Evidence map›Paper›PMID 26416446›Full record

ArticleOncotarget2015

Evaluation of a novel human IgG1 anti-claudin3 antibody that specifically recognizes its aberrantly localized antigen in ovarian cancer cells and that is suitable for selective drug delivery.

Chiara Romani, Emiliano Cocco, Eliana Bignotti, Daniele Moratto, Antonella Bugatti, Paola Todeschini, Elisabetta Bandiera, Renata Tassi, Laura Zanotti, Sergio Pecorelli and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Potential roles of claudin-3 and claudin-4 in ovarian cancer management.Journal of the Egyptian National Cancer Institute · 2022
    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

16 authors at 3 institutions in 3 countries.

Chiara Romani"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Emiliano CoccoDepartment of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Eliana Bignotti"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Daniele MorattoLaboratory of Genetic Disorders of Childhood, Angelo Nocivelli Institute for Molecular Medicine, Spedali Civili, Brescia, Italy.
Antonella BugattiDepartment of Pathology, University of Brescia, Brescia, Italy.
Paola Todeschini"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Elisabetta Bandiera"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Renata Tassi"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Laura Zanotti"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Sergio Pecorelli"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Enrico Sartori"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Franco E Odicino"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Ario de MarcoDepartment of Biomedical Science and Engineering, University of Nova Gorica, Vipava, Slovenia.
Alessandro Davide SantinDepartment of Molecular and Translational Medicine, Brescia, Italy.
Antonella Ravaggi"Angelo Nocivelli" Institute for Molecular Medicine, Division of Gynecologic Oncology, University of Brescia, Brescia, Italy.
Stefania MitolaDepartment of Pathology, University of Brescia, Brescia, Italy.
University of Brescia · ITUniversity of Nova Gorica · SIYale University · US

Funding

Integrated genomic analysis of racial disparities in endometrial cancerU01CA176067 · NCI · YALE UNIVERSITY · PI SANTIN, ALESSANDRO D · 2014 to 2018
$1.7M
CPE Peptide-Based Nanoparticles for the Diagnosis and Therapy of Chemotherapy ResR01CA154460 · NCI · YALE UNIVERSITY · PI SANTIN, ALESSANDRO D · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA154460NCI NIH HHS R01 CA154460-01NCI NIH HHS U01 CA176067NCI NIH HHS U01 CA176067-01A1
6 · The paper itself

Abstract

Membrane protein claudin3 has been recently suggested as a marker for biologically aggressive tumors and a possible target for the therapeutic delivery of active anti-cancer compounds. Claudin3-binding molecules such as the Clostridium perfringens enterotoxin (CPE), CPE-related molecules, and murine and chimeric antibodies have shown promising antitumor efficacy in preclinical oncological settings. We first engineered a fully human anti-claudin3 IgG1 antibody (IgGH6) by fusing the human IgG1 Fc-domain to the anti-claudin3 scFvH6 previously isolated from a pre-immune phage display library. The construct was expressed in mammalian cells and specifically targeted claudin3 endogenously expressed on the surface of different human ovarian cancer cell lines. No detectable cross-reactivity with other homologous claudins was observed. The epitope recognized by IgGH6 is located within the minor extracellular domain of claudin3 and becomes accessible only in tumor cells characterized by incomplete junction formation. Confocal microscopy experiments demonstrated that IgGH6 was actively internalized in tumor cells after binding to native claudin3 and co-localized, likely within intracellular vesicles, with the C-CPE peptide. Preliminary results indicate that IgGH6 accumulated in vivo in free claudin3 ovarian carcinoma xenografts. For its selective uptake in tumor cells and its human nature, IgGH6 represents a valuable candidate for antibody-drug conjugate therapeutic applications in ovarian cancer patients.

Indexed as

AnimalsAntibodies, NeoplasmAntibody AffinityAntineoplastic AgentsBlotting, WesternCell Line, TumorClaudin-3Drug CarriersDrug Delivery SystemsEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansImmunoglobulin GMiceMice, SCIDAntibodies, NeoplasmAntineoplastic AgentsClaudin-3CLDN3 protein, humanDrug CarriersImmunoglobulin GRNA, Small Interferingclaudinshuman antibodytherapeutic targettight junction

Identifiers

PMID26416446
PMCPMC4741477
OpenAlexW2268043966

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.