Evidence map›Paper›PMID 25153355›Full record

ReviewSeminars in cancer biology2014

The multifaceted role of the embryonic gene Cripto-1 in cancer, stem cells and epithelial-mesenchymal transition.

Malgorzata Klauzinska, Nadia P Castro, Maria Cristina Rangel, Benjamin T Spike, Peter C Gray, Daniel Bertolette, Frank Cuttitta, David Salomon

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.3field-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

69 citing papers in PubMed, 104 citations in OpenAlex.

  1. Trial
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  5. Genomic evolution of EGF-CFC genes in deuterostomes.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
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9 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

8 authors at 3 institutions in 1 country.

Malgorzata KlauzinskaMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA.
Nadia P CastroMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA.
Maria Cristina RangelMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA.
Benjamin T SpikeGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Peter C GrayClayton Foundation Laboratories for Peptide Biology, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Daniel BertoletteMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA.
Frank CuttittaMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA.
David SalomonMouse Cancer Genetics Program, Center for Cancer Research, Frederick, MD 21702, USA. Electronic address: salomond@mail.nih.gov.
Cancer Genetics (United States) · USCenter for Cancer Research · USSalk Institute for Biological Studies · 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
THE ROLE OF EGF-RELATED PEPTIDES IN THE PATHOGENESIS OF BREAST AND COLON CANCERZ01BC009003 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SALOMON, DAVID · 1996 to 2008
$2.4M
Intramural NIH HHS Z01 BC009003
6 · The paper itself

Abstract

Cripto-1 (CR-1)/Teratocarcinoma-derived growth factor1 (TDGF-1) is a cell surface glycosylphosphatidylinositol (GPI)-linked glycoprotein that can function either in cis (autocrine) or in trans (paracrine). The cell membrane cis form is found in lipid rafts and endosomes while the trans acting form lacking the GPI anchor is soluble. As a member of the epidermal growth factor (EGF)/Cripto-1-FRL-1-Cryptic (CFC) family, CR-1 functions as an obligatory co-receptor for the transforming growth factor-β (TGF-β) family members, Nodal and growth and differentiation factors 1 and 3 (GDF1/3) by activating Alk4/Alk7 signaling pathways that involve Smads 2, 3 and 4. In addition, CR-1 can activate non-Smad-dependent signaling elements such as PI3K, Akt and MAPK. Both of these pathways depend upon the 78kDa glucose regulated protein (GRP78). Finally, CR-1 can facilitate signaling through the canonical Wnt/β-catenin and Notch/Cbf-1 pathways by functioning as a chaperone protein for LRP5/6 and Notch, respectively. CR-1 is essential for early embryonic development and maintains embryonic stem cell pluripotentiality. CR-1 performs an essential role in the etiology and progression of several types of human tumors where it is expressed in a population of cancer stem cells (CSCs) and facilitates epithelial-mesenchymal transition (EMT). In this context, CR-1 can significantly enhance tumor cell migration, invasion and angiogenesis. Collectively, these facts suggest that CR-1 may be an attractive target in the diagnosis, prognosis and therapy of several types of human cancer.

Indexed as

Activin Receptors, Type Ibeta CateninCell MembraneEndoplasmic Reticulum Chaperone BiPEpithelial-Mesenchymal TransitionGPI-Linked ProteinsHeat-Shock ProteinsHumansIntercellular Signaling Peptides and ProteinsMembrane ProteinsNeoplasm InvasivenessNeoplasm ProteinsNeoplasmsNeoplastic Stem CellsNeovascularization, PathologicPhosphatidylinositol 3-KinasesActivin Receptors, Type IACVR1B protein, humanACVR1C protein, humanbeta CateninEndoplasmic Reticulum Chaperone BiPGPI-Linked ProteinsHeat-Shock ProteinsHSPA5 protein, humanHspa5 protein, mouseIntercellular Signaling Peptides and ProteinsMembrane ProteinsNeoplasm ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, NotchSmad2 ProteinSMAD2 protein, humanSmad3 ProteinSmad4 ProteinTDGF1 protein, humanTGF-beta Superfamily ProteinsTransforming Growth Factor betaWnt ProteinsCancerCripto-1Epithelial-mesenchymal transitionGRP78Stem cells

Identifiers

PMID25153355
PMCPMC4252566
OpenAlexW2049273387

What OpenQuestion holds

Textmetadata
LicenceTDM
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.