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Journal ArticleDOI

Circulating serum miRNAs as potential biomarkers for nephroblastoma

TLDR
Preoperative chemotherapy without histological confirmation by biopsy without minimal‐invasive diagnostic markers confirming nephroblastoma diagnosis are highly warranted.
Abstract
Background Nephroblastoma (or Wilms tumor—WT) is the most common childhood kidney cancer. In Europe, nephroblastoma is treated with preoperative chemotherapy without histological confirmation by biopsy. Therefore, minimal-invasive diagnostic markers confirming nephroblastoma diagnosis are highly warranted. Procedure In our study, we aim to identify circulating miRNAs with diagnostic potential for differentiating nephroblastoma from controls. We determined the level of 19 miRNAs in serum of 32 patients with nephroblastoma and 12 controls with quantitative real-time PCR. Three miRNAs were further tested in an independent validation set including sera of patients with renal tumors other than Wilms. Results In total, 14 miRNAs showed significantly higher abundance in serum of patients with nephroblastoma than in controls. The miRNAs with highest diagnostic potentials included miRs-130b-3p, -100-5p, and -143-3p with an AUC of 0.94, 0.90, and 0.89, respectively. A signature based on these three miRNAs to differentiated patients from controls with an accuracy of 84.58%, a sensitivity of 76.67%, and a specificity of 92.5%. Higher expression of miRs-100-5p and -130b-3p was confirmed in an independent validation set. The signature based on miRs-100-5p and -130b-3p differentiated patients with nephroblastoma from healthy controls with an accuracy, sensitivity, and specificity of 79.6%, 69.2%, and 90.0%, respectively. Conclusion In summary, we provide first evidence that serum miR-100-5p and -130b-3p hold potential as biomarker for WT irrespective of the subtype and that expression level of these miRNA in serum is unaffected by differences in serum collection. Pediatr Blood Cancer 2015;62:1360–1367. © 2015 Wiley Periodicals, Inc.

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Journal ArticleDOI

An estimate of the total number of true human miRNAs.

TL;DR: The experimentally validated miRNAs will contribute to revising targetomes hypothesized by utilizing falsely annotated miRNA candidates, 1115 of which are currently annotated in miRBase V22.
Journal ArticleDOI

A pipeline to quantify serum and cerebrospinal fluid microRNAs for diagnosis and detection of relapse in paediatric malignant germ-cell tumours

TL;DR: A robust technical pipeline to quantify miRNAs in the serum and cerebrospinal fluid and allowed early detection of relapse of a testicular mixed malignant GCT; and distinguished intracranial malignantGCT from intrac Cranial non-GCT tumours at diagnosis, using CSF and serum samples are developed.
Journal ArticleDOI

The translational potential of microRNAs as biofluid markers of urological tumours

TL;DR: Qualitative and analytical pitfalls exist and require addressing to enable future translation of the laboratory findings regarding miRNAs as biomarkers into clinical practice in bladder cancer, kidney cancer, prostate cancer and testicular cancer.
Journal ArticleDOI

Biology and treatment of renal tumours in childhood.

TL;DR: Ongoing collaboration is needed to ensure consistency of outcomes through standardised diagnostics and treatment and incorporation of biomarker research, which constitute the rationale for the forthcoming SIOP-RTSG 'UMBRELLA' study.
References
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Journal ArticleDOI

MicroRNAs: Genomics, Biogenesis, Mechanism, and Function

TL;DR: Although they escaped notice until relatively recently, miRNAs comprise one of the more abundant classes of gene regulatory molecules in multicellular organisms and likely influence the output of many protein-coding genes.
Journal ArticleDOI

Assessing sample and miRNA profile quality in serum and plasma or other biofluids

TL;DR: Normal reference ranges for circulating miRNAs in serum and plasma as well as a hemolysis indicator based on microRNA expression are developed.
Journal ArticleDOI

Haemolysis during sample preparation alters microRNA content of plasma.

TL;DR: It is found that levels of miR-16, a commonly used reference gene, showed little variation when measured in plasma samples from healthy volunteers or patients with malignant mesothelioma or coronary artery disease, and increases in plasma miR -16 andMiR-451 are caused by haemolysis.
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