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Exploring shared targets in cancer immunotherapy and cancer-induced bone pain: Insights from preclinical studies
Ruofan Zhang1, Yachen Yang1, Xiang Li2
1Department of Integrative Medicine and Neurobiology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Abstract:
Cancer casts a profound shadow on global health, with pain emerging as one of the dominant and severe complications, particularly in advanced stages. The effective management of cancer-induced pain remains an unmet need. Emerging preclinical evidence suggests that targets related to tumor immunotherapy may also modulate cancer-related pain pathways, thus offering a promising therapeutic direction. This review, focusing on more than ten molecular targets that link cancer immunotherapy and cancer-induced bone pain, underscores their potential to tackle both aspects in the context of comprehensive cancer care. Emphasizing factors such as types of cancer, drug administration methods, and sex differences in the analgesic efficacy of immunotherapeutic agents provides neuroscientific insights into personalized pain management for patients with cancer.
Insights
Cancer immunotherapy targets may also treat cancer pain. This review highlights over ten molecular targets linking cancer immunotherapy and bone pain, offering new avenues for personalized cancer pain management.
Area of Science:
- Oncology
- Neuroscience
- Immunology
Background:
- Cancer is a global health issue, with severe pain being a common complication, especially in advanced stages.
- Effective management of cancer-induced pain is a significant unmet clinical need.
- Preclinical research suggests a link between tumor immunotherapy targets and cancer pain pathways.
Purpose of the Study:
- To review molecular targets that connect cancer immunotherapy and cancer-induced bone pain.
- To explore the potential of these targets in addressing both cancer progression and pain.
- To provide neuroscientific insights for personalized pain management in cancer patients.
Main Methods:
- Literature review of preclinical evidence.
- Focus on over ten molecular targets linking cancer immunotherapy and cancer-induced bone pain.
- Analysis of factors influencing analgesic efficacy, including cancer type, administration, and sex differences.
Main Results:
- Identified multiple molecular targets with potential to modulate both cancer and pain pathways.
- Highlighted the promise of targeting these pathways for comprehensive cancer care.
- Emphasized the role of cancer type, drug delivery, and sex in analgesic outcomes.
Conclusions:
- Targets linking cancer immunotherapy and cancer-induced bone pain offer a promising dual therapeutic approach.
- Understanding these targets can lead to more personalized and effective pain management strategies for cancer patients.
- Further research into sex differences and administration methods is crucial for optimizing immunotherapeutic pain relief.
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