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PD-1 and PD-L1 expression in bone and soft tissue sarcomas
Alireza Torabi1, Clarissa N Amaya2, Frank H Wians1
1Department of Pathology, Texas Tech University Health Sciences Center, Paul L. Foster School of Medicine, El Paso, Texas, United States.
Pathology
|July 10, 2017
Summary
This study found Programmed cell death protein 1 (PD-1) is overexpressed in bone and soft tissue sarcomas, but its ligand PD-L1 is largely absent. This suggests potential challenges for current PD-1/PD-L1 targeted immunotherapies in these cancers.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Programmed cell death protein 1 (PD-1) and its ligands are crucial in tumor immune evasion.
- Anti-PD-1 inhibitors are approved for several cancers, but their role in bone and soft tissue sarcomas is understudied.
- Expression of PD-1 and PD-L1 in various sarcoma subtypes needs further investigation.
Purpose of the Study:
- To evaluate the expression of PD-1 and its ligand PD-L1 in malignant bone and soft tissue sarcomas.
- To compare PD-1 and PD-L1 expression in sarcomas with normal tissues and benign counterparts.
- To assess PD-1 and PD-L1 protein levels in sarcoma cell lines.
Main Methods:
- Tissue microarrays of liposarcomas, rhabdomyosarcomas, osteosarcomas, and chondrosarcomas were stained for PD-1 and PD-L1.
- Normal adipose tissue, skeletal muscle, bone, osteochondroma, and lipoma served as controls.
- Western blot analysis was performed on four sarcoma cell lines.
Main Results:
- Osteosarcomas, chondrosarcomas, liposarcomas, and rhabdomyosarcomas overexpressed PD-1 compared to normal tissues.
- PD-1 expression in rhabdomyosarcomas correlated with higher tumor stage.
- PD-L1 expression was rare, found only in a few specific sarcoma subtypes; normal tissues were negative.
Conclusions:
- Bone and soft tissue sarcomas exhibit significant cytoplasmic PD-1 expression.
- PD-L1 expression is minimal to absent in these sarcomas.
- The limited PD-L1 expression raises questions about the efficacy of current PD-1/PD-L1 targeted immunotherapies for these malignancies.

