| Literature DB >> 32504411 |
Marika Sciandra1, Alessandra De Feo2, Alessandro Parra1, Lorena Landuzzi1, Pier-Luigi Lollini3, Maria Cristina Manara1, Gianfranco Mattia4, Giada Pontecorvi4, Cristina Baricordi1, Clara Guerzoni1, Alberto Bazzocchi5, Alessandra Longhi6, Katia Scotlandi7.
Abstract
Appropriate tools for monitoring sarcoma progression are still limited. The aim of the present study was to investigate the value of miR-34a-5p (miR34a) as a circulating biomarker to follow disease progression and measure the therapeutic response. Stable forced re-expression of miR34a in Ewing sarcoma (EWS) cells significantly limited tumor growth in mice. Absolute quantification of miR34a in the plasma of mice and 31 patients showed that high levels of this miRNA inversely correlated with tumor volume. In addition, miR34a expression was higher in the blood of localized EWS patients than in the blood of metastatic EWS patients. In 12 patients, we followed miR34a expression during preoperative chemotherapy. While there was no variation in the blood miR34a levels in metastatic patients at the time of diagnosis or after the last cycle of preoperative chemotherapy, there was an increase in the circulating miR34a levels in patients with localized tumors. The three patients with the highest fold-increase in the miR levels did not show evidence of metastasis. Although this analysis should be extended to a larger cohort of patients, these findings imply that detection of the miR34a levels in the blood of EWS patients may assist with the clinical management of EWS.Entities:
Keywords: Circulating biomarkers; Ewing sarcoma; Metastases; miR34a; miRNAs
Year: 2020 PMID: 32504411 PMCID: PMC7511499 DOI: 10.1007/s12079-020-00567-2
Source DB: PubMed Journal: J Cell Commun Signal ISSN: 1873-9601 Impact factor: 5.782