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Updated: Jun 15, 2025

Preparation of Tumor Antigen-loaded Mature Dendritic Cells for Immunotherapy
Published on: August 1, 2013
Bicalutamide reveals immunomodulatory effects in prostate cancer by regulating immunogenic dendritic cell maturation
Niloufar Sadat Nourbakhsh1, Sirous Naeimi2, Mehdi Moghanibashi3
1Department of Genetics, Faculty of Science, Kazerun Branch, Islamic Azad University, Kazerun, Iran.
Abstract:
Prostate cancer poses a significant global health challenge, ranking as the second most prevalent and fifth most lethal malignancy among males. The intricate interplay between androgen signaling and the immune microenvironment underscores the complexity of prostate cancer progression. Notably, androgen receptor (AR) signaling has been shown to affect immune response mediated by tumor antigen-presenting dendritic cells (DCs). Therefore, this study aimed to explore the potential of Bicalutamide, a nonsteroidal anti-androgen, in modulating DCs-mediated immune responses. Peripheral blood mononuclear cells (PBMCs) were isolated, and monocytes were extracted, followed by their differentiation into immature dendritic cells (iDCs) using GM-CSF and IL-4. Harvested tumor cell lysates from human prostate cancer cells were then utilized to induce the transformation of iDCs into mature dendritic cells (mDCs). Then, mDCs were treated with non-toxic concentration of Bicalutamide determined by annexin V/PI assay. The morphological characteristics of mDCs were investigated using an inverted light microscope. Flow cytometry was used to determine the cell surface expression of molecular markers of DC maturation, and qRT-PCR was employed to evaluate expression levels of proinflammatory genes involved in DC maturation. The obtained results indicated that Bicalutamide treatment of monocyte-derived mDCs induces an immunogenic and matured phenotype, marked by increased expression of CD86 and HLA-DR. Besides, qRT-PCR results evidenced that Bicalutamide decreased the expression of anti-inflammatory genes, including Interleukin-10 (IL-10) and TGF-beta, as an indication of immunogenic DCs. These findings suggest that beyond its established anti-androgen role, Bicalutamide may exert anti-tumor effects through the modulation of DCs-mediated immune responses. This novel immunomodulatory feature holds promise for the development of novel therapies, including combination therapies, in prostate cancer treatment.
Insights
Bicalutamide, an anti-androgen, promotes prostate cancer immune responses by maturing dendritic cells (DCs). This suggests Bicalutamide may offer new anti-tumor strategies beyond its known functions.
Area of Science:
- Oncology
- Immunology
Background:
- Prostate cancer is a major global health concern, with complex interactions between androgen signaling and the immune system.
- Androgen receptor (AR) signaling influences immune responses mediated by dendritic cells (DCs).
Purpose of the Study:
- To investigate Bicalutamide's potential to modulate DC-mediated immune responses in prostate cancer.
- To explore Bicalutamide's effects on dendritic cell maturation and immune signaling.
Main Methods:
- Monocytes were differentiated into immature dendritic cells (iDCs) and matured into mature dendritic cells (mDCs) using prostate cancer cell lysates.
- Mature DCs were treated with Bicalutamide, and its effects on cell surface markers (CD86, HLA-DR) and gene expression (IL-10, TGF-beta) were analyzed.
- Cell morphology and viability were assessed.
Main Results:
- Bicalutamide treatment induced a mature and immunogenic phenotype in monocyte-derived mDCs.
- Increased expression of CD86 and HLA-DR was observed on Bicalutamide-treated mDCs.
- Bicalutamide decreased the expression of anti-inflammatory genes (IL-10, TGF-beta).
Conclusions:
- Bicalutamide promotes an immunogenic mature dendritic cell phenotype.
- Beyond its anti-androgen effects, Bicalutamide may possess anti-tumor properties via immune modulation.
- These findings suggest Bicalutamide as a potential agent for novel prostate cancer therapies, including combination treatments.
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