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本文引用的文献

1
Synthetic essentiality of chromatin remodelling factor CHD1 in PTEN-deficient cancer.染色质重塑因子CHD1在PTEN缺陷型癌症中的合成必需性
Nature. 2017 Feb 23;542(7642):484-488. doi: 10.1038/nature21357. Epub 2017 Feb 6.
2
PI3K/AKT/mTOR: role in breast cancer progression, drug resistance, and treatment.PI3K/AKT/mTOR:在乳腺癌进展、耐药性和治疗中的作用。
Cancer Metastasis Rev. 2016 Dec;35(4):515-524. doi: 10.1007/s10555-016-9637-x.
3
Acquired savolitinib resistance in non-small cell lung cancer arises via multiple mechanisms that converge on MET-independent mTOR and MYC activation.非小细胞肺癌中获得性赛沃替尼耐药通过多种机制产生,这些机制汇聚于不依赖MET的mTOR和MYC激活。
Oncotarget. 2016 Sep 6;7(36):57651-57670. doi: 10.18632/oncotarget.10859.
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Genetic polymorphisms of mTOR and cancer risk: a systematic review and updated meta-analysis.mTOR的基因多态性与癌症风险:系统评价与更新的荟萃分析。
Oncotarget. 2016 Aug 30;7(35):57464-57480. doi: 10.18632/oncotarget.10805.
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Precursors of tRNAs are stabilized by methylguanosine cap structures.tRNA 的前体通过甲基鸟苷帽结构稳定。
Nat Chem Biol. 2016 Aug;12(8):648-55. doi: 10.1038/nchembio.2117. Epub 2016 Jun 27.
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SHOT-RNAs: A novel class of tRNA-derived functional RNAs expressed in hormone-dependent cancers.SHOT-RNAs:一类在激素依赖性癌症中表达的新型tRNA衍生功能性RNA。
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7
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9
tDRmapper: challenges and solutions to mapping, naming, and quantifying tRNA-derived RNAs from human small RNA-sequencing data.tDRmapper:从人类小RNA测序数据中对tRNA衍生RNA进行映射、命名和定量的挑战与解决方案
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Sex hormone-dependent tRNA halves enhance cell proliferation in breast and prostate cancers.性激素依赖性的tRNA半体可增强乳腺癌和前列腺癌中的细胞增殖。
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tsRNA 特征与癌症。

tsRNA signatures in cancer.

机构信息

Department of Cancer Biology and Medical Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210.

Department of Biochemistry, University of Vermont College of Medicine, Burlington, VT 05405.

出版信息

Proc Natl Acad Sci U S A. 2017 Jul 25;114(30):8071-8076. doi: 10.1073/pnas.1706908114. Epub 2017 Jul 10.

DOI:10.1073/pnas.1706908114
PMID:28696308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5544330/
Abstract

Small, noncoding RNAs are short untranslated RNA molecules, some of which have been associated with cancer development. Recently we showed that a class of small RNAs generated during the maturation process of tRNAs (tRNA-derived small RNAs, hereafter "tsRNAs") is dysregulated in cancer. Specifically, we uncovered tsRNA signatures in chronic lymphocytic leukemia and lung cancer and demonstrated that the cluster (now called "" and "," respectively), , and are down-regulated in these malignancies. Furthermore, we showed that tsRNAs are similar to Piwi-interacting RNAs (piRNAs) and demonstrated that and can associate with PiwiL2, a protein involved in the silencing of transposons. In this study, we extended our investigation on tsRNA signatures to samples collected from patients with colon, breast, or ovarian cancer and cell lines harboring specific oncogenic mutations and representing different stages of cancer progression. We detected tsRNA signatures in all patient samples and determined that tsRNA expression is altered upon oncogene activation and during cancer staging. In addition, we generated a knocked-out cell model for and in HEK-293 cells and found significant differences in gene-expression patterns, with activation of genes involved in cell survival and down-regulation of genes involved in apoptosis and chromatin structure. Finally, we overexpressed and in two lung cancer cell lines and performed a clonogenic assay to examine their role in cell proliferation. We observed a strong inhibition of colony formation in cells overexpressing these tsRNAs compared with untreated cells, confirming that tsRNAs affect cell growth and survival.

摘要

小非编码 RNA 是短的非翻译 RNA 分子,其中一些与癌症的发展有关。最近,我们表明,在 tRNA 成熟过程中产生的一类小 RNA(tRNA 衍生的小 RNA,以下简称“tsRNAs”)在癌症中失调。具体来说,我们在慢性淋巴细胞白血病和肺癌中发现了 tsRNA 特征,并证明了簇(现在分别称为“”和“”)、、和在这些恶性肿瘤中下调。此外,我们表明 tsRNAs 类似于 Piwi 相互作用 RNA(piRNAs),并表明和可以与 PiwiL2 结合,PiwiL2 是一种参与转座子沉默的蛋白质。在这项研究中,我们将 tsRNA 特征的研究扩展到来自结肠癌、乳腺癌或卵巢癌患者以及携带特定致癌突变并代表癌症进展不同阶段的细胞系的样本。我们在所有患者样本中都检测到了 tsRNA 特征,并确定 tsRNA 表达在致癌基因激活和癌症分期过程中发生改变。此外,我们在 HEK-293 细胞中生成了用于和的敲除细胞模型,并发现基因表达模式存在显著差异,涉及细胞存活的基因被激活,而涉及细胞凋亡和染色质结构的基因被下调。最后,我们在两种肺癌细胞系中过表达和,并进行集落形成实验以检查它们在细胞增殖中的作用。与未处理的细胞相比,过表达这些 tsRNAs 的细胞中集落形成明显受到抑制,证实了 tsRNAs 影响细胞生长和存活。