miRNA Profiles as a Predictor of Chemoresponsiveness in Wilms' Tumor Blastema

被引:66
作者
Watson, Jenny A. [1 ]
Bryan, Kenneth [2 ]
Williams, Richard [3 ]
Popov, Sergey [4 ]
Vujanic, Gordan [5 ]
Coulomb, Aurore [6 ]
Boccon-Gibod, Liliane [6 ]
Graf, Norbert [7 ]
Pritchard-Jones, Kathy [3 ]
O'Sullivan, Maureen [1 ,8 ]
机构
[1] Our Ladys Childrens Hosp, Natl Childrens Res Ctr, Dublin, Ireland
[2] Royal Coll Surgeons Ireland, Dublin 2, Ireland
[3] UCL Inst Child Hlth, London, England
[4] Inst Canc Res, Surrey, England
[5] Cardiff Univ, Sch Med, Cardiff, S Glam, Wales
[6] Univ Paris 06, Hop Armand Trousseau, Paris, France
[7] Univ Saarland, Dept Pediat Oncol & Hematol, Homburg, Germany
[8] Our Ladys Childrens Hosp, Dept Pathol, Dublin, Ireland
关键词
TAMOXIFEN RESISTANCE; MICRORNAS; CANCER; NEPHROBLASTOMA; CHEMOTHERAPY; TRIAL; GENE;
D O I
10.1371/journal.pone.0053417
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The current SIOP treatment protocol for Wilms' tumor involves pre-operative chemotherapy followed by nephrectomy. Not all patients benefit equally from such chemotherapy. The aim of this study was to generate a miRNA profile of chemo resistant blastemal cells in high risk Wilms' tumors which might serve as predictive markers of therapeutic response at the pre-treatment biopsy stage. We have shown here that unsupervised hierarchical clustering of genome-wide miRNA expression profiles can clearly separate intermediate risk tumors from high risk tumors. A total of 29 miRNAs were significantly differentially expressed between post-treatment intermediate risk and high risk groups, including miRNAs that have been previously linked to chemo resistance in other cancer types. Furthermore, 7 of these 29 miRNAs were already at the pre-treatment biopsy stage differentially expressed between cases ultimately deemed intermediate risk compared to high risk. These miRNA alterations include down-regulation in high risk cases of miR-193a. 5p, miR-27a and the up-regulation of miR-483.5p, miR-628.5p, miR-590.5p, miR-302a and miR-367. The demonstration of such miRNA markers at the pretreatment biopsy stage could permit stratification of patients to more tailored treatment regimens.
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页数:7
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