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PIWI 相互作用 RNA piR-13643 和 piR-21238 是甲状腺乳头状癌有前途的诊断生物标志物。

PIWI-interacting RNAs piR-13643 and piR-21238 are promising diagnostic biomarkers of papillary thyroid carcinoma.

机构信息

Department of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.

Division of Spine, Department of Orthopedics, Tongji Hospital Affiliated to Tongji University School of Medicine, Shanghai, China.

出版信息

Aging (Albany NY). 2020 May 19;12(10):9292-9310. doi: 10.18632/aging.103206.

Abstract

Emerging studies demonstrate that PIWI-interacting RNAs (piRNAs) participate in the development of cancers. 75 pairs of papillary thyroid carcinoma (PTC) samples and 31 benign thyroid nodule samples were included in this three-phase biomarker identifying study. First, piRNA expression profiles of five pairs of PTC samples were acquired piRNA sequencing. The expression of all upregulated piRNAs were further validated by RT-qPCR. Paired t and nonparametric test were used to evaluate the association between all upregulated piRNAs and clinic stage. The expression levels of key piRNAs were corrected by demographic data to construct a multivariate model to distinguish malignant nodules from benign. Additionally, the intersection between target genes of key piRNAs and differentially expressed genes in The Cancer Genome Atlas (TCGA) PTC samples were used to perform enrichment analysis. Only piR-13643 and piR-21238 were significantly upregulated in PTC and associated with clinic stage. Moreover, both piR-13643 (Area Under Curve (AUC): 0.821) and piR-21238 (AUC: 0.823) showed better performance in distinguishing malignant nodules from benign than currently used biomarkers HBME1 (AUC: 0.590). Based on our findings, piR-13643 and piR-21238 were observed to be significantly upregulated in human PTC. PIWI-interacting RNAs could serve as promising novel biomarkers for accurate detection of PTC.

摘要

新兴研究表明,PIWI 相互作用 RNA(piRNA)参与癌症的发展。本研究采用三阶段生物标志物识别方法,纳入了 75 对甲状腺乳头状癌(PTC)样本和 31 例良性甲状腺结节样本。首先,通过 piRNA 测序获得了五对 PTC 样本的 piRNA 表达谱。所有上调的 piRNA 的表达均通过 RT-qPCR 进一步验证。配对 t 检验和非参数检验用于评估所有上调的 piRNA 与临床分期之间的相关性。通过人口统计学数据校正关键 piRNA 的表达水平,构建多变量模型以区分恶性结节和良性结节。此外,还使用关键 piRNA 的靶基因与癌症基因组图谱(TCGA)PTC 样本中差异表达基因的交集进行富集分析。只有 piR-13643 和 piR-21238 在 PTC 中显著上调,并与临床分期相关。此外,piR-13643(AUC:0.821)和 piR-21238(AUC:0.823)在区分良恶性结节方面的表现均优于目前使用的标志物 HBME1(AUC:0.590)。基于我们的发现,piR-13643 和 piR-21238 在人类 PTC 中观察到显著上调。PIWI 相互作用 RNA 可能成为准确检测 PTC 的有前途的新型生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e520/7288952/5edae0c18937/aging-12-103206-g001.jpg

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