Evidence map›Paper›PMID 20616345›Full record

ReviewThe American journal of pathology2010

Role of Cripto-1 in stem cell maintenance and malignant progression.

Caterina Bianco, Maria Cristina Rangel, Nadia P Castro, Tadahiro Nagaoka, Kelly Rollman, Monica Gonzales, David S Salomon

Open access · bronzeAbstract readReview
In one paragraph

Review in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

67 citing papers in PubMed, 125 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Cripto Is Targeted by miR-1a-3p in a Mouse Model of Heart Development.International journal of molecular sciences · 2023
    Article
  10. Article
  11. Ablation of ZC3H11A causes early embryonic lethality and dysregulation of metabolic processes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Understanding the role of Cripto-1 in cancer progression and therapeutic strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  13. Article
  14. Article
  15. TGF-β superfamily co-receptors in cancer.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

7 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

Caterina BiancoMammary Biology and Tumorigenesis Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA. biancoc@mail.nih.gov
Maria Cristina Rangel
Nadia P Castro
Tadahiro Nagaoka
Kelly Rollman
Monica Gonzales
David S Salomon
National Institutes of Health · USCenter for Cancer Research · USNational Cancer Institute · US

Funding

The Role of Cripto in the Pathogenesis of Breast and Colon CancerZIABC009003 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SALOMON, DAVID · 2009 to 2016
$9.4M
Intramural NIH HHS
6 · The paper itself

Abstract

Cripto-1 is critical for early embryonic development and, together with its ligand Nodal, has been found to be associated with the undifferentiated status of mouse and human embryonic stem cells. Like other embryonic genes, Cripto-1 performs important roles in the formation and progression of several types of human tumors, stimulating cell proliferation, migration, epithelial to mesenchymal transition, and tumor angiogenesis. Several studies have demonstrated that cell fate regulation during embryonic development and cell transformation during oncogenesis share common signaling pathways, suggesting that uncontrolled activation of embryonic signaling pathways might drive cell transformation and tumor progression in adult tissues. Here we review our current understanding of how Cripto-1 controls stem cell biology and how it integrates with other major embryonic signaling pathways. Because many cancers are thought to derive from a subpopulation of cancer stem-like cells, which may re-express embryonic genes, Cripto-1 signaling may drive tumor growth through the generation or expansion of tumor initiating cells bearing stem-like characteristics. Therefore, the Cripto-1/Nodal signaling may represent an attractive target for treatment in cancer, leading to the elimination of undifferentiated stem-like tumor initiating cells.

Indexed as

Disease ProgressionAnimalsEmbryonic DevelopmentEpidermal Growth FactorEpithelial-Mesenchymal TransitionGPI-Linked ProteinsHumansHypoxiaIntercellular Signaling Peptides and ProteinsMembrane GlycoproteinsNeoplasm ProteinsNeoplasmsNeoplastic Stem CellsNodal ProteinReceptors, NotchSignal TransductionEpidermal Growth FactorGPI-Linked ProteinsIntercellular Signaling Peptides and ProteinsMembrane GlycoproteinsNeoplasm ProteinsNodal ProteinReceptors, NotchTDGF1 protein, humanWnt Proteins

Identifiers

PMID20616345
PMCPMC2913337
OpenAlexW2166361805

What OpenQuestion holds

Textmetadata
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.