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Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Increased concentrations of transforming growth factor beta1 and beta2 in the plasma of patients with glioblastoma
Thomas Schneider1, Michael Sailer, Siegfried Ansorge
1Department of Neurosurgery, Otto-von-Guericke University, Leipziger Strasse 44, D-39120, Magdeburg, Germany, thomas.schneider@medizin.uni-magdeburg.de.
Abstract:
Recently, several in vitro studies have demonstrated production of the potent immunosuppressive cytokine transforming growth factor beta (TGF-beta)2 in glioblastoma cell lines. Systematic studies of the concentration of TGF-beta isoforms in the plasma of patients harboring intracerebral tumors do not exist. In the present study, the concentrations of TGF-beta1 and TGF-beta2 in platelet-poor plasma of 21 patients with glioblastoma before and after extensive resection were measured by specific ELISA systems and related to survival. The plasma concentrations of latent TGF-beta1 of patients with glioblastoma prior to surgery were significantly higher in comparison to healthy control probands, but not to patients with multiple sclerosis (MS). Furthermore, latent TGF-beta2 was found to be significantly increased in the plasma of patients with glioblastoma in comparison to healthy control probands and patients with MS. After extensive resection of the tumor, the value of latent TGF-beta2 evidently decreased. Interestingly, the concentration of latent TGF-beta2 prior to surgery was correlated with survival and a strong relationship was found between the survival and the difference of latent TGF-beta2 levels prior to surgery minus the TGF-beta2 concentrations 7 days after surgery. A higher difference in these plasma concentrations >6 ng/ml vs. <6 ng/ml clearly correlates with a longer survival time. In conclusion, this study suggests that glioblastoma does secret TGF-beta2 in vivo and that TGF-beta2 may play an important role in glioblastoma patients.
Insights
Glioblastoma patients show elevated levels of transforming growth factor beta (TGF-beta)2. Lowering TGF-beta2 after surgery correlates with longer survival, suggesting its role in glioblastoma progression.
Area of Science:
- Neuro-oncology
- Immunology
- Biochemistry
Background:
- Transforming growth factor beta (TGF-beta)2, an immunosuppressive cytokine, is produced in glioblastoma cell lines.
- Systematic studies on TGF-beta isoform concentrations in the plasma of patients with intracerebral tumors are lacking.
Purpose of the Study:
- To measure TGF-beta1 and TGF-beta2 plasma concentrations in glioblastoma patients before and after surgery.
- To correlate these concentrations with patient survival.
Main Methods:
- ELISA systems were used to quantify latent TGF-beta1 and TGF-beta2 in platelet-poor plasma from 21 glioblastoma patients and control groups.
- Measurements were taken before and after tumor resection.
Main Results:
- Plasma concentrations of latent TGF-beta1 were higher in glioblastoma patients than in healthy controls, but not different from multiple sclerosis patients.
- Latent TGF-beta2 was significantly increased in glioblastoma patients compared to both healthy controls and MS patients.
- Latent TGF-beta2 levels decreased after tumor resection.
- Pre-surgery latent TGF-beta2 concentration correlated with survival.
- A significant relationship was found between survival and the difference in latent TGF-beta2 levels before and 7 days after surgery; a difference >6 ng/ml correlated with longer survival.
Conclusions:
- Glioblastoma secretes TGF-beta2 in vivo.
- TGF-beta2 may play a significant role in glioblastoma pathogenesis and patient outcomes.

