Evidence map›Paper›PMID 26370966›Full record

ArticleInternational journal of molecular sciences2015

New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding.

Annalia Focà, Luca Sanguigno, Giuseppina Focà, Luigi Strizzi, Roberta Iannitti, Rosanna Palumbo, Mary J C Hendrix, Antonio Leonardi, Menotti Ruvo, Annamaria Sandomenico

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. 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
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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

10 authors at 5 institutions in 2 countries.

Annalia FocàInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. annalia.foca@gmail.com.
Luca SanguignoBioker Multimedica, Naples 80131, Italy. Luca.Sanguigno@multimedica.it.
Giuseppina FocàInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. giuseppina.foca@gmail.com.
Luigi StrizziProgram in Cancer Biology and Epigenomics, Stanley Manne Children's Research Institute at Ann and Robert H. Lurie Children's Hospital of Chicago, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. LStrizzi@luriechildrens.org.
Roberta IannittiInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. robertaiannitti@gmail.com.
Rosanna PalumboInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. rosanna.palumbo@cnr.it.
Mary J C HendrixProgram in Cancer Biology and Epigenomics, Stanley Manne Children's Research Institute at Ann and Robert H. Lurie Children's Hospital of Chicago, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. m-hendrix@northwestern.edu.
Antonio LeonardiDepartment of Molecular Medicine and Medical Biotechnologies, Università degli Studi di Napoli "Federico II", Naples 80131, Italy. leonardi@unina.it.
Menotti RuvoInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. menotti.ruvo@unina.it.
Annamaria SandomenicoInstitute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy. annamaria.sandomenico@gmail.com.
University of Naples Federico II · ITCentro Interuniversitario di Ricerca sui Peptidi Bioattivi · ITLurie Children's Hospital · USMultiMedica · ITNorthwestern University · US

Funding

Endothelial Transdifferentiation of Invasive Tumor CellsR37CA059702 · NCI · UNIVERSITY OF IOWA · PI HENDRIX, MARY J.C. · 2002 to 2011
$3.9M
Epigenetic Effect of the Microenvironment on Stem Cell Plasticity and FunctionR01CA121205 · NCI · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI HENDRIX, MARY J.C. · 2007 to 2011
$2.1M
NCI NIH HHS R01 CA121205NCI NIH HHS R01CA121205NCI NIH HHS R37 CA059702NCI NIH HHS R37CA59702
6 · The paper itself

Abstract

Nodal is a potent embryonic morphogen belonging to the TGF-β superfamily. Typically, it also binds to the ALK4/ActRIIB receptor complex in the presence of the co-receptor Cripto-1. Nodal expression is physiologically restricted to embryonic tissues and human embryonic stem cells, is absent in normal cells but re-emerges in several human cancers, including melanoma, breast, and colon cancer. Our aim was to obtain mAbs able to recognize Nodal on a major CBR (Cripto-Binding-Region) site and to block the Cripto-1-mediated signalling. To achieve this, antibodies were raised against hNodal(44-67) and mAbs generated by the hybridoma technology. We have selected one mAb, named 3D1, which strongly associates with full-length rhNodal (KD 1.4 nM) and recognizes the endogenous protein in a panel of human melanoma cell lines by western blot and FACS analyses. 3D1 inhibits the Nodal-Cripto-1 binding and blocks Smad2/3 phosphorylation. Data suggest that inhibition of the Nodal-Cripto-1 axis is a valid therapeutic approach against melanoma and 3D1 is a promising and interesting agent for blocking Nodal-Cripto mediated tumor development. These findings increase the interest for Nodal as both a diagnostic and prognostic marker and as a potential new target for therapeutic intervention.

Indexed as

Models, MolecularProtein Structure, SecondaryAmino Acid SequenceAntibodies, MonoclonalEpitope MappingEpitopesGPI-Linked ProteinsGrowth Differentiation FactorsHumansImmunoglobulin Fab FragmentsIntercellular Signaling Peptides and ProteinsMolecular Sequence DataNeoplasm ProteinsNodal ProteinPeptidesProtein BindingAntibodies, MonoclonalEpitopesGPI-Linked ProteinsGrowth Differentiation FactorsImmunoglobulin Fab FragmentsIntercellular Signaling Peptides and ProteinsNeoplasm ProteinsNodal ProteinPeptidesTDGF1 protein, humanFab fragmentsmelanomamonoclonal antibodynodalSPR

Identifiers

PMID26370966
PMCPMC4613256
OpenAlexW2098629747

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.