Biomimetic bone niche reconstructs proliferation-inhibited and therapy-resistant bone-metastatic prostate cancer

Prostate cancer bone metastases often harbor a rare subset of tumor cells with suppressed proliferation, contributing to therapy resistance and disease relapse. However, the lack of physiologically relevant <i>in vitro</i> models has hindered mechanistic and therapeutic advances. Here, we engineered a 3D bone-like microenvironment by integrating calcium phosphate scaffolds, decellularized extracellular matrix (dECM), mesenchymal stem cells (MSCs), and osteoblasts. This biomimetic niche induced a proliferation-inhibited state in prostate cancer cells, closely mirroring transcriptomic signatures identified from patient-derived single-cell RNA sequencing datasets. Tumor cells in this niche also displayed enzalutamide resistance, accompanied by metabolic reprogramming and activation of pro-survival signaling. This platform provides a clinically relevant tool for modeling bone metastatic prostate cancer and accelerating the development of therapies targeting resistant tumor states.

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Publication Details

Journal
Bioactive Materials
Published
2025-10-15
DOI
https://doi.org/10.1016/j.bioactmat.2025.09.041
Citations
1
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
1.52
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article

Biomimetic bone niche reconstructs proliferation-inhibited and therapy-resistant bone-metastatic prostate cancer

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1 citations
Bioactive Materials
Prostate Cancer Treatment and Research
1.52
article

Biomimetic bone niche reconstructs proliferation-inhibited and therapy-resistant bone-metastatic prostate cancer

Yu Luo, Yan Peng, Ying Zhao, Zhongte Peng, Qijun Lin, Lianheng Chen, Huiling Liu, Chun Liu, Xin Chen, Jianfeng Huang, Lei Yang, Xinsheng Peng, Xuenong Zou, Xihong Fu
article en
1 citations

Abstract

Prostate cancer bone metastases often harbor a rare subset of tumor cells with suppressed proliferation, contributing to therapy resistance and disease relapse. However, the lack of physiologically relevant <i>in vitro</i> models has hindered mechanistic and therapeutic advances. Here, we engineered a 3D bone-like microenvironment by integrating calcium phosphate scaffolds, decellularized extracellular matrix (dECM), mesenchymal stem cells (MSCs), and osteoblasts. This biomimetic niche induced a proliferation-inhibited state in prostate cancer cells, closely mirroring transcriptomic signatures identified from patient-derived single-cell RNA sequencing datasets. Tumor cells in this niche also displayed enzalutamide resistance, accompanied by metabolic reprogramming and activation of pro-survival signaling. This platform provides a clinically relevant tool for modeling bone metastatic prostate cancer and accelerating the development of therapies targeting resistant tumor states.

Bioactive MaterialsVol. 56
University of Shanghai for Science and Technology (CN), Sun Yat-sen University (CN), Hebei University of Technology (CN), Soochow University (CN), The First Affiliated Hospital, Sun Yat-sen University (CN), First Affiliated Hospital of Soochow University (CN)
Openalex Percentile: Top 14%
Prostate Cancer Treatment and Research
1.52
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