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Updated: Jan 25, 2026

Models of Bone Metastasis
Published on: September 4, 2012
Osteopontin as a multifaceted driver of bone metastasis and drug resistance
Xiaocong Pang1, Kan Gong2, Xiaodan Zhang1
1Department of Pharmacy, Peking University First Hospital, Xicheng District, 10034, Beijing, China.
Abstract:
Metastasis to bone frequently occurs in majority of patients with advanced breast cancer and prostate cancer, leading to devastating skeletal-related events and substantially reducing the survival of patients. Currently, the crosstalk between tumor cells and the bone stromal compartment was widely investigated for bone metastasis and the resistance to many conventional therapeutic methods. Osteopontin (OPN), also known as SPP1 (secreted phosphoprotein 1), a secreted and chemokine-like glyco-phosphoprotein is involved in tumor progression such as cell proliferation, angiogenesis, and metastasis. The expression of OPN in tumor tissue and plasma has been clinically proved to be correlated to poor prognosis and shortened survival in patients with breast cancer and prostate cancer. This review summarizes the multifaceted roles that OPN plays in bone microenvironment and drug resistance, with emphasis on breast and prostate cancers, via binding to αvβ3 integrin and CD44 receptor and inducing signaling cascades. We further discuss the promising therapeutic strategy for OPN targeting, mainly inhibiting OPN at transcriptional or protein level or blocking it binding to receptor or its downstream signaling pathways. The comprehending of the function of OPN in bone microenvironment is crucial for the development of novel biomarker and potential therapeutic target for the diagnosis and treatment of bone metastasis and against the emergence of drug resistance in advanced cancers.
Insights
Osteopontin (OPN) drives bone metastasis in advanced breast and prostate cancers by interacting with tumor cells and the bone microenvironment. Targeting OPN offers a promising strategy to combat cancer spread and overcome drug resistance.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Bone metastasis is a common complication in advanced breast and prostate cancers, leading to poor prognosis.
- Tumor cell interactions with the bone microenvironment contribute to metastasis and therapeutic resistance.
- Osteopontin (OPN), also known as SPP1, is implicated in tumor progression, including proliferation, angiogenesis, and metastasis.
Purpose of the Study:
- To review the roles of Osteopontin (OPN) in the bone microenvironment and drug resistance.
- To emphasize OPN's involvement in breast and prostate cancer bone metastasis.
- To discuss potential therapeutic strategies targeting OPN.
Main Methods:
- Literature review summarizing existing research on Osteopontin (OPN).
- Analysis of OPN's interactions with receptors like αvβ3 integrin and CD44.
- Discussion of signaling pathways induced by OPN.
Main Results:
- OPN expression in tumor tissue and plasma correlates with poor prognosis in breast and prostate cancer patients.
- OPN promotes tumor progression and metastasis through interactions with bone stromal cells.
- OPN contributes to resistance against conventional therapies.
Conclusions:
- Understanding OPN's function in the bone microenvironment is critical for developing new therapeutic targets.
- Targeting OPN at various levels (transcription, protein, receptor binding, downstream signaling) shows therapeutic potential.
- OPN represents a promising biomarker and therapeutic target for bone metastasis and drug resistance in advanced cancers.
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