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The Establishment of a Lung Colonization Assay for Circulating Tumor Cell Visualization in Lung Tissues
Published on: June 16, 2018
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.
Abstract:
Non-Small Cell Lung Cancer (NSCLC) remains a leading cause of cancer-related deaths worldwide, creating an urgent need to explore new drugs and clarify their mechanisms of action. In recent years, lactic acid bacteria-derived extracellular vesicles (EVs) have shown great potential in anti-tumor therapy; however, research on their role in lung cancer remains limited. In this study, EVs from three common Lactobacillus species were isolated to verify their anti-tumor effects on lung cancer. Among these, the extracellular vesicles derived from Lactobacillus rhamnosus GG (LGG-EVs) exhibited the most significant anti-cancer activity. A549 and H1299 cells were treated with LGG-EVs, and transcriptome sequencing analysis was performed. The results revealed that Alcohol Dehydrogenase Iron-Containing 1 (ADHFE1)- a differentially expressed gene with notable changes before and after treatment- displayed the same expression pattern in both cell lines. Further verification was conducted using methods including Western Blotting, Transwell, wound healing, and flow cytometry. Compared with the control group, treatment with LGG-EVs led to downregulated ADHFE1 expression in both cell lines, along with inhibited malignant cellular behaviors and glycolysis capacity. Notably, overexpression of ADHFE1 significantly reversed these effects. These findings indicate that the anti-tumor effect of LGG-EVs on lung cancer may be achieved through ADHFE1-mediated metabolic reprogramming. This study is the first to identify that ADHFE1-mediated metabolic reprogramming could be a key mechanism by which LGG-EVs inhibit lung cancer, providing a new target and strategy for lung cancer treatment.
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.