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日本肺腺癌患者核糖体 RNA 基因启动子区域中频繁的种系和体细胞单核苷酸变异。

Frequent Germline and Somatic Single Nucleotide Variants in the Promoter Region of the Ribosomal RNA Gene in Japanese Lung Adenocarcinoma Patients.

机构信息

Histopathology Core Facility, Niigata University Faculty of Medicine, Niigata 951-8510, Japan.

Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.

出版信息

Cells. 2020 Nov 3;9(11):2409. doi: 10.3390/cells9112409.

Abstract

Ribosomal RNA (rRNA), the most abundant non-coding RNA species, is a major component of the ribosome. Impaired ribosome biogenesis causes the dysfunction of protein synthesis and diseases called "ribosomopathies," including genetic disorders with cancer risk. However, the potential role of rRNA gene (rDNA) alterations in cancer is unknown. We investigated germline and somatic single-nucleotide variants (SNVs) in the rDNA promoter region (positions -248 to +100, relative to the transcription start site) in 82 lung adenocarcinomas (LUAC). Twenty-nine tumors (35.4%) carried germline SNVs, and eight tumors (9.8%) harbored somatic SNVs. Interestingly, the presence of germline SNVs between positions +1 and +100 ( = 12; 14.6%) was associated with significantly shorter recurrence-free survival (RFS) and overall survival (OS) by univariate analysis ( < 0.05, respectively), and was an independent prognostic factor for RFS and OS by multivariate analysis. LUAC cell line PC9, carrying rDNA promoter SNV at position +49, showed significantly higher ribosome biogenesis than H1650 cells without SNV. Upon nucleolar stress induced by actinomycin D, PC9 retained significantly higher ribosome biogenesis than H1650. These results highlight the possible functional role of SNVs at specific sites of the rDNA promoter region in ribosome biogenesis, the progression of LUAC, and their potential prognostic value.

摘要

核糖体 RNA(rRNA)是最丰富的非编码 RNA 种类,是核糖体的主要组成部分。核糖体生物发生受损会导致蛋白质合成功能障碍,并引发“核糖体病”,包括具有癌症风险的遗传疾病。然而,rRNA 基因(rDNA)改变在癌症中的潜在作用尚不清楚。我们研究了 82 例肺腺癌(LUAC)中 rDNA 启动子区域(相对于转录起始位点为-248 到+100 位)的种系和体细胞单核苷酸变异(SNVs)。29 个肿瘤(35.4%)携带种系 SNVs,8 个肿瘤(9.8%)携带体细胞 SNVs。有趣的是,位于+1 到+100 位(=12;14.6%)的种系 SNVs 的存在与单因素分析中明显较短的无复发生存(RFS)和总生存(OS)相关(<0.05),并且是多因素分析中 RFS 和 OS 的独立预后因素。携带 rDNA 启动子 SNV 位于+49 位的 LUAC 细胞系 PC9 比没有 SNV 的 H1650 细胞显示出明显更高的核糖体生物发生。在 Actinomycin D 诱导核仁应激时,PC9 比 H1650 保留了明显更高的核糖体生物发生。这些结果突出了 rDNA 启动子区域特定位点 SNVs 在核糖体生物发生、LUAC 进展及其潜在预后价值中的可能功能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0706/7692307/f16f8d837962/cells-09-02409-g001.jpg

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