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Updated: Mar 24, 2026

Isolation, Culture, and Characterization of Prostate Cancer-Associated Fibroblasts
Published on: August 1, 2025
Nanomedicine Targeting Cancer-Associated Fibroblasts in Prostate Cancer: From Biological Mechanisms to Integrated
Fajiang Qian1, Jingfeng Zhou2, Yuan Tang3
1Department of Urology, Lincang People's Hospital, Lincang, Yunnan, 677000, People's Republic of China.
Abstract:
Prostate cancer (PCa) is the second most common malignancy in men worldwide. Advanced stages are characterized by tumor heterogeneity, metastasis, and resistance to androgen deprivation therapy and chemotherapy. Cancer-associated fibroblasts (CAFs), the predominant stromal cells in the PCa tumor microenvironment (TME), critically drive tumor progression, metastasis, and therapeutic resistance. Nanomedicine represents a transformative strategy for targeting CAFs. It leverages engineered nanomaterials to achieve precise drug delivery, improved bioavailability, and multimodal theranostic capabilities, which integrate diagnosis with therapy. This review comprehensively examines advances in nanomaterial-based strategies for CAF-targeted therapy in PCa. We first delineate the biology of CAFs in PCa, encompassing their origins, activation mechanisms, key markers (e.g, α-SMA and FAP), phenotypic heterogeneity, and intricate crosstalk with cancer cells, immune cells, and the extracellular matrix (ECM). We then evaluate nanomaterial-based targeting strategies and therapeutic modalities, including CAF depletion, reprogramming, and extracellular matrix remodeling, for the treatment of PCa. Subsequently, we discuss CAF-targeted nanoplatforms for theranostics, including molecular imaging probes (e.g., 68Ga-FAPI) and image-guided delivery systems that integrate precise diagnosis with therapy. Finally, we address key challenges, particularly CAF heterogeneity and nanomaterial biosafety, and outline future directions, including gene-editing integration, multi-stimuli-responsive systems, and synergistic immunotherapy combinations. Collectively, this review underscores the transformative potential of integrating CAF biology with nanotechnology to overcome therapeutic resistance in PCa and advance precision oncology.
Insights
Nanomedicine offers a promising approach to target cancer-associated fibroblasts (CAFs) in prostate cancer (PCa). This strategy aims to overcome therapeutic resistance by leveraging nanomaterials for precise delivery and theranostics.
Area of Science:
- Oncology
- Nanotechnology
- Cancer Biology
Background:
- Prostate cancer (PCa) is a leading malignancy in men, often developing resistance to standard therapies.
- Cancer-associated fibroblasts (CAFs) within the tumor microenvironment (TME) significantly contribute to PCa progression, metastasis, and treatment resistance.
Purpose of the Study:
- To review advancements in nanomaterial-based strategies for targeting CAFs in PCa.
- To explore the integration of nanomedicine with CAF biology for improved PCa treatment and theranostics.
Main Methods:
- Comprehensive review of literature on CAF biology in PCa.
- Evaluation of nanomaterial-based targeting strategies (depletion, reprogramming, ECM remodeling).
- Discussion of nanoplatforms for CAF-targeted theranostics and imaging (e.g., 68Ga-FAPI).
Main Results:
- Nanomedicine enables precise drug delivery and improved bioavailability for CAF targeting.
- Nanomaterials can be engineered for CAF depletion, reprogramming, or extracellular matrix remodeling.
- CAF-targeted nanoplatforms facilitate integrated diagnosis and therapy (theranostics).
Conclusions:
- Integrating CAF biology with nanotechnology holds transformative potential for overcoming PCa therapeutic resistance.
- Future directions include gene editing, multi-stimuli-responsive systems, and immunotherapy combinations for enhanced PCa treatment.
- Addressing CAF heterogeneity and nanomaterial biosafety are crucial for clinical translation.
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