Department of Ophthalmology, Yidu Central Hospital of Weifang, Qingzhou, People's Republic of China.
Department of Hepatobiliary and Vascular Surgery, Yidu Central Hospital of Weifang, Qingzhou, People's Republic of China.
Cancer Biother Radiopharm. 2019 Dec;34(10):626-633. doi: 10.1089/cbr.2019.2778. Epub 2019 Oct 17.
AHNAK nucleoprotein 2 (AHNAK2) is supposed to participate in calcium signaling and cytoarchitecture by directly interacting with some proteins. Recently, it was identified as a novel candidate oncogene in human tumors. The author's present study aimed to investigate the expression and biological function of AHNAK2 in uveal melanoma (UM). Based on microarray data of 63 UM patients that were downloaded from Gene Expression Omnibus database, the authors found that AHNAK2 expression is higher in UM primary tumor tissues from patients who developed metastases after enucleation than that in UM primary tumor tissues from patients without metastasis after enucleation. On the basis of the data obtained from The Cancer Genome Atlas database, they found that high AHNAK2 expression is closely associated with shorter overall survival time in UM patients. From quantitative reverse transcription polymerase chain reaction analyses, they revealed that the mRNA expression level of AHNAK2 was significantly upregulated in M17 and SP6.5 cell lines compared with that in D78. Functionally, knockdown of AHNAK2 using small interfering RNA in M17 and SP6.5 cells dramatically suppressed cell proliferation, migratory and invasive abilities, as well as inhibited the activation of phosphatidylinositol 3-kinase (PI3K) signaling pathway. Taken together, their results illustrated that AHNAK2 was upregulated in UM and plays a promoting role in the proliferation and migration of UM cells possibly via regulating PI3K signaling pathway.
AHNAK 核蛋白 2(AHNAK2)通过直接与某些蛋白质相互作用,被认为参与钙信号转导和细胞结构。最近,它被鉴定为人类肿瘤中的一种新的候选癌基因。作者目前的研究旨在研究 AHNAK2 在葡萄膜黑色素瘤(UM)中的表达和生物学功能。作者根据从基因表达综合数据库下载的 63 名 UM 患者的微阵列数据,发现从行眼球摘除法后发生转移的 UM 患者原发性肿瘤组织中 AHNAK2 的表达高于从行眼球摘除法后无转移的 UM 患者原发性肿瘤组织中的表达。基于从癌症基因组图谱数据库获得的数据,他们发现高 AHNAK2 表达与 UM 患者的总生存时间较短密切相关。通过定量逆转录聚合酶链反应分析,他们揭示了 M17 和 SP6.5 细胞系中 AHNAK2 的 mRNA 表达水平明显高于 D78。功能上,在 M17 和 SP6.5 细胞中使用小干扰 RNA 敲低 AHNAK2 显著抑制了细胞增殖、迁移和侵袭能力,并抑制了磷酸肌醇 3-激酶(PI3K)信号通路的激活。总之,他们的结果表明,AHNAK2 在 UM 中上调,并通过调节 PI3K 信号通路在 UM 细胞的增殖和迁移中发挥促进作用。