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