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


Journal

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
ISSN: 1530-0285
Titre abrégé: Mod Pathol
Pays: United States
ID NLM: 8806605

Informations de publication

Date de publication:
11 2022
Historique:
received: 02 04 2022
accepted: 12 05 2022
revised: 08 05 2022
pubmed: 14 6 2022
medline: 28 10 2022
entrez: 13 6 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 35697931
doi: 10.1038/s41379-022-01112-9
pii: S0893-3952(22)00229-0
pmc: PMC9596373
doi:

Substances chimiques

Iron E1UOL152H7
Macrophage Colony-Stimulating Factor 81627-83-0
Matrix Metalloproteinase 9 EC 3.4.24.35
Osteoprotegerin 0
Phosphatidylinositol 3-Kinases EC 2.7.1.-
Proto-Oncogene Proteins c-akt EC 2.7.11.1
TOR Serine-Threonine Kinases EC 2.7.11.1
RANK Ligand 0
TNFSF11 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1624-1635

Informations de copyright

© 2022. The Author(s).

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Auteurs

Joanna Cyrta (J)

Department of Pathology, Institut Curie, PSL Research University, Paris, France. joanna.cyrta@curie.fr.
Université de Paris, Paris, France. joanna.cyrta@curie.fr.

Camille Benoist (C)

Clinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.

Julien Masliah-Planchon (J)

Somatic Genetics Unit, Institut Curie, Paris, France.

Andre F Vieira (AF)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.

Gaëlle Pierron (G)

Somatic Genetics Unit, Institut Curie, Paris, France.

Laetitia Fuhrmann (L)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.

Camille Richardot (C)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.

Martial Caly (M)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.

Renaud Leclere (R)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.
Platform of Experimental Pathology PATHEX, Institut Curie, Paris, France.

Odette Mariani (O)

Department of Pathology, Institut Curie, PSL Research University, Paris, France.

Elisabeth Da Maia (E)

Department of Pathology, Hôpital de la Pitié-Salpêtrière, Paris, France.

Frédérique Larousserie (F)

Department of Pathology, Hôpital Cochin, AP-HP, Université Paris Cité, Paris, France.

Jean Guillaume Féron (JG)

Department of Surgery, Institut Curie, Paris, France.

Matthieu Carton (M)

Department of Biometry, DRCI, Institut Curie, PSL Research University, Paris, France.

Victor Renault (V)

Clinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.

François-Clément Bidard (FC)

Department of Medical Oncology, Institut Curie, UVSQ/Paris-Saclay University, St Cloud, France.

Anne Vincent-Salomon (A)

Department of Pathology, Institut Curie, PSL Research University, Paris, France. anne.salomon@curie.fr.

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