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鉴定PAFAH1B3作为肝细胞癌的候选预后标志物和潜在治疗靶点

Identification of PAFAH1B3 as Candidate Prognosis Marker and Potential Therapeutic Target for Hepatocellular Carcinoma.

作者信息

Xu Weikang, Lu Xinyu, Liu Jing, Chen Qianhui, Huang Xuan, Huang Kuiyuan, Liu Hongyan, Zhu Wei, Zhang Xiaoyong

机构信息

State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Department of Hematology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.

出版信息

Front Oncol. 2021 Aug 19;11:700700. doi: 10.3389/fonc.2021.700700. eCollection 2021.

Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer-related deaths worldwide. PAFAH1B3 plays an important role on occurrence and development in a variety tumor. However, the function of PAFAH1B3 in HCC remains unclear.

METHODS

The TIMER, ONCOMINE, Human Protein Atlas (HPA), GEPIA, The Cancer Genome Atlas (TCGA), HCCDB, UALCAN and LinkedOmics database were used to analyze the prognostic value, co-expression genes and regulator networks of PAFAH1B3 in HCC. siRNA transfections and inhibitor of PAFAH1B3 P11 were used to verify the anti-tumor effect on HCC cell lines. Gene expression was detected by qRT-PCR. The functions of PAFAH1B3 downregulation in HCC cell lines were investigated using cell cycle analysis, apoptosis detection, CCK8 assay and transwell assay. Western blot was used to evaluate the role of PAFAH1B3 on metabolic pathways in HCC cells.

RESULTS

Based on the data from databases, the expression of PAFAH1B3 was remarkably increased in HCC patients. High expression of PAFAH1B3 was associated with poorer overall survival (OS) and disease-free survival (DFS). And PAFAH1B3 was notably linked to age, sex, grade, stage, race, and TP53 mutational status. Then, the functional network analysis showed PAFAH1B3 may be involved in HCC through cell cycle, cell metabolism, spliceosome, and RNA transport. Furthermore, the mRNA expression of PAFAH1B3 was also increased in HCC cell lines. Flow cytometry analysis showed that PAFAH1B3 manipulated apoptosis and cell cycle regulation. CCK8 assay showed that PAFAH1B3 silencing or pharmacologic inhibitor of PAFAH1B3 inhibited the proliferation of HepG2, Huh7 and MHCC-97H cells. Transwell assay results showed that PAFAH1B3 silencing also significantly impaired the invasion and migratory ability of HCC cells. In addition, PAFAH1B3 silencing significantly downregulated the expression of glycolysis and lipid synthesis signaling pathways.

CONCLUSION

Our findings suggested that PAFAH1B3 plays a critical role in progression of HCC. PAFAH1B3 as a prognosis marker and potential target for HCC has prospective clinical significance.

摘要

背景

肝细胞癌(HCC)是全球癌症相关死亡的第四大主要原因。PAFAH1B3在多种肿瘤的发生和发展中起重要作用。然而,PAFAH1B3在HCC中的功能仍不清楚。

方法

使用TIMER、ONCOMINE、人类蛋白质图谱(HPA)、GEPIA、癌症基因组图谱(TCGA)、HCCDB、UALCAN和LinkedOmics数据库分析PAFAH1B3在HCC中的预后价值、共表达基因和调控网络。使用PAFAH1B3 P11的siRNA转染和抑制剂来验证对HCC细胞系的抗肿瘤作用。通过qRT-PCR检测基因表达。使用细胞周期分析、凋亡检测、CCK8测定和transwell测定研究PAFAH1B3下调在HCC细胞系中的功能。蛋白质免疫印迹法用于评估PAFAH1B3在HCC细胞代谢途径中的作用。

结果

基于数据库数据,HCC患者中PAFAH1B3的表达显著增加。PAFAH1B3的高表达与较差的总生存期(OS)和无病生存期(DFS)相关。并且PAFAH1B3与年龄、性别、分级、分期、种族和TP53突变状态显著相关。然后,功能网络分析表明PAFAH1B3可能通过细胞周期、细胞代谢、剪接体和RNA转运参与HCC。此外,PAFAH1B3在HCC细胞系中的mRNA表达也增加。流式细胞术分析表明PAFAH1B3调控凋亡和细胞周期。CCK8测定表明PAFAH1B3沉默或PAFAH1B3的药理抑制剂抑制HepG2、Huh7和MHCC-97H细胞的增殖。Transwell测定结果表明PAFAH1B3沉默也显著损害HCC细胞的侵袭和迁移能力此外,PAFAH1B3沉默显著下调糖酵解和脂质合成信号通路的表达。

结论

我们的研究结果表明PAFAH1B3在HCC进展中起关键作用。PAFAH1B3作为HCC的预后标志物和潜在靶点具有前瞻性临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd96/8418329/d0485c07508a/fonc-11-700700-g001.jpg

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