Evidence map›Paper›PMID 29085663›Full record

ArticleThe journal of pathology. Clinical research2017

Isoform specificity of progesterone receptor antibodies.

Victoria Fabris, María F Abascal, Sebastián Giulianelli, María May, Gonzalo R Sequeira, Britta Jacobsen, Marc Lombès, Julie Han, Luan Tran, Alfredo Molinolo and 1 more

Open access · goldAbstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. A molecular toolbox to study progesterone receptor signaling.Journal of mammary gland biology and neoplasia · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Progesterone and Breast Cancer.Endocrine reviews · 2020
    Review
  8. Article
  9. 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

11 authors at 4 institutions in 3 countries.

Victoria FabrisLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.
María F AbascalLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.
Sebastián GiulianelliLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.
María MayLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.
Gonzalo R SequeiraLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.
Britta JacobsenUniversity of Colorado Anschutz Medical CampusAuroraCOUSA.
Marc LombèsUnité Mixte de Recherche, INSERM U 1185, Fac Med Paris SudUniversité Paris SaclayFrance.
Julie HanDepartment of Pathology, Moore's Cancer Center, UCSDLa JollaCAUSA.
Luan TranDepartment of Pathology, Moore's Cancer Center, UCSDLa JollaCAUSA.
Alfredo MolinoloDepartment of Pathology, Moore's Cancer Center, UCSDLa JollaCAUSA.
Claudia LanariLaboratorio de Carcinogénesis Hormonal, Instituto de Biología y Medicina Experimental (IBYME), CONICETBuenos AiresArgentina.ORCID 0000-0003-0555-2309
Consejo Nacional de Investigaciones Científicas y Técnicas · ARNational Foundation for Cancer Research · USUniversité Paris-Sud · FRUniversity of Colorado Anschutz Medical Campus · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone-dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N-terminal amino acids. It has been reported that several antibodies empirically exclusively recognize PRA in formalin-fixed paraffin-embedded (FFPE) tissues. To confirm these findings, we used human breast cancer xenograft models, T47D-YA and -YB cells expressing PRA or PRB, respectively, MDA-MB-231 cells modified to synthesize PRB, and MDA-MB-231/iPRAB cells which can bi-inducibly express either PRA or PRB. Cells were injected into immunocompromised mice to generate tumours exclusively expressing PRA or PRB. PR isoform expression was verified using immunoblots. FFPE samples from the same tumours were studied by immunohistochemistry using H-190, clone 636, clone 16, and Ab-6 anti-PR antibodies, the latter exclusively recognizing PRB. Except for Ab-6, all antibodies displayed a similar staining pattern. Our results indicate that clones 16, 636, and the H-190 antibody recognize both PR isoforms. They point to the need for more stringency in evaluating the true specificity of purported PRA-specific antibodies as the PRA/PRB ratio may have prognostic and predictive value in breast cancer.

Indexed as

breast cancer modelsimmunohistochemistryprogesterone receptor isoformsspecific antibodiesxenografts

Identifiers

PMID29085663
PMCPMC5653926
OpenAlexW2754520699

What OpenQuestion holds

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LicenceCC BY-NC
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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.