1. Academic Validation
  2. Circ_0008043 promotes the metastasis of hepatocellular carcinoma by regulating the miR-661/PLEKHG4B axis

Circ_0008043 promotes the metastasis of hepatocellular carcinoma by regulating the miR-661/PLEKHG4B axis

  • Sci Rep. 2025 Jul 8;15(1):24580. doi: 10.1038/s41598-025-10618-6.
Kangjun Zhang 1 Taishi Fang 2 Qijun Chen 2 Xu Yan 2 Xin Jin 2 Nan Ma 2
Affiliations

Affiliations

  • 1 Department of Liver Surgery and Transplantation, Transplant Center, The Third People's Hospital of Shenzhen (The Second Affiliated Hospital of Southern University of Science and Technology), No. 29 Bulan Road, Longgang District, Shenzhen, 518000, Guangdong Province, China. zkangjunhk@126.com.
  • 2 Department of Liver Surgery and Transplantation, Transplant Center, The Third People's Hospital of Shenzhen (The Second Affiliated Hospital of Southern University of Science and Technology), No. 29 Bulan Road, Longgang District, Shenzhen, 518000, Guangdong Province, China.
Abstract

Circular RNAs (circRNAs) play a critical role in hepatocellular carcinoma (HCC) progression. Although circ_0008043 is predicted to be highly expressed in HCC tissues, its functional role and molecular mechanisms remain poorly understood. In this study, we investigated the effects of circ_0008043 on HCC metastasis and its regulation of the miR-661/PLEKHG4B axis. Functional assays revealed that circ_0008043 knockdown suppressed HCC cell viability, migration, and epithelial-mesenchymal transition (EMT). Mechanistically, circ_0008043 acted as a Sponge for miR-661, which directly targeted PLEKHG4B. Rescue experiments demonstrated that miR-661 inhibition or PLEKHG4B overexpression counteracted the effects of circ_0008043 silencing or miR-661 overexpression. Furthermore, we identified ESRP1 as a key regulator promoting circ_0008043 biogenesis. In vivo experiments confirmed that circ_0008043 knockdown significantly inhibited lung metastasis. Collectively, our findings reveal that ESRP1-derived circ_0008043 facilitates HCC cell migration and EMT by modulating the miR-661/PLEKHG4B axis, thereby promoting tumor metastasis. This study provides novel insights into the molecular mechanisms of HCC progression and suggests a potential therapeutic target for HCC treatment.

Keywords

Circ_0008043; Hepatocellular carcinoma; Migration; PLEKHG4B; miR-661.

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