Identification of differentially expressed genomic repeats in primary hepatocellular carcinoma and their potential links to biological processes and survival.

Turkish journal of biology = Turk biyoloji dergisi Pub Date : 2021-10-18 eCollection Date: 2021-01-01 DOI:10.3906/biy-2104-13
Gökhan Karakülah, Cihangir Yandim
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引用次数: 1

Abstract

Hepatocellular carcinoma (HCC) is one of the deadliest cancers. Research on HCC so far primarily focused on genes and provided limited information on genomic repeats, which constitute more than half of the human genome and contribute to genomic stability. In line with this, repeat dysregulation was significantly shown to be pathological in various cancers and other diseases. In this study, we aimed to determine the full repeat expression profile of HCC for the first time. We utilised two independent RNA-seq datasets obtained from primary HCC tumours with matched normal tissues of 20 and 17 HCC patients, respectively. We quantified repeat expressions and analysed their differential expression. We also identified repeats that are cooperatively expressed with genes by constructing a gene coexpression network. Our results indicated that HCC tumours in both datasets harbour 24 differentially expressed repeats and even more elements were coexpressed with genes involved in various metabolic pathways. We discovered that two L1 elements (L1M3b, L1M3de) were downregulated and a handful of HERV subfamily repeats (HERV-Fc1-int, HERV3-int, HERVE_a-int, HERVK11D-int, HERVK14C-int, HERVL18-int) were upregulated with the exception of HERV1_LTRc, which was downregulated. Various LTR elements (LTR32, LTR9, LTR4, LTR52-int, LTR70) and MER elements (MER11C, MER11D, MER57C1, MER9a1, MER74C) were implicated along with few other subtypes including Charlie12, MLT2A2, Tigger15a, Tigger 17b. The only satellite repeat differentially expressed in both datasets was GSATII, whose expression was upregulated in 33 (>90%) out of 37 patients. Notably, GSATII expression correlated with HCC survival genes. Elements discovered here promise future studies to be considered for biomarker and HCC therapy research. The coexpression pattern of the GSATII satellite with HCC survival genes and the fact that it has been upregulated in the vast majority of patients make this repeat particularly stand out for HCC.

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原发性肝细胞癌中差异表达基因组重复序列的鉴定及其与生物学过程和生存的潜在联系。
肝细胞癌(HCC)是最致命的癌症之一。迄今为止,对HCC的研究主要集中在基因上,并提供了有限的基因组重复序列信息,这些重复序列占人类基因组的一半以上,有助于基因组的稳定性。与此相一致的是,重复基因失调在各种癌症和其他疾病中都是病理性的。在这项研究中,我们旨在首次确定HCC的完整重复表达谱。我们使用了两个独立的RNA-seq数据集,分别从20例和17例HCC患者的原发HCC肿瘤和匹配的正常组织中获得。我们量化重复表达并分析其差异表达。我们还通过构建基因共表达网络,确定了与基因协同表达的重复序列。我们的研究结果表明,两个数据集中的HCC肿瘤含有24个差异表达的重复序列,甚至更多的元件与参与各种代谢途径的基因共表达。我们发现两个L1元素(L1M3b, L1M3de)下调,少数HERV亚家族重复序列(HERV- fc1 -int, HERV3-int, HERVE_a-int, HERVK11D-int, HERVK14C-int, HERVL18-int)上调,但HERV1_LTRc下调。各种LTR元件(LTR32、LTR9、LTR4、LTR52-int、LTR70)和MER元件(MER11C、MER11D、MER57C1、MER9a1、MER74C)与Charlie12、MLT2A2、Tigger15a、tigger17b等其他亚型都有关联。两个数据集中唯一的卫星重复序列差异表达是GSATII,在37例患者中有33例(>90%)表达上调。值得注意的是,GSATII的表达与HCC存活基因相关。在此发现的元素有望在未来的生物标志物和HCC治疗研究中得到考虑。GSATII卫星与HCC存活基因的共表达模式,以及它在绝大多数患者中被上调的事实,使得这种重复在HCC中尤为突出。
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