS R01 CA184594
6 · The paper itself

Abstract

Little is known about the extracellular signaling factors that govern mammary stem cell behavior. Here, we identify CRIPTO and its cell-surface receptor GRP78 as regulators of stem cell behavior in isolated fetal and adult mammary epithelial cells. We develop a CRIPTO antagonist that promotes differentiation and reduces self-renewal of mammary stem cell-enriched populations cultured ex vivo. By contrast, CRIPTO treatment maintains the stem cell phenotype in these cultures and yields colonies with enhanced mammary gland reconstitution capacity. Surface expression of GRP78 marks CRIPTO-responsive, stem cell-enriched fetal and adult mammary epithelial cells, and deletion of GRP78 from adult mammary epithelial cells blocks their mammary gland reconstitution potential. Together, these findings identify the CRIPTO/GRP78 pathway as a developmentally conserved regulator of fetal and adult mammary stem cell behavior ex vivo, with implications for the stem-like cells found in many cancers.

Indexed as

Signal TransductionActivin Receptors, Type IAdult Stem CellsBiomarkersCell DifferentiationCell LineCell MembraneCells, CulturedEndoplasmic Reticulum Chaperone BiPEpithelial CellsGene ExpressionGPI-Linked ProteinsHeat-Shock ProteinsHumansIntercellular Signaling Peptides and ProteinsMammary Glands, HumanActivin Receptors, Type IACVR1B protein, humanBiomarkersEndoplasmic Reticulum Chaperone BiPGPI-Linked ProteinsHeat-Shock ProteinsHSPA5 protein, humanIntercellular Signaling Peptides and ProteinsNeoplasm ProteinsTDGF1 protein, human

Identifiers

PMID24749068
PMCPMC3986630
OpenAlexW1989075744

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.