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Series GSE185719 Query DataSets for GSE185719
Status Public on Nov 23, 2021
Title MiRNA Deregulation Distinguishes Anaplastic Thyroid Carcinoma (ATC) and Supports Upregulation of Oncogene Expression
Organism Homo sapiens
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary Anaplastic thyroid carcinoma (ATC) is the most fatal and rapidly evolving endocrine malignancy invading the head and neck region and accounting for the majority of thyroid cancer-associated deaths. Deregulation of microRNA (miRNA) expression promotes thyroid carcinoma progression by modulating reorganization of the ATC transcriptome. Here, we applied comparative miRNA-/mRNA-sequencing in a cohort of 28 thyroid carcinomas to unravel the association of deregulated miRNA and mRNA expression. This identifies 85 miRNAs significantly deregulated in ATC. By establishing a new analysis pipeline we unravel 85 prime miRNA-mRNA interactions supporting the downregulation of candidate tumor-suppressors and upregulation of bona fide oncogenes like survivin (BIRC5) in ATC. This miRNA-dependent reprogramming of the ATC
transcriptome provides a mRNA signature comprising 65 genes sharply distinguishing ATC from other thyroid carcinomas. Validation of deregulated protein expression in an independent thyroid carcinoma cohort demonstrates that miRNA-dependent oncogenes comprised in this signature, the transferrin receptor TFRC (CD71) and the E3-ubiquitin ligase DTL, are sharply upregulated in ATC. This upregulation is even sufficient to distinguish ATC from partially differentiated thyroid carcinomas (PDTC). In sum, these findings provide new diagnostic tools and a robust resource to explore key miRNA-mRNA regulation underlying the progression of thyroid carcinoma.
 
Overall design Small RNA sequencing of the miRNA-transcriptome from 28 primary thyroid tumor samples
 
Contributor(s) Misiak D, Bauer M, Lange J, Haase J, Braun J, Lorenz K, Wickenhauser C, Hüttelmaier S
Citation(s) 34885022
Submission date Oct 12, 2021
Last update date Dec 15, 2021
Contact name Danny Misiak
E-mail(s) danny.misiak@medizin.uni-halle.de
Phone +49345573962
Organization name Martin Luther University Halle-Wittenberg
Department Molecular Cell Biology
Lab Hüttelmaier Lab
Street address Kurt-Mothes-Str. 3a
City Halle (Saale)
ZIP/Postal code 06120
Country Germany
 
Platforms (1)
GPL15456 Illumina HiScanSQ (Homo sapiens)
Samples (28)
GSM5622013 A1
GSM5622014 A2
GSM5622015 A3
Relations
BioProject PRJNA770622
SRA SRP341002

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Supplementary file Size Download File type/resource
GSE185719_DE_Thyroid_miRNA_ATC_FTC_PTC_NT_Others.csv.gz 163.1 Kb (ftp)(http) CSV
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Raw data are available in SRA
Processed data are available on Series record

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