Natural bioactive compounds and STAT3 against hepatocellular carcinoma: An update

Life Sci. 2024 Jan 15:337:122351. doi: 10.1016/j.lfs.2023.122351. Epub 2023 Dec 15.

Abstract

Hepatocellular carcinoma (HCC) is a challenging and very fatal liver cancer. The signal transducer and activator of transcription 3 (STAT3) pathway is a crucial regulator of tumor development and are ubiquitously active in HCC. Therefore, targeting STAT3 has emerged as a promising approach for preventing and treating HCC. Various natural bioactive compounds (NBCs) have been proven to target STAT3 and have the potential to prevent and treat HCC as STAT3 inhibitors. Numerous kinds of STAT3 inhibitors have been identified, including small molecule inhibitors, peptide inhibitors, and oligonucleotide inhibitors. Due to the undesirable side effects of the conventional therapeutic drugs against HCC, the focus is shifted to NBCs derived from plants and other natural sources. NBCs can be broadly classified into the categories of terpenes, alkaloids, carotenoids, and phenols. Most of the compounds belong to the family of terpenes, which prevent tumorigenesis by inhibiting STAT3 nuclear translocation. Further, through STAT3 inhibition, terpenes downregulate matrix metalloprotease 2 (MMP2), matrix metalloprotease 9 (MMP9) and vascular endothelial growth factor (VEGF), modulating metastasis. Terpenes also suppress the anti-apoptotic proteins and cell cycle markers. This review provides comprehensive information related to STAT3 abrogation by NBCs in HCC with in vitro and in vivo evidences.

Keywords: Hepatocellular carcinoma; Natural bioactive compounds; STAT3 inhibitors; STAT3 signaling; Terpenes.

Publication types

  • Review

MeSH terms

  • Carcinoma, Hepatocellular* / pathology
  • Cell Line, Tumor
  • Cell Proliferation
  • Humans
  • Liver Neoplasms* / pathology
  • Metalloproteases / metabolism
  • STAT3 Transcription Factor / metabolism
  • Terpenes / pharmacology
  • Terpenes / therapeutic use
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • STAT3 Transcription Factor
  • Vascular Endothelial Growth Factor A
  • Terpenes
  • Metalloproteases
  • STAT3 protein, human