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CMG2 Expression Is an Independent Prognostic Factor for Soft Tissue Sarcoma Patients
Thomas Greither1, Alice Wedler2, Swetlana Rot3
1Center for Reproductive Medicine and Andrology, Martin Luther University, 06120 Halle (Saale), Germany. thomas.greither@medizin.uni-halle.de.
International Journal of Molecular Sciences
|December 8, 2017
Summary
Capillary morphogenesis gene 2 (CMG2) expression is linked to soft tissue sarcoma patient survival. Low CMG2 levels indicate a poorer prognosis, suggesting CMG2
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Capillary morphogenesis gene 2 (CMG2), also known as anthrax toxin receptor 2 (ANTXR2), is a transmembrane protein involved in extracellular matrix adhesion and tissue remodeling.
- CMG2 influences endothelial cell proliferation and angiogenesis, and its reduced expression correlates with poorer survival in breast carcinoma patients.
Purpose of the Study:
- To investigate the expression of CMG2 mRNA and protein in soft tissue sarcoma (STS).
- To determine the association between CMG2 expression levels and patient outcomes in STS.
Main Methods:
- Quantitative real-time PCR was used to measure CMG2 mRNA in 121 STS tumor samples.
- Enzyme-linked immunosorbent assay (ELISA) was employed to quantify CMG2 protein in 52 STS tumor samples.
- Kaplan-Meier analysis was performed to assess the correlation between CMG2 expression and disease-specific survival.
Main Results:
- A significant positive correlation was observed between CMG2 mRNA and protein expression (r s = 0.31; p = 0.027).
- CMG2 mRNA expression correlated with genes involved in extracellular matrix remodeling, including CD26 and the uPA system.
- Low CMG2 mRNA expression was significantly associated with worsened disease-specific survival (25 vs. 96 months; p = 0.013), particularly in high-stage tumors.
Conclusions:
- Decreased CMG2 expression serves as a negative prognostic factor in soft tissue sarcoma.
- CMG2 represents a potential candidate for further research into the mechanisms of STS development and progression.

