Department of Hepatobiliary Surgery, The Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.
Oncology Department, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
J Int Med Res. 2020 Jul;48(7):300060520936879. doi: 10.1177/0300060520936879.
Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related deaths worldwide. This study investigated the relationship between cyclin-dependent kinase inhibitor (CDKN)3 and prognosis and pathological characteristics in HCC patients to determine whether it could be used as a prognostic factor and/or therapeutic target for HCC drug development.
We previously showed that CDKN3 is deregulated in HCC tumor samples. Here, bioinformatics analysis was used to assess the relationship between CDKN3 gene expression and the characteristics of HCC patients from Gene Expression Omnibus and The Cancer Genome Atlas databases. Additionally, CDKN3 expression was silenced by small interfering RNA to determine its effect on HCC cell proliferation and on HCC cell sensitivity to adriamycin chemotherapy.
Bioinformatics analysis showed a negative correlation between CDKN3 expression and both disease-free survival and overall survival. CDKN3 silencing did not significantly suppress the proliferation of HCC cells, but did decrease their sensitivity to adriamycin.
CDKN3 may have a dual role during the development of HCC, and could be used as an independent prognostic factor and therapeutic target for HCC treatment.
肝细胞癌(HCC)是全球癌症相关死亡的最常见原因之一。本研究探讨了细胞周期蛋白依赖性激酶抑制剂(CDKN)3 与 HCC 患者预后和病理特征之间的关系,以确定其是否可作为 HCC 药物开发的预后因素和/或治疗靶点。
我们之前表明 CDKN3 在 HCC 肿瘤样本中失调。在这里,我们使用生物信息学分析评估了来自基因表达综合数据库和癌症基因组图谱数据库的 CDKN3 基因表达与 HCC 患者特征之间的关系。此外,通过小干扰 RNA 沉默 CDKN3 表达,以确定其对 HCC 细胞增殖和 HCC 细胞对阿霉素化疗敏感性的影响。
生物信息学分析显示 CDKN3 表达与无病生存率和总生存率呈负相关。CDKN3 沉默并未显著抑制 HCC 细胞的增殖,但确实降低了它们对阿霉素的敏感性。
CDKN3 在 HCC 的发展过程中可能具有双重作用,可作为 HCC 治疗的独立预后因素和治疗靶点。