MiR-155-5p and MiR-203a-3p Are Prognostic Factors in Soft Tissue Sarcoma.
Thomas GreitherFranziska KoserHans-Jürgen HolzhausenAntje GüttlerPeter WürlMatthias KapplerSven WachHelge TaubertPublished in: Cancers (2020)
Soft tissue sarcoma (STS) is a heterogeneous group of rare malignancies with a five-year survival rate of approximately 50%. Reliable molecular markers for risk stratification and subsequent therapy management are still needed. Therefore, we analyzed the prognostic potential of miR-155-5p and miR-203a-3p expression in a cohort of 79 STS patients. MiR-155-5p and miR-203a-3p expression was measured from tumor total RNA by qPCR and correlated with the demographic, clinicopathological, and prognostic data of the patients. Elevated miR-155-5p expression was significantly associated with increased tumor stage and hypoxia-associated mRNA/protein expression. High miR-155-5p expression and low miR-203a-3p expression, as well as a combination of high miR-155-5p and low miR-203a-3p expression, were significantly associated with poor disease-specific survival in STS patients in the Kaplan-Meier survival analyses (p = 0.027, p = 0.001 and p = 0.0003, respectively) and in the univariate Cox regression analyses (RR = 1.96; p = 0.031; RR = 2.59; p = 0.002 and RR = 4.76; p = 0.001, respectively), but not in the multivariate Cox regression analyses. In conclusion, the oncomiR miR-155-5p and the tumor suppressor-miR miR-203a-3p exhibit an association with STS patient prognosis and are suggested as candidates for risk assessment.
Keyphrases
- prognostic factors
- poor prognosis
- end stage renal disease
- risk assessment
- chronic kidney disease
- newly diagnosed
- long non coding rna
- binding protein
- peritoneal dialysis
- cell proliferation
- stem cells
- endothelial cells
- patient reported outcomes
- machine learning
- climate change
- electronic health record
- artificial intelligence
- free survival
- cell therapy
- replacement therapy