Clinical diagnostic value of PIMREG on liver cancer cell phenotype and tumorigenic ability in nude mice.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.62347/YVEE7827
Lei Zhang, Kaiyun Peng, Aijun Gao
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引用次数: 0

Abstract

Objectives: In vitro experiments were manipulated to investigate the effect of the PIMREG (PICALM-interacting mitotic regulator gene) expression level on the malignant phenotype of liver cancer cells and their tumorigenesis ability in nude mice, and bioinformatics were used to analyze the clinical diagnostic and prognostic value in liver cancer.

Methods: After liver cancer-related data were obtained from the TCGA database and GTEx database, the differences in PIMREG expression in liver cancer and normal liver tissue were compared using bioinformatics, and their correlation with the clinical pathological characteristics of liver cancer and the prognosis value were analyzed. A knockdown and overexpression model of PIMREG was constructed using Huh7 cells. The effect of the PIMREG expression level on the malignant phenotype of Huh7 cells was tested through CCK-8 and Transwell experiments. At the same time, animal knockdown and overexpression models were constructed to study the effect of the PIMREG expression level on the tumorigenesis ability in nude mice.

Results: Bioinformatics analysis showed that PIMREG mRNA was significantly overexpressed in liver cancer tissue (P<0.001). There were differences in T-staging (P<0.001), pathological staging (P=0.002), vascular infiltration (P<0.001), histological grading (P<0.001), and AFP levels (P<0.001) between the high- and low-expression groups. A high expression of PIMREG is associated with a poor prognosis, manifested as a significant decrease in the overall survival, disease-specific survival, and progression-free survival rates of patients (P values of 0.006, 0.014, and 0.002, respectively). In the PIMREG overexpression model, the proliferation rate and invasion ability of Huh7 cells were significantly increased, and the tumorigenesis ability of nude mice was significantly enhanced. In the knockdown model, the opposite results were observed.

Conclusions: The PIMREG gene is highly expressed in hepatocellular carcinoma, and increasing its expression level can significantly promote the malignant phenotype of liver cancer cells and their tumorigenesis ability in nude mice. Knocking down its expression level has the opposite effect. The expression level of PIMREG is related to the pathological stages of liver cancer patients, and its elevated expression is a risk factor for poor prognosis. PIMREG may become a new target for the clinical diagnosis, treatment, and prognosis evaluation of liver cancer.

PIMREG对裸鼠肝癌细胞表型及致瘤能力的临床诊断价值。
目的:通过体外实验研究picalm互作有丝分裂调节基因(PIMREG)表达水平对裸鼠肝癌细胞恶性表型及成瘤能力的影响,并应用生物信息学方法分析其对肝癌的临床诊断和预后价值。方法:从TCGA数据库和GTEx数据库获取肝癌相关数据后,利用生物信息学方法比较PIMREG在肝癌和正常肝组织中的表达差异,并分析其与肝癌临床病理特征的相关性及预后价值。利用Huh7细胞构建PIMREG敲低过表达模型。通过CCK-8和Transwell实验检测PIMREG表达水平对Huh7细胞恶性表型的影响。同时,构建动物敲低和过表达模型,研究PIMREG表达水平对裸鼠肿瘤发生能力的影响。结果:生物信息学分析显示,PIMREG mRNA在肝癌组织中显著过表达(PPP=0.002),血管浸润(PPPPIMREG)与预后不良相关,表现为患者总生存率、疾病特异性生存率和无进展生存率显著降低(P值分别为0.006、0.014和0.002)。在PIMREG过表达模型中,Huh7细胞的增殖率和侵袭能力明显提高,裸鼠的成瘤能力明显增强。在knockdown模型中,观察到相反的结果。结论:PIMREG基因在肝细胞癌中高表达,提高其表达水平可显著促进裸鼠肝癌细胞的恶性表型及成瘤能力。降低其表达水平会产生相反的效果。PIMREG的表达水平与肝癌患者的病理分期有关,其表达升高是肝癌患者预后不良的危险因素。PIMREG可能成为肝癌临床诊断、治疗及预后评价的新靶点。
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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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552
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