Red fermented rice elution fractions inhibits cancer cell proliferation by regulating the FGFR1/PI3K/AKT signaling pathway

Fitoterapia. 2024 Sep:177:106079. doi: 10.1016/j.fitote.2024.106079. Epub 2024 Jun 17.

Abstract

This study aims to elucidate the potential targets and molecular mechanisms underlying the anticancer effects of Red fermented rice extract using molecular simulation techniques. The inhibitory effects of different elution fractions of Red fermented rice extract on A549 and MCF-7 cell proliferation were evaluated through CCK-8 assays. Liquid chromatography-mass spectrometry (LC-MS) was employed to elucidate the structural information of active components, while molecular simulation techniques aided in identifying target proteins based on small molecule structures. Protein immunoblotting was utilized to investigate the mechanisms of action of relevant targets. The study found that the petroleum ether-ethyl acetate and ethyl acetate elution fractions of Red fermented rice extract significantly inhibited A549 and MCF-7 cell proliferation, with stronger effects observed on A549 cells. LC-MS structural analysis identified 25 small molecule structures. Molecular simulations successfully revealed interaction between active elution fractions of Red fermented rice extract and the cancer-related protein FGFR1. Further investigation into the phosphorylation of FGFR1 and its downstream pathway targets PI3K/AKT demonstrated that the active elution fractions exerted their anticancer activity by inhibiting the phosphorylation of FGFR1, PI3K, and AKT proteins. This comprehensive study, integrating CCK-8 assays, LC-MS, molecular simulation techniques, and protein immunoblotting, provides a deep understanding of the anticancer mechanisms of Red fermented rice extract, guiding its further development and clinical application.

Keywords: Anticancer effects; Liquid chromatography-mass spectrometry; Molecular simulation techniques; Potential targets; Protein immunoblotting; Red fermented rice extract.

MeSH terms

  • A549 Cells
  • Antineoplastic Agents, Phytogenic / isolation & purification
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Proliferation* / drug effects
  • Fermentation*
  • Humans
  • MCF-7 Cells
  • Molecular Structure
  • Oryza* / chemistry
  • Phosphatidylinositol 3-Kinases* / metabolism
  • Phosphorylation
  • Plant Extracts* / chemistry
  • Plant Extracts* / pharmacology
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Receptor, Fibroblast Growth Factor, Type 1* / metabolism
  • Signal Transduction* / drug effects

Substances

  • Proto-Oncogene Proteins c-akt
  • Phosphatidylinositol 3-Kinases
  • Plant Extracts
  • Receptor, Fibroblast Growth Factor, Type 1
  • FGFR1 protein, human
  • Antineoplastic Agents, Phytogenic