Koufaris Costas, Kirmizis Antonis
Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
Front Oncol. 2021 Jun 2;11:691950. doi: 10.3389/fonc.2021.691950. eCollection 2021.
Liver hepatocellular carcinoma (LIHC) is a leading cause of cancer-related mortality. In this study we initially interrogated the Cancer Genome Atlas (TCGA) dataset to determine the implication of N-terminal acetyltransferases (NATs), a family of enzymes that modify the N-terminus of the majority of eukaryotic proteins, in LIHC. This examination unveiled NAA40 as the NAT family member with the most prominent upregulation and significant disease prognosis for this cancer. Focusing on this enzyme, which selectively targets histone proteins, we show that its upregulation occurs from early stages of LIHC and is not specifically correlated with any established risk factors such as viral infection, obesity or alcoholic disease. Notably, in silico analysis of TCGA and other LIHC datasets found that expression of this epigenetic enzyme is associated with high proliferating, poorly differentiating and more aggressive LIHC subtypes. In particular, NAA40 upregulation was preferentially linked to mutational or non-mutational P53 functional inactivation. Accordingly, we observed that high NAA40 expression was associated with worse survival specifically in liver cancer patients with inactivated P53. These findings define NAA40 as a NAT with potentially oncogenic functions in LIHC and uncover its prognostic value for aggressive LIHC subtypes.
肝细胞癌(LIHC)是癌症相关死亡的主要原因。在本研究中,我们最初对癌症基因组图谱(TCGA)数据集进行分析,以确定N-末端乙酰转移酶(NATs)(一类修饰大多数真核蛋白质N-末端的酶)在LIHC中的作用。这项研究表明,NAA40是NAT家族成员中上调最为显著的,且对该癌症具有显著的疾病预后价值。聚焦于这种选择性靶向组蛋白的酶,我们发现其上调在LIHC早期阶段就已出现,且与病毒感染、肥胖或酒精性疾病等任何既定风险因素均无特异性关联。值得注意的是,对TCGA和其他LIHC数据集的计算机分析发现,这种表观遗传酶的表达与高增殖、低分化和更具侵袭性的LIHC亚型相关。特别是,NAA40上调优先与P53的突变或非突变功能失活相关。因此,我们观察到,高NAA40表达尤其在P53失活的肝癌患者中与较差的生存率相关。这些发现将NAA40定义为一种在LIHC中具有潜在致癌功能的NAT,并揭示了其对侵袭性LIHC亚型的预后价值。