Neoprzewaquinone A Inhibits Breast Cancer Cell Migration and Promotes Smooth Muscle Relaxation by Targeting PIM1 to Block ROCK2/STAT3 Pathway

Int J Mol Sci. 2023 Mar 13;24(6):5464. doi: 10.3390/ijms24065464.

Abstract

Salvia miltiorrhiza Bunge (Danshen) has been widely used to treat cancer and cardiovascular diseases in Chinese traditional medicine. Here, we found that Neoprzewaquinone A (NEO), an active component of S. miltiorrhiza, selectively inhibits PIM1. We showed that NEO potently inhibits PIM1 kinase at nanomolar concentrations and significantly suppresses the growth, migration, and Epithelial-Mesenchymal Transition (EMT) in the triple-negative breast cancer cell line, MDA-MB-231 in vitro. Molecular docking simulations revealed that NEO enters the PIM1 pocket, thereby triggering multiple interaction effects. Western blot analysis revealed that both NEO and SGI-1776 (a specific PIM1 inhibitor), inhibited ROCK2/STAT3 signaling in MDA-MB-231 cells, indicating that PIM1 kinase modulates cell migration and EMT via ROCK2 signaling. Recent studies indicated that ROCK2 plays a key role in smooth muscle contraction, and that ROCK2 inhibitors effectively control the symptoms of high intraocular pressure (IOP) in glaucoma patients. Here, we showed that NEO and SGI-1776 significantly reduce IOP in normal rabbits and relax pre-restrained thoracic aortic rings in rats. Taken together, our findings indicated that NEO inhibits TNBC cell migration and relaxes smooth muscles mainly by targeting PIM1 and inhibiting ROCK2/STAT3 signaling, and that PIM1 may be an effective target for IOP and other circulatory diseases.

Keywords: Neoprzewaquinone A; PIM1; ROCK2/STAT3 signaling pathway; TNBC; cell migration; glaucoma.

MeSH terms

  • Animals
  • Cardiovascular Diseases*
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Epithelial-Mesenchymal Transition
  • Humans
  • Molecular Docking Simulation
  • Muscle Relaxation
  • Proto-Oncogene Proteins c-pim-1 / metabolism
  • Rabbits
  • Rats
  • STAT3 Transcription Factor / metabolism
  • Triple Negative Breast Neoplasms* / drug therapy
  • Triple Negative Breast Neoplasms* / metabolism
  • rho-Associated Kinases / metabolism

Substances

  • neoprzewaquinone A
  • PIM1 protein, human
  • Proto-Oncogene Proteins c-pim-1
  • STAT3 protein, human
  • STAT3 Transcription Factor
  • ROCK2 protein, human
  • rho-Associated Kinases
  • ROCK2 protein, rat

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