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Platelet-derived growth factor expression and stimulation in human meningiomas
P M Black1, R Carroll, D Glowacka
1Brain Tumor Center, Brigham and Women's Hospital, Boston, Massachusetts.
Journal of Neurosurgery
|September 1, 1994
Summary
Platelet-derived growth factor (PDGF) stimulates meningioma cell division. PDGF-A, PDGF-B, and PDGF-beta receptors are expressed in meningiomas, suggesting PDGF-BB acts as a growth factor in these tumors.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Meningiomas are primary tumors of the central nervous system.
- The platelet-derived growth factor (PDGF) family plays a role in cell growth and development.
- The role of PDGF-BB in meningioma pathogenesis is not fully understood.
Purpose of the Study:
- To investigate the expression of PDGF family members in meningiomas.
- To determine the effect of exogenous PDGF-BB on meningioma cell growth.
- To examine the functional activity of the PDGF-beta receptor in meningiomas.
Main Methods:
- Northern blot analysis of PDGF-A, PDGF-B, PDGF-alpha receptor, and PDGF-beta receptor mRNA expression in 20 meningioma tissues.
- In vitro culture of 10 human meningioma cell lines to assess growth response to PDGF-BB using tritiated thymidine incorporation.
- Western blot analysis to detect c-fos proto-oncogene induction by PDGF-BB.
Main Results:
- All meningioma samples expressed PDGF-A and PDGF-B mRNA. PDGF-beta receptor mRNA was detected in 19 out of 20 tumors, while PDGF-alpha receptor mRNA was not detected.
- Exogenous PDGF-BB significantly stimulated meningioma cell proliferation in 3 out of 10 tested specimens, with a 3- to 6-fold increase in thymidine incorporation.
- PDGF-BB induced a significant increase in c-fos protein levels in meningioma cell cultures within 3 hours, indicating functional PDGF-beta receptor activation.
Conclusions:
- Meningiomas express PDGF-A, PDGF-B subunits, and functional PDGF-beta receptors.
- PDGF-BB acts as a growth factor for a subset of meningiomas.
- These findings support the hypothesis that PDGF signaling contributes to meningioma development and progression.