Evidence map›Paper›PMID 35697931›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2022

Breast carcinomas with osteoclast-like giant cells: a comprehensive clinico-pathological and molecular portrait and evidence of RANK-L expression.

Joanna Cyrta, Camille Benoist, Julien Masliah-Planchon, Andre F Vieira, Gaëlle Pierron, Laetitia Fuhrmann, Camille Richardot, Martial Caly, Renaud Leclere, Odette Mariani and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

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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

17 authors at 5 institutions in 1 country.

Joanna CyrtaDepartment of Pathology, Institut Curie, PSL Research University, Paris, France. joanna.cyrta@curie.fr.ORCID 0000-0002-0216-5330
Camille BenoistClinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.
Julien Masliah-PlanchonSomatic Genetics Unit, Institut Curie, Paris, France.
Andre F VieiraDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.
Gaëlle PierronSomatic Genetics Unit, Institut Curie, Paris, France.
Laetitia FuhrmannDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0003-1755-6307
Camille RichardotDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.
Martial CalyDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.
Renaud LeclereDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.
Odette MarianiDepartment of Pathology, Institut Curie, PSL Research University, Paris, France.
Elisabeth Da MaiaDepartment of Pathology, Hôpital de la Pitié-Salpêtrière, Paris, France.
Frédérique LarousserieDepartment of Pathology, Hôpital Cochin, AP-HP, Université Paris Cité, Paris, France.
Jean Guillaume FéronDepartment of Surgery, Institut Curie, Paris, France.
Matthieu CartonDepartment of Biometry, DRCI, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0002-6793-3273
Victor RenaultClinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.
François-Clément BidardDepartment of Medical Oncology, Institut Curie, UVSQ/Paris-Saclay University, St Cloud, France.ORCID 0000-0001-5932-8949
Anne Vincent-SalomonDepartment of Pathology, Institut Curie, PSL Research University, Paris, France. anne.salomon@curie.fr.ORCID 0000-0001-5754-5771
Université Paris Sciences et Lettres · FRInstitut Curie · FRUniversité Paris Cité · FRSorbonne Université · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast carcinomas (BC) with osteoclast-like giant cells (OGC) are rare. Despite their distinct stromal features, their molecular characteristics remain unknown. Here, we report comprehensive clinico-pathological and molecular findings for 27 patients diagnosed with BC-OGC at Institut Curie between 2000 and 2021. Seventeen (63%) cases were invasive carcinomas of no special type (IC NST) with OGC (OGC-IC NST), four (15%) were mixed or multifocal cases with and without OGC (OGC-Mixed), and six (22%) were metaplastic carcinomas with OGC (OGC-MC). All OGC-IC NST and OGC-Mixed cases were ER+ HER2- tumors (most being luminal A based on transcriptomic subtyping, when available), while all OGC-MC were triple-negative. The median age at diagnosis was 46, 45 and 62 years for OGC-IC NST, OGC-Mixed and OGC-MC, respectively. Three patients developed distant metastases (one OGC-IC NST, two OGC-Mixed), one of whom died of metastatic disease (OGC-Mixed), and one other patient died of locally advanced disease (OGC-MC). Histopathological evaluation comparing 13 OGC-IC NST and 19 control IC NST without OGC confirmed that OGC-IC NST showed significantly higher density of vessels (by CD34 immunohistochemistry (IHC)), iron deposits (Perls stain), and CD68 and CD163-positive cell infiltrates. Genomic findings for nine OGC-IC NST and four OGC-MC were consistent with the underlying histologic subtype, including activating alterations of the PI3K/AKT/mTOR pathway in 7/13 cases. Using RNA-seq data, differential gene expression analysis between OGC-IC NST (n = 7) and control IC NST without OGC (n = 7) revealed significant overexpression of TNFSF11 (RANK-L), TNFRSF11A (RANK), CSF1 (M-CSF), CSF1R, and genes encoding osteoclastic enzymes (MMP9, ACP5, CTSK, CTSB) in OGC-IC NST, while OPG (osteoprotegerin) was underexpressed. We also confirmed for the first time RANK-L expression in BC with OGC by IHC (seen in 15 out of 16 cases, and only in 2 of 16 controls without OGC). These findings could offer a rationale for further investigating RANK-L as a therapeutic target in BC with OGC.

Indexed as

Breast NeoplasmsCarcinomaRANK LigandFemaleGiant CellsHumansIronMacrophage Colony-Stimulating FactorMatrix Metalloproteinase 9OsteoclastsOsteoprotegerinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesIronMacrophage Colony-Stimulating FactorMatrix Metalloproteinase 9OsteoprotegerinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRANK LigandTNFSF11 protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID35697931
PMCPMC9596373
OpenAlexW4282584386

What OpenQuestion holds

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LicenceCC BY
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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.