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Updated: Jun 23, 2025

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Folate Receptor Alpha Expression and the Tumor Immune Microenvironment in Patients with Cervical Cancer.
Shu Yazaki1, Yohei Chiba1, Yuki Kojima1
1Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Folate receptor alpha (FRα) is more common in cervical cancer patients with low PD-L1 expression. Targeting FRα may benefit patients with low or negative PD-L1 status, suggesting a new therapeutic strategy.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Folate receptor alpha (FRα) is a cell-surface protein and a potential cancer treatment target.
- Understanding FRα's role in the tumor immune microenvironment is crucial for cervical cancer therapy.
Purpose of the Study:
- To investigate the association between FRα expression and the tumor immune microenvironment in cervical cancer patients.
- To explore the correlation between FRα, PD-L1 expression, and patient prognosis.
Main Methods:
- Examined 123 cervical cancer tumor sections (squamous cell carcinoma and non-SCC).
- Assessed FRα expression via immunohistochemistry (clone 26B3).
- Evaluated PD-L1 expression (Combined Positive Score - CPS), CD3, and CD8 cell densities.
Main Results:
- FRα positivity was found in 72.4% of patients, varying by histology (55.2% SCC vs. 92.9% non-SCC).
- PD-L1 positivity (CPS ≥1) was observed in 75.6%, more frequent in SCC (83.5% vs. 66.1%).
- FRα expression showed weak negative correlations with PD-L1 (r=-0.22) and CD8+ cells (r=-0.19). FRα-high correlated with poor prognosis, especially in PD-L1 CPS ≥10 groups (HR: 4.10).
Conclusions:
- FRα expression is higher in cervical cancer patients with PD-L1 CPS <10 compared to those with CPS ≥10.
- Targeting FRα may represent a viable therapeutic strategy for cervical cancer patients with low or negative PD-L1 expression.
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