Graduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan.
Sci Rep. 2017 Jun 30;7(1):4466. doi: 10.1038/s41598-017-04732-3.
Carbonic anhydrase IX (CA9) expression level has been considered as a poor prognostic factor in hepatocellular carcinoma (HCC) patients. However, the judging criteria of CA9 level is hard to define for potential clinical applications. Unlike CA9 expression level, CA9 polymorphism is poorly documented in HCC. Here, we found that people carry A allele at CA9 rs1048638, a 3'UTR SNP, has higher risk of HCC. rs1048638-CA correlates with advanced stages, larger tumor sizes, more vascular invasion, and shorter survival of HCC patients. A allele at CA9 rs1048638 impairs miR-34a, a tumor suppressor miRNA in HCC, binding to CA9 3'UTR and desensitizes CA9 mRNA to miR-34a-dependent RNA degradation. CA9 expression levels were also correlated with miR-34a levels and rs1048638 genotypes in HCC patients. rs1048638 influences HCC risk and progression through effects on miR-34a-targeted CA9 expression in HCC. In conclusion, genetic variations of the CA9 3'UTR play important roles in regulating CA9 expression and cancer progression, which is a novel determinant and target for HCC metastasis and prognosis.
碳酸酐酶 9(CA9)表达水平被认为是肝细胞癌(HCC)患者预后不良的因素。然而,CA9 水平的判断标准很难定义其在潜在的临床应用中的价值。与 CA9 表达水平不同,CA9 多态性在 HCC 中记录较少。在这里,我们发现 CA9 rs1048638(一个 3'UTR SNP)的 A 等位基因携带者患 HCC 的风险更高。rs1048638-CA 与 HCC 患者的晚期、更大的肿瘤大小、更多的血管侵犯和更短的生存时间相关。CA9 rs1048638 上的 A 等位基因可损害 miR-34a,miR-34a 是 HCC 中的一种肿瘤抑制 miRNA,它与 CA9 3'UTR 结合并使 CA9 mRNA 对 miR-34a 依赖的 RNA 降解脱敏。CA9 表达水平也与 HCC 患者的 miR-34a 水平和 rs1048638 基因型相关。rs1048638 通过影响 miR-34a 靶向 CA9 表达来影响 HCC 的风险和进展。总之,CA9 3'UTR 的遗传变异在调节 CA9 表达和癌症进展中起着重要作用,这是 HCC 转移和预后的一个新的决定因素和靶点。