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Identification of miRNAs and Their Target Genes Associated with Sunitinib Resistance in Clear Cell Renal Cell Carcinoma Patients
被引:0
|作者:
Armesto, Maria
[1
]
Nemours, Stephane
[1
]
Arestin, Maria
[1
]
Bernal, Iraide
[1
,2
]
Solano-Iturri, Jon Danel
[2
]
Manrique, Manuel
[2
]
Basterretxea, Laura
[1
,3
]
Larrinaga, Gorka
[4
,5
]
Angulo, Javier C.
[6
,7
]
Lecumberri, David
[8
]
Iturregui, Ane Miren
[9
]
Lopez, Jose I.
[4
,10
]
Lawrie, Charles H.
[1
,11
,12
]
机构:
[1] Biogipuzkoa Hlth Res Inst, Mol Oncol Grp, San Sebastian 20014, Spain
[2] Donostia Univ Hosp, Pathol Dept, San Sebastian 20014, Spain
[3] Donostia Univ Hosp, Med Oncol Dept, San Sebastian 20014, Spain
[4] Biobizkaia Hlth Res Inst, Baracaldo 48903, Spain
[5] Univ Basque Country UPV EHU, Fac Med & Nursing, Dept Physiol, Leioa 48940, Spain
[6] European Univ Madrid, Fac Med Sci, Clin Dept, Getafe 28905, Spain
[7] Univ Hosp Getafe, Dept Urol, Madrid 28907, Spain
[8] Urduliz Univ Hosp, Dept Urol, Urduliz 48610, Spain
[9] Cruces Univ Hosp, Dept Urol, Baracaldo 48903, Spain
[10] Cruces Univ Hosp, Pathol Dept, Baracaldo 48903, Spain
[11] IKERBASQUE, Basque Fdn Sci, Bilbao 48009, Spain
[12] Univ Oxford, Radcliffe Dept Med, Oxford OX3 9DU, England
关键词:
renal cancer;
sunitinib;
resistance;
miRNA;
transcriptome;
pathway analysis;
CANCER STATISTICS;
PROGNOSTIC MODEL;
DENDRITIC CELLS;
IN-SITU;
MICRORNA;
EXPRESSION;
MIR-155;
PROLIFERATION;
GLIOBLASTOMA;
VALIDATION;
D O I:
10.3390/ijms25136881
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页数:23
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