Evidence map›Paper›PMID 25205719›Full record

ArticleBiological chemistry2015

Cathepsin B-deficient mice as source of monoclonal anti-cathepsin B antibodies.

Ekkehard Weber, Elena Barbulescu, Rita Medek, Thomas Reinheckel, Mansoureh Sameni, Arulselvi Anbalagan, Kamiar Moin, Bonnie F Sloane

Abstract read
In one paragraph

Article in Biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. Article
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 2 countries.

Ekkehard Weber
Elena Barbulescu
Rita Medek
Thomas Reinheckel
Mansoureh Sameni
Arulselvi Anbalagan
Kamiar Moin
Bonnie F Sloane
Wayne State University · USMartin Luther University Halle-Wittenberg · DEUniversity of Freiburg · DE

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Proteolytic Pathways in Progression of Pre-Malignant Breast DiseaseR01CA131990 · NCI · WAYNE STATE UNIVERSITY · PI MATTINGLY, RAYMOND R, SLOANE, BONNIE F · 2008 to 2013
$1.9M
NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA131990
6 · The paper itself

Abstract

Cathepsin B has been demonstrated to be involved in several proteolytic processes that support tumor progression and metastasis and neurodegeneration. To further clarify its role, defined monoclonal antibodies are needed. As the primary structure of human cathepsin B is almost identical to that of the mouse, cathepsin B-deficient mice were used in a novel approach for generating such antibodies, providing the chance of an increased immune response to the antigen, human cathepsin B. Thirty clones were found to produce cathepsin B-specific antibodies. Seven of these antibodies were used to detect cathepsin B in MCF10-DCIS human breast cancer cells by immunocytochemistry and immunoblotting. Five different binding sites were identified by epitope mapping giving the opportunity to combine these antibodies in oligoclonal antibody mixtures for an improved detection of cathepsin B.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalCathepsin BCell Line, TumorElectrophoresis, Polyacrylamide GelEpitope MappingEpitopesFluorescent Antibody TechniqueHumansImmunoblottingMiceMolecular Sequence DataAntibodies, MonoclonalCathepsin BEpitopes

Identifiers

PMID25205719
PMCPMC4496956
OpenAlexW2312833931

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.