1. Searching for circulating microRNAs in genitourinary tumors
- Author
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Luis M. Antón Aparicio, Francisco Gómez Veiga, Guadalupe Aparicio Gallego, Manuel Valladares Ayerbes, Aurea Molina Diaz, Natalia Fernandez Nunez, Vanessa Medina Villaamil, Maria Quindós Varela, and Isabel Santamarina Cainzos
- Subjects
Cancer Research ,Genitourinary system ,business.industry ,medicine.disease ,Bioinformatics ,Circulating MicroRNA ,medicine.anatomical_structure ,Circulating tumor cell ,Oncology ,Renal cell carcinoma ,Tumor progression ,Prostate ,microRNA ,medicine ,Cancer research ,Clinical significance ,business - Abstract
468 Background: Detection of circulating tumor cells (CTC) may provide diagnostic and prognostic information in genitourinary tumors (GT). The aim of this work was identify aberrantly expressed miRNAs potentially useful for CTC detection in blood samples from patients with GT to assess their potential clinical significance, and to gain a greater understanding of the mechanisms driving tumor progression. Methods: We examined blood levels of 92 microRNAs in 113 metastatic patients: prostate (mP), renal cell carcinoma (mRCC), bladder tumors (mB) and healthy volunteers (HV) (N=18) using SYBR-green-based microRNA RT-qPCR arrays (Exiqon). Array design was made by literature review and bioinformatics approach using free databases. Relative Expression Software Tool (REST) and SPPS 21.0 were used to data processing and analysis. Results: microRNAs differential expressed between tumors and HV (only up-regulated miRNAs are shown in Table). Conclusions: microRNAs in the circulation are relatively stable, very accessible, low invasive and easily testable biomarkers. These results suggest that our bioinformatic approach is an useful high-throughput method to identified tumors-associated miRNAs. The selected miRNAs should be further evaluated for their potential as markers for CTC detection, prognosis and therapeutic outcome. Further studies of precision and sensitivity on these markers in this GT population will clarify its role as novel stable blood-based markers. [Table: see text]
- Published
- 2014