CDC123 promotes Hepatocellular Carcinoma malignant progression by regulating CDKAL1

被引:1
作者
Wang, Yong [1 ]
Pan, Hongtao [1 ]
Gong, Xuankun [1 ,2 ]
Wang, Zhicheng [1 ,2 ]
Qin, Xiliang [1 ,2 ]
Zhou, Shuai [1 ]
Zhu, Chao [1 ]
Hu, Xiaosi [1 ]
Chen, Shilei [1 ]
Liu, Huichun [1 ]
Jin, Hao [1 ]
Pang, Qing [1 ,2 ]
Wu, WenYong [1 ,2 ]
机构
[1] Anhui Med Univ, Anhui Prov Peoples Hosp 2, Clin Coll, Hefei 230041, Anhui, Peoples R China
[2] Bengbu Med Coll, Dept Oncol Surg, Affiliated Hosp 1, Bengbu 233004, Anhui, Peoples R China
关键词
Hepatocellular Carcinoma; TCGA; CDC123; Proliferation and Apoptosis; CDKAL1; GENOME-WIDE ASSOCIATION; GENETIC-VARIANTS; PROTEIN; CANCER; INHIBITION; EXPRESSION; CHINESE; MUTANT; CYCLE; RISK;
D O I
10.1016/j.prp.2023.154987
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The cell proliferation protein 123 (CDC123) is involved in the synthesis of the eukaryotic initiation factor 2 (eIF2), which regulates eukaryotic translation. Although CDC123 is considered a candidate oncogene in breast cancer, its expression and role in Hepatocellular Carcinoma (HCC) remain unknown. Herein, we obtained the CDC123 RNA-seq and clinical prognostic data from the TCGA database. The mRNA level revealed that CDC123 was highly expressed in HCC patients, and Kaplan -Meier analysis implied better prognoses in HCC patients with low CDC123 expression (P < 0.001). The multivariate Cox analysis revealed that the CDC123 level was an independent prognostic factor (P < 0.001). We further confirmed a high CDC123 expression in HCC cell lines. Additionally, we found that CDC123 knockdown in HCC cell lines significantly inhibited cellular proliferation, invasion, and migration. Moreover, CDC123 was co -expressed with the CDK5 Regulatory Subunit -Associated Protein 1 Like 1 (CDKAL1), whose mRNA level was decreased after silencing CDC123. Therefore, we hypothesized that CDC123 promotes HCC progression by regulating CDKAL1.
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页数:11
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