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鉴定肾透明细胞癌中的 microRNA 编辑位点。

Identification of microRNA editing sites in clear cell renal cell carcinoma.

机构信息

State Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, 650500, Yunnan, China.

College of Landscape and Horticulture, Yunnan Agricultural University, Kunming, 650201, Yunnan, China.

出版信息

Sci Rep. 2023 Sep 13;13(1):15117. doi: 10.1038/s41598-023-42302-y.

Abstract

Clear cell renal cell carcinoma (ccRCC) is a malignant tumor originating from the renal tubular epithelium. Although the microRNAs (miRNAs) transcriptome of ccRCC has been extensively studied, the role of miRNAs editing in ccRCC is largely unknown. By analyzing small RNA sequencing profiles of renal tissues of 154 ccRCC patients and 22 normal controls, we identified 1025 miRNA editing sites from 246 pre-miRNAs. There were 122 editing events with significantly different editing levels in ccRCC compared to normal samples, which include two A-to-I editing events in the seed regions of hsa-mir-376a-3p and hsa-mir-376c-3p, respectively, and one C-to-U editing event in the seed region of hsa-mir-29c-3p. After comparing the targets of the original and edited miRNAs, we found that hsa-mir-376a-1_49g, hsa-mir-376c_48g and hsa-mir-29c_59u had many new targets, respectively. Many of these new targets were deregulated in ccRCC, which might be related to the different editing levels of hsa-mir-376a-3p, hsa-mir-376c-3p, hsa-mir-29c-3p in ccRCC compared to normal controls. Our study sheds new light on miRNA editing events and their potential biological functions in ccRCC.

摘要

透明细胞肾细胞癌(ccRCC)是一种起源于肾小管上皮的恶性肿瘤。虽然 ccRCC 的 microRNAs(miRNAs)转录组已经得到了广泛的研究,但 miRNA 编辑在 ccRCC 中的作用在很大程度上是未知的。通过分析 154 例 ccRCC 患者和 22 例正常对照的肾组织小 RNA 测序谱,我们从 246 个前体 miRNA 中鉴定出 1025 个 miRNA 编辑位点。与正常样本相比,ccRCC 中有 122 个编辑事件的编辑水平存在显著差异,其中包括 hsa-mir-376a-3p 和 hsa-mir-376c-3p 种子区的两个 A-to-I 编辑事件,以及 hsa-mir-29c-3p 种子区的一个 C-to-U 编辑事件。在比较原始和编辑 miRNA 的靶标后,我们发现 hsa-mir-376a-1_49g、hsa-mir-376c_48g 和 hsa-mir-29c_59u 分别具有许多新的靶标。这些新的靶标中的许多在 ccRCC 中被下调,这可能与 hsa-mir-376a-3p、hsa-mir-376c-3p、hsa-mir-29c-3p 在 ccRCC 中的编辑水平与正常对照相比存在差异有关。我们的研究为 miRNA 编辑事件及其在 ccRCC 中的潜在生物学功能提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e1/10499803/108de52c5790/41598_2023_42302_Fig1_HTML.jpg

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