Low progesterone receptor levels in high-grade DCIS correlate with HER2 upregulation and the presence of invasive components
- Hossein Schandiz 1,2, Lorant Farkas 2,3, Daehoon Park 3, Yan Liu 2,4, Solveig N Andersen 2, Jürgen Geisler 1,2, Torill Sauer 2
- Hossein Schandiz 1,2, Lorant Farkas 2,3, Daehoon Park 3
- 1Department of Oncology, Akershus University Hospital (AHUS), Lorenskog, Norway.
- 2Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
- 3Department of Pathology, Oslo University Hospital, Oslo, Norway.
- 4Department of Clinical Molecular Biology (EpiGen), Akershus University Hospital (AHUS), Lorenskog, Norway.
- 0Department of Oncology, Akershus University Hospital (AHUS), Lorenskog, Norway.
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View abstract on PubMed
Summary
This summary is machine-generated.This study analyzed molecular markers in high-grade breast ductal carcinoma in situ (DCIS), finding low progesterone receptor expression is linked to HER2 overexpression and invasive components in Luminal B subtypes.
Area Of Science
- Oncology
- Molecular Biology
- Pathology
Background
- High-grade breast ductal carcinoma in situ (DCIS) is a heterogeneous condition.
- Understanding molecular markers like estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth receptor 2 (HER2) is crucial for classifying DCIS subtypes.
Purpose Of The Study
- To investigate pivotal molecular markers (ER, PR, HER2) in human high-grade DCIS.
- To analyze these markers across different DCIS subtypes and their invasive potential.
Main Methods
- Classified 357 DCIS cases into subtypes (Luminal A, Luminal B HER2-, Luminal B HER2+, HER2-enriched, triple-negative) using 2013 St. Gallen guidelines.
- Categorized subtypes into "Pure" (no invasive component), "W/invasive" (with invasive component), and "All" groups.
- Assessed ER and PR expression intervals and HER2 status, using dual-color in situ hybridization for equivocal cases.
Main Results
- Over 90% of Luminal A cases showed ER and PR expression ≥ 50%.
- Significant differences in ER expression (<10% and ≥50%) were observed in Luminal A compared to other luminal subtypes (p < 0.0001).
- Low PR expression (<20%) in Luminal B subtypes was significantly associated with HER2 overexpression (3+) and invasive components (p = 0.0001 and p = 0.0365).
Conclusions
- High ER and PR expression is characteristic of Luminal A DCIS.
- Low PR expression in high-grade DCIS is a strong indicator of HER2 overexpression and the presence of an invasive component.
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