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Published on: July 3, 2020
CD138 (syndecan-1) expression in bone-forming tumors
Amberly L Nunez1, Gene P Siegal, Vishnu V B Reddy
1Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35249-7331, USA.
American Journal of Clinical Pathology
|February 17, 2012
Summary
CD138 (syndecan-1) is not a reliable marker for plasmacytic origin in bone tumors. Researchers found CD138 expression in osteosarcomas and benign bone tumors, but not in other bone lesions.
Area of Science:
- Oncology
- Pathology
- Biomarker Research
Background:
- CD138 (syndecan-1) is a cell surface proteoglycan crucial for identifying plasmacytic differentiation in hematologic disorders.
- While CD138 expression is noted in epithelial and soft tissue neoplasms, its role in bone tumors remains largely unevaluated.
Purpose of the Study:
- To investigate CD138 expression in various primary bone tumors and reactive bone lesions.
- To determine if CD138 can serve as a specific marker for plasmacytic differentiation in bone neoplasms.
Main Methods:
- CD138 expression was assessed immunohistochemically in 27 osteosarcomas, 12 benign bone-forming tumors, and 17 reactive bone cases.
- A tissue microarray (TMA) of 24 osteosarcomas, 24 chondrosarcomas, 12 giant cell tumors, and 9 normal bone samples was also analyzed for CD138.
- Immunoglobulin kappa and lambda stains were performed on CD138-positive cases.
Main Results:
- CD138 was expressed in 52% of in-house osteosarcoma cases and 8% of TMA osteosarcoma cases, and in 83% of osteoid osteoma/osteoblastoma cases.
- No CD138 reactivity was observed in chondrosarcomas, giant cell tumors of bone, or normal/reactive bone samples.
- Immunoglobulin stains were negative in all CD138-positive bone tumor cases, ruling out plasmacytic origin.
Conclusions:
- CD138 expression in bone tumors does not reliably indicate plasmacytic differentiation.
- Caution is advised when interpreting CD138-positive cells in bony lesions without established hematologic etiology.
- CD138 is not a definitive marker for plasma cell neoplasms in bone.