Analysis of the Expression of PRDX6 in Patients with Hepatocellular Carcinoma and its Effect on the Phenotype of Hepatocellular Carcinoma Cells

Runhong Mu; Mingzhu Chang; Chuanbo Feng; Yunhe Cui; Tingyu Li; Chang Liu; Yilin Wang; Xiao Guo

doi:10.2174/0113892029273682240111052317

Analysis of the Expression of PRDX6 in Patients with Hepatocellular Carcinoma and its Effect on the Phenotype of Hepatocellular Carcinoma Cells

Curr Genomics. 2024 Feb 23;25(1):2-11. doi: 10.2174/0113892029273682240111052317.

Authors

Runhong Mu¹, Mingzhu Chang¹, Chuanbo Feng², Yunhe Cui¹, Tingyu Li¹, Chang Liu², Yilin Wang^{3

4}, Xiao Guo²

Affiliations

¹ Basic Medicine College of Beihua University, Jilin, 132000, P.R. China.
² School of Pharmacy, Beihua University, Jilin, 132000, P.R. China.
³ Zhuhai Integrated Traditional Chinese and Western Medicine Hospital, Zhuhai, 519000, China.
⁴ Zhuhai Hospital Affiliated to Southern Medical University, Zhuhai, 519000, China.

PMID: 38544826
PMCID: PMC10964084 (available on 2024-08-23)
DOI: 10.2174/0113892029273682240111052317

Abstract

Objectives: This research aimed to study the expression of PRDX6 mRNA in hepatocellular carcinoma (HCC) and its effect on the prognosis of HCC. Moreover, the effect of PRDX6 gene knockdown on the proliferation, migration, and invasion of HepG2 cells mediated by lentivirus was also examined. This study offers a theoretical and experimental basis for further research on the mechanism of PRDX6 in liver cancer and new methods for clinical diagnosis and treatment.

Methods: RNA sequence data of 369 HCC patients were screened through the TCGA database, and the expression and clinical characteristics of PRDX6 mRNA were analyzed based on high-throughput RNA sequencing data. HepG2 cells were divided into WT, sh-NC and sh-PRDX6 groups. Real-time PCR and Western blot were used to detect the expression levels of the PRDX6 gene and protein, respectively. CCK8 method was used to detect the proliferation activity of HepG2 cells, scratch healing test was used to detect the migration ability, Transwell chamber was used to detect the invasion ability, and Western blot was used to detect the expression levels of PI3K/Akt/mTOR signaling pathway and Notch signaling pathway-related proteins.

Results: The expression of PRDX6 was significantly correlated with the gender, race, clinical stage, histological grade, and survival time of HCC patients (P < 0.05). Compared with that in WT and sh-NC groups, the expression level of PRDX6 protein in HCC patients was significantly lower (P < 0.01), the proliferation activity of HCC cells was significantly decreased (P < 0.05), and the migration and invasion ability was significantly decreased (P < 0.05) in the sh-PRDX6 group. The expression levels of PI3K, p-Akt, p-mTOR, Notch1, and Hes1 proteins in the sh-PRDX6 group were significantly lower than those in WT and sh-NC groups (P < 0.05).

Conclusion: The expression of PRDX6 may be closely related to the prognosis of HCC. Lentivirus-mediated PRDX6 knockdown can inhibit the proliferation, migration and invasion of HCC cells, which may be related to its regulating the PI3K/Akt/mTOR and Notch1 signaling pathways. PRDX6 is expected to be a new target for the diagnosis and treatment of liver cancer.

Keywords: Hepatocellular carcinoma (HCC); RNA sequence data; gene knockdown; lentivirus; peroxiredoxin 6 (PRDX6); phenotype.