β-elemene promotes miR-127-3p maturation, induces NSCLCs autophagy, and enhances macrophage M1 polarization through

Xiahui Wu1,2, Jie Wu3, Tingting Dai4

  • 1Department of Oncology, Lianyungang Integrated Traditional Chinese and Western Medicine Clinical College, Nanjing University of Chinese Medicine, Nanjing, 222002, China.

PubMed

Insights

Beta-elemene inhibits non-small cell lung cancer (NSCLC) by inducing autophagy and promoting macrophage M1 polarization. This study reveals beta-elemene

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Beta-elemene exhibits anti-tumor properties across various cancers.
  • Non-small cell lung cancer (NSCLC) remains a significant health challenge.
  • Understanding beta-elemene's mechanisms in NSCLC is crucial for therapeutic development.

Purpose of the Study:

  • To investigate the role and molecular mechanisms of beta-elemene in non-small cell lung cancer (NSCLC).
  • To elucidate how beta-elemene influences cancer cell autophagy and the tumor microenvironment.

Main Methods:

  • In vitro and in vivo experimental models of NSCLC.
  • Analysis of microRNA (miR-127-3p) maturation and exosomal packaging.
  • Investigation of signaling pathways including Akt/mTOR/p70S6K and macrophage polarization.

Main Results:

  • Beta-elemene inhibits NSCLC proliferation and induces apoptosis.
  • Beta-elemene promotes miR-127-3p maturation by inhibiting CBX8, leading to autophagy induction via the MAPK4/Akt/mTOR/p70S6K pathway.
  • Beta-elemene enhances exosomal miR-127-3p packaging, which promotes M1 macrophage polarization by suppressing ZC3H4.

Conclusions:

  • Beta-elemene effectively inhibits NSCLC through intricate molecular pathways.
  • The study highlights beta-elemene's dual action in inducing cancer cell autophagy and modulating immune responses.
  • Beta-elemene shows significant potential as a therapeutic agent for NSCLC.