Shang L, Jiang W, Zhang J, Wu W
Key Laboratory of Cancer Research and Clinical Laboratory Diagnosis, School of Laboratory Medicine, Bengbu Medical College, Bengbu 233030, China.
Department of Biochemistry and Molecular Biology, School of Laboratory Medicine, Bengbu Medical College, Bengbu 233030, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2022 May 20;42(5):665-672. doi: 10.12122/j.issn.1673-4254.2022.05.06.
To investigate the role of proline 4-hydroxylase Ⅱ (P4HA2) in the occurrence and progression of liver cancer.
GEPIA and Human Protein Atlas database were used to predict the expression of P4HA2 in hepatocellular carcinoma (HCC), and K-M plotter online database was used to analyze the relationship between P4HA2 expression and the prognosis of HCC. We also examined the expressions of P4HA2 in HCC cells and normal hepatocytes using qRT-PCR and Western blotting. With lentivirus-mediated RNA interference, P4HA2 expression was knocked down in hepatoma SNU-449 and Hep-3B cells, and the changes in cell proliferation, migration and invasion were assessed using cell counting kit-8 (CCK-8) assay, colony formation test, scratch test and Transwell assay. The changes in the expressions of epithelial-mesenchymal transition (EMT) and PI3K/Akt/mTOR signal pathway-related proteins were detected using Western blotting.
Online database analysis showed that the expression of P4HA2 was significantly higher in HCC tissues than in normal liver tissues ( < 0.05). The expression levels of P4HA2 mRNA and protein were also significantly higher in HCC cell lines than in normal hepatocytes ( < 0.01). Lentivirus-mediated RNA interference of P4HA2 significantly lowered the expression levels of P4HA2 mRNA and protein in the hepatoma cells ( < 0.05) and caused obvious inhibition of cell proliferation, migration and invasion. P4HA2 knockdown significantly increased the expression of E-cadherin protein, lowered the expressions of N-cadherin and Snail, and obviously decreased the expressions of phosphorylated PI3K, AKT and mTOR ( < 0.05).
P4HA2 enhances the proliferation, migration, invasion, and EMT of hepatoma cells by activating the PI3K/Akt/mTOR signaling pathway to promote the occurrence and progression of liver cancer.
探讨脯氨酸4-羟化酶Ⅱ(P4HA2)在肝癌发生发展中的作用。
利用GEPIA和人类蛋白质图谱数据库预测P4HA2在肝细胞癌(HCC)中的表达,使用K-M plotter在线数据库分析P4HA2表达与HCC预后的关系。我们还通过qRT-PCR和蛋白质印迹法检测了HCC细胞和正常肝细胞中P4HA2的表达。通过慢病毒介导的RNA干扰,在肝癌SNU-449和Hep-3B细胞中敲低P4HA2表达,并使用细胞计数试剂盒-8(CCK-8)检测、集落形成试验、划痕试验和Transwell试验评估细胞增殖、迁移和侵袭的变化。通过蛋白质印迹法检测上皮-间质转化(EMT)和PI3K/Akt/mTOR信号通路相关蛋白表达的变化。
在线数据库分析显示,HCC组织中P4HA2的表达明显高于正常肝组织(<0.05)。HCC细胞系中P4HA2 mRNA和蛋白质的表达水平也明显高于正常肝细胞(<0.01)。慢病毒介导的P4HA2 RNA干扰显著降低了肝癌细胞中P4HA2 mRNA和蛋白质的表达水平(<0.05),并明显抑制了细胞增殖、迁移和侵袭。敲低P4HA2显著增加了E-钙黏蛋白的表达,降低了N-钙黏蛋白和Snail的表达,并明显降低了磷酸化PI3K、AKT和mTOR的表达(<0.05)。
P4HA2通过激活PI3K/Akt/mTOR信号通路增强肝癌细胞的增殖、迁移、侵袭和EMT,从而促进肝癌的发生发展。