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Breast carcinomas with osteoclast-like giant cells: a comprehensive clinico-pathological and molecular portrait and evidence of RANK-L expression.
Cyrta, Joanna; Benoist, Camille; Masliah-Planchon, Julien; Vieira, Andre F; Pierron, Gaëlle; Fuhrmann, Laetitia; Richardot, Camille; Caly, Martial; Leclere, Renaud; Mariani, Odette; Da Maia, Elisabeth; Larousserie, Frédérique; Féron, Jean Guillaume; Carton, Matthieu; Renault, Victor; Bidard, François-Clément; Vincent-Salomon, Anne.
Affiliation
  • Cyrta J; Department of Pathology, Institut Curie, PSL Research University, Paris, France. joanna.cyrta@curie.fr.
  • Benoist C; Université de Paris, Paris, France. joanna.cyrta@curie.fr.
  • Masliah-Planchon J; Clinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.
  • Vieira AF; Somatic Genetics Unit, Institut Curie, Paris, France.
  • Pierron G; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Fuhrmann L; Somatic Genetics Unit, Institut Curie, Paris, France.
  • Richardot C; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Caly M; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Leclere R; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Mariani O; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Da Maia E; Platform of Experimental Pathology PATHEX, Institut Curie, Paris, France.
  • Larousserie F; Department of Pathology, Institut Curie, PSL Research University, Paris, France.
  • Féron JG; Department of Pathology, Hôpital de la Pitié-Salpêtrière, Paris, France.
  • Carton M; Department of Pathology, Hôpital Cochin, AP-HP, Université Paris Cité, Paris, France.
  • Renault V; Department of Surgery, Institut Curie, Paris, France.
  • Bidard FC; Department of Biometry, DRCI, Institut Curie, PSL Research University, Paris, France.
  • Vincent-Salomon A; Clinical Bioinformatics Unit, Institut Curie, PSL Research University, Paris, France.
Mod Pathol ; 35(11): 1624-1635, 2022 11.
Article in En | MEDLINE | ID: mdl-35697931
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Carcinoma / RANK Ligand Limits: Female / Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Breast Neoplasms / Carcinoma / RANK Ligand Limits: Female / Humans Language: En Year: 2022 Type: Article