AHNAK2 Promotes the Progression of Differentiated Thyroid Cancer through PI3K/AKT Signaling Pathway.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Min Xu, Jialiang Wen, Qiding Xu, Huihui Li, Bangyi Lin, Adheesh Bhandari, Jinmiao Qu
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引用次数: 0

Abstract

Aims: AHNAK2 may be used as a candidate marker for TC diagnosis and treatment.

Background: Thyroid cancer (TC) is the most frequent malignancy in endocrine carcinoma, and the incidence has been increasing for decades.

Objective: To understand the molecular mechanism of DTC, we performed next-generation sequencing (NGS) on 79 paired DTC tissues and normal thyroid tissues. The RNA-sequencing (RNA-seq) data analysis results indicated that AHNAK nucleoprotein 2 (AHNAK2) was significantly upregulated in the thyroid cancer patient's tissue.

Methods: We also analyzed AHNAK2 mRNA levels of DTC tissues and normal tissues from The Cancer Genome Atlas (TCGA). The association between the expression level of AHNAK2 and clinicopathological features was evaluated in the TCGA cohort. Furthermore, AHNAK2 gene expression was analyzed by quantitative real-time polymerase chain reaction (qRT-PCR) in 40 paired DTC tissues and adjacent normal thyroid tissues. The receiver operating characteristic (ROC) curve was performed to evaluate the diagnostic value of AHNAK2. For cell experiments in vitro, AHNAK2 was knocked down using small interfering RNA (siRNA), and the biological function of AHNAK2 in TC cell lines was investigated. The expression of AHNAK2 was significantly upregulated in both the TCGA cohort and the local cohort.

Results: The analysis results of the TCGA cohort indicated that the upregulation of AHNAK2 was associated with tumor size (P < 0.001), lymph node metastasis (P < 0.001), and disease stage (P < 0.001). The area under the curve (AUC, TCGA: P < 0.0001; local validated cohort: P < 0.0001) in the ROC curve revealed that AHNAK2 might be considered a diagnostic biomarker for TC. The knockdown of AHNAK2 reduced TC cell proliferation, colony formation, migration, invasion, cell cycle, and induced cell apoptosis.

Conclusion: Furthermore, the protein levels of phospho-PI3 Kinase p85 and phospho-AKT were downregulated in the transfected TC cell. Our study results indicate that AHNAK2 may promote metastasis and proliferation of thyroid cancer through PI3K/AKT signaling pathway. Thus, AHNAK2 may be used as a candidate marker for TC diagnosis and treatment.

AHNAK2通过PI3K/AKT信号通路促进分化型甲状腺癌的进展
目的:AHNAK2可作为甲状腺癌诊断和治疗的候选标志物:背景:甲状腺癌(TC)是内分泌癌中最常见的恶性肿瘤,几十年来发病率一直呈上升趋势:为了了解 DTC 的分子机制,我们对 79 例成对的 DTC 组织和正常甲状腺组织进行了新一代测序(NGS)。RNA-sequencing(RNA-seq)数据分析结果表明,AHNAK核蛋白2(AHNAK2)在甲状腺癌患者组织中显著上调:我们还分析了DTC组织和癌症基因组图谱(TCGA)中正常组织的AHNAK2 mRNA水平。在TCGA队列中评估了AHNAK2表达水平与临床病理特征之间的关联。此外,还通过实时定量聚合酶链反应(qRT-PCR)分析了40个配对的DTC组织和邻近正常甲状腺组织中AHNAK2基因的表达情况。采用接收者操作特征曲线(ROC)评估AHNAK2的诊断价值。在体外细胞实验中,使用小干扰RNA(siRNA)敲除AHNAK2,并研究AHNAK2在TC细胞系中的生物学功能。在TCGA队列和本地队列中,AHNAK2的表达均明显上调:TCGA队列的分析结果表明,AHNAK2的上调与肿瘤大小(P < 0.001)、淋巴结转移(P < 0.001)和疾病分期(P < 0.001)有关。ROC曲线的曲线下面积(AUC,TCGA:P < 0.0001;本地验证队列:P < 0.0001)显示,AHNAK2可被视为TC的诊断生物标志物。AHNAK2的敲除可减少TC细胞的增殖、集落形成、迁移、侵袭、细胞周期,并诱导细胞凋亡:此外,转染的TC细胞中磷酸-PI3激酶p85和磷酸-AKT的蛋白水平下调。我们的研究结果表明,AHNAK2 可通过 PI3K/AKT 信号通路促进甲状腺癌的转移和增殖。因此,AHNAK2可作为TC诊断和治疗的候选标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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