Identification of miRNAs and Their Target Genes Associated with Sunitinib Resistance in Clear Cell Renal Cell Carcinoma Patients.
María ArmestoStéphane NemoursMaría ArestinIraide BernalJon Danel Solano-IturriManuel ManriqueLaura BasterretxeaGorka LarrinagaJavier C AnguloDavid LecumberriAne Miren IturreguiJose Ignacio LópezCharles Henderson LawriePublished in: International journal of molecular sciences (2024)
Sunitinib has greatly improved the survival of clear cell renal cell carcinoma (ccRCC) patients in recent years. However, 20-30% of treated patients do not respond. To identify miRNAs and genes associated with a response, comparisons were made between biopsies from responder and non-responder ccRCC patients. Using integrated transcriptomic analyses, we identified 37 miRNAs and 60 respective target genes, which were significantly associated with the NF-kappa B, PI3K-Akt and MAPK pathways. We validated expression of the miRNAs ( miR-223 , miR-155 , miR-200b , miR-130b ) and target genes ( FLT1 , PRDM1 and SAV1 ) in 35 ccRCC patients. High levels of miR-223 and low levels of FLT1 , SAV1 and PRDM1 were associated with worse overall survival (OS), and combined miR-223 + SAV1 levels distinguished responders from non-responders (AUC = 0.92). Using immunohistochemical staining of 170 ccRCC patients, VEGFR1 ( FLT1 ) expression was associated with treatment response, histological grade and RECIST (Response Evaluation Criteria in Solid Tumors) score, whereas SAV1 and BLIMP1 ( PRDM1 ) were associated with metachronous metastatic disease. Using in situ hybridisation (ISH) to detect miR-155 we observed higher tumoural cell expression in non-responders, and non-tumoural cell expression with increased histological grade. In summary, our preliminary analysis using integrated miRNA-target gene analyses identified several novel biomarkers in ccRCC patients that surely warrant further investigation.
Keyphrases
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- cell proliferation
- peritoneal dialysis
- prognostic factors
- poor prognosis
- long non coding rna
- pi k akt
- squamous cell carcinoma
- dna methylation
- gene expression
- genome wide
- stem cells
- patient reported outcomes
- long noncoding rna
- toll like receptor
- binding protein
- patient reported
- rna seq