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The Updated Status and Future Direction of Immunotherapy Targeting B7-H1/PD-1 in Osteosarcoma
Meng-Ke Fan1,2, Li-Li Qi3, Qi Zhang2
1Department of Orthopedic Oncology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Abstract:
Although the mortality rate of osteosarcoma (OS) patients has improved, there are still many unsolved problems concerning how to reduce recurrence and metastasis. In the tumor microenvironment, immune escape plays a more important role in tumor progression and development. Many costimulatory molecules of the B7 family have been reported to be involved in regulating immunological interactions between OS cells and immune cells. Among these molecules, B7-H1 and its receptor, programmed death-1 (PD-1), have been the focus of the fields of tumor immunology and have been recently applied in clinical trials of therapies for several solid tumors. These therapies, referred to as B7-H1/PD-1 checkpoint blockade therapies, are designed to block the interaction between the two molecules. Although the mechanism has been reported in some malignancies, the specific impact of B7-H1/PD-1 expression on OS has not been well defined. Here, we review the expression, function, and regulatory mechanism of the B7-H1/PD-1 axis in OS and introduce and compare the advantages and disadvantages of B7-H1/PD-1 immunotherapies in OS.
Insights
Immune escape via the B7-H1/programmed death-1 (PD-1) axis is crucial in osteosarcoma (OS) progression. Understanding this interaction and B7-H1/PD-1 immunotherapies is key to reducing OS recurrence and metastasis.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Osteosarcoma (OS) recurrence and metastasis remain significant challenges despite improved survival rates.
- Immune escape within the tumor microenvironment is a critical factor in OS progression.
- The B7 family of costimulatory molecules regulates immune cell interactions in OS.
Purpose of the Study:
- To review the expression, function, and regulation of the B7-H1/programmed death-1 (PD-1) axis in osteosarcoma.
- To compare the advantages and disadvantages of B7-H1/PD-1 immunotherapies for OS.
Main Methods:
- Literature review of B7-H1/PD-1 axis expression and function in osteosarcoma.
- Analysis of current B7-H1/PD-1 checkpoint blockade therapies in various malignancies.
- Comparative assessment of immunotherapy strategies for OS.
Main Results:
- The B7-H1/PD-1 axis plays a significant role in immune evasion in osteosarcoma.
- B7-H1/PD-1 checkpoint blockade therapies show promise but require further investigation in OS.
- Understanding the specific impact of B7-H1/PD-1 on OS is not yet well-defined.
Conclusions:
- The B7-H1/PD-1 axis is a critical target for overcoming immune escape in osteosarcoma.
- Further research is needed to optimize B7-H1/PD-1 immunotherapies for osteosarcoma treatment.
- Targeting the B7-H1/PD-1 pathway offers potential for reducing osteosarcoma recurrence and metastasis.
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