In-depth characterization of miRNome in papillary thyroid cancer with BRAF V600E mutation
MicroRNAs (miRNAs) are small non-coding RNAs, which play a critical regulatory role in papillary thyroid carcinoma (PTC). BRAF V600E is a hotspot mutation occurring in a majority of PTC cases and is proposed to be associated with poor clinical outcomes. The relationship between BRAF V600E status a...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
2020
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| Subjects: | |
| Online Access: | http://eprints.unisza.edu.my/7358/1/FH02-FSK-20-45956.pdf http://eprints.unisza.edu.my/7358/ |
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| Summary: | MicroRNAs (miRNAs) are small non-coding RNAs, which play a critical regulatory role in papillary thyroid
carcinoma (PTC). BRAF V600E is a hotspot mutation occurring in a majority of PTC cases and is proposed to be associated
with poor clinical outcomes. The relationship between BRAF V600E status and miRNA expression in PTC has not been
comprehensively studied. In this study, we aimed to identify the differentially expressed miRNAs in PTCs with and without
BRAF V600E in an unbiased manner. Five fresh frozen thyroid cancer tissues paired with their respective adjacent normal
tissues from PTC patients were subjected to BRAF V600E genotyping using Sanger sequencing and small RNA deep
sequencing (miRNAseq). MiRNAs differentially expressed between BRAF V600E-positive and BRAF V600E-negative
PTC tissues were validated in silico using The Cancer Genome Atlas (TCGA) THCA datasets containing 420 samples.
MiRNA target prediction and pathway enrichment analysis were performed to identify biological pathways altered in this
cancer. We identified 174 differentially expressed miRNAs; 80 were significantly over-expressed, while 94 were underexpressed (adj. p-value < 0.1; log2 fold change ≤ -1 or ≥ 1). Fifteen miRNAs were significantly differentially expressed only
in BRAF V600E-positive PTC, and eight of these were validated in TCGA THCA dataset (hsa-miR-212, -132, -135b-3p/5p,
-200b, -200a-3p/5p, -27a-3p/5p, -29a and -1296). Subsequent analysis revealed significant enrichment of cancer-related
pathways including proteoglycans in cancer, ECM-receptor interaction and MAPK pathways in BRAF V600E-positive PTC.
Using the miRNAseq and in silico validation using TCGA THCA study, we identified eight miRNAs that were differentially
expressed in PTC tissues with BRAF V600E. This study also complemented the existing knowledge about deregulated
miRNAs in PTC development. |
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