Extracellular vesicles derived from Lactobacillus rhamnosus GG inhibit lung cancer cell invasion and metastasis by

Yang Wang1, Shuai Shen2, Ni Chen2

  • 1Department of Thoracic Surgery, Yunnan Provincial Clinical Research Center for Respiratory System Diseases, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming 650034, China.

Insights

Lactic acid bacteria-derived extracellular vesicles (EVs) show anti-cancer effects in Non-Small Cell Lung Cancer (NSCLC). Lactobacillus rhamnosus GG-EVs inhibit cancer growth by downregulating ADHFE1, suggesting a new therapeutic strategy.

Area of Science:

  • Oncology
  • Microbiology
  • Biochemistry

Background:

  • Non-Small Cell Lung Cancer (NSCLC) is a major global health concern requiring novel therapeutic strategies.
  • Lactic acid bacteria-derived extracellular vesicles (EVs) show promise in anti-tumor therapy, but their role in lung cancer is under-explored.

Purpose of the Study:

  • To investigate the anti-tumor effects of Lactobacillus species-derived EVs on Non-Small Cell Lung Cancer (NSCLC) cells.
  • To elucidate the underlying molecular mechanisms, focusing on gene expression changes and metabolic reprogramming.

Main Methods:

  • Isolation of EVs from three Lactobacillus species and assessment of their anti-cancer activity.
  • Transcriptome sequencing, Western Blotting, Transwell assays, wound healing assays, and flow cytometry on NSCLC cell lines (A549, H1299) treated with LGG-EVs.
  • Gene silencing and overexpression studies to validate the role of ADHFE1.

Main Results:

  • Extracellular vesicles from Lactobacillus rhamnosus GG (LGG-EVs) demonstrated significant anti-cancer activity against NSCLC cells.
  • LGG-EV treatment downregulated Alcohol Dehydrogenase Iron-Containing 1 (ADHFE1) expression, inhibited malignant cellular behaviors, and reduced glycolysis.
  • Overexpression of ADHFE1 reversed the anti-tumor effects induced by LGG-EVs.

Conclusions:

  • LGG-EVs exert anti-tumor effects on Non-Small Cell Lung Cancer (NSCLC) by downregulating ADHFE1 expression.
  • ADHFE1-mediated metabolic reprogramming is identified as a key mechanism for LGG-EVs' anti-cancer activity in NSCLC.
  • LGG-EVs and ADHFE1 present a potential new therapeutic target and strategy for NSCLC treatment.