2. Academic Validation
  3. Arginine methylation of HSPA8 by PRMT9 inhibits ferroptosis to accelerate hepatitis B virus-associated hepatocellular carcinoma progression

Arginine methylation of HSPA8 by PRMT9 inhibits ferroptosis to accelerate hepatitis B virus-associated hepatocellular carcinoma progression

  • J Transl Med. 2023 Sep 15;21(1):625. doi: 10.1186/s12967-023-04408-9.
Wensheng Deng # 1,  Jiaoyu Ai # 2,  Wanlin Zhang # 3,  Zhenyu Zhou 4,  Muqi Li 1,  Likun Yan 1,  Lidong Zhang 1,  Zongjing Huang 1,  Ziyi Wu 1,  Junhua Ai 5,  Hai Jiang 6
Affiliations

Affiliations

  • 1 Department of General Surgery, The First Affiliated Hospital of Nanchang University, No. 17 Yongwaizheng Street, Donghu District, Nanchang City, 330000, Jiangxi, China.
  • 2 Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, 330000, Jiangxi, China.
  • 3 Department of Clinical Laboratory, Ningbo Yinzhou No. 2 Hospital Ningbo Urology and Nephtology Hospital, Ningbo, 315100, Zhejiang, China.
  • 4 Department of Hepatobiliary Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, 510120, China.
  • 5 Department of General Surgery, The First Affiliated Hospital of Nanchang University, No. 17 Yongwaizheng Street, Donghu District, Nanchang City, 330000, Jiangxi, China. [email protected].
  • 6 Department of General Surgery, The First Affiliated Hospital of Nanchang University, No. 17 Yongwaizheng Street, Donghu District, Nanchang City, 330000, Jiangxi, China. [email protected].
  • # Contributed equally.
PMID: 37715221 DOI: 10.1186/s12967-023-04408-9
Abstract

Background: The hepatitis B virus X (HBx) protein is an established cause of hepatitis B virus (HBV)-induced hepatocellular carcinoma (HCC). Whether arginine methylation regulates Ferroptosis involved in HBx-induced HCC progression has not been reported. This study aimed to explore whether HBx-regulated protein arginine methyltransferase 9 (PRMT9) mediates the involvement of Ferroptosis in the development of HCC.

Methods and results: HBx inhibited Ferroptosis through promoting PRMT9 expression in HCC cells. PRMT9 suppressed Ferroptosis to accelerate HCC progression in vivo. PRMT9 targeted HSPA8 and enhanced arginine methylation of HSPA8 at R76 and R100 to regulate Ferroptosis in HCC. HSPA8 overexpression altered the transcriptome profile of HepG2 cells, in particular, Ferroptosis and immune-related pathways were significantly enriched by differentially expressed genes, including CD44. HSPA8 overexpression up-regulated CD44 expression and knockdown of CD44 significantly reversed the inhibition of Ferroptosis caused by PRMT9 overexpression.

Conclusions: In conclusion, HBx/PRMT9/HSPA8/CD44 axis is a vital signal pathway regulating Ferroptosis in HCC cells. This study provides new opportunities and targets for the treatment of HBV-induced HCC.

Keywords

Arginine methylation; CD44; Ferroptosis; HSPA8; Hepatitis B virus X; Hepatocellular carcinoma; PRMT9.

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