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Updated: Jul 2, 2025

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Studying the Effects of Tumor-Secreted Paracrine Ligands on Macrophage Activation using Co-Culture with Permeable Membrane Supports
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Predictable regulation of survival by intratumoral microbe-immune crosstalk in patients with lung adenocarcinoma
Shuo Shi1, Yuwen Chu2,3, Haiyan Liu4,5
1The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China.
Microbial Cell (Graz, Austria)
|February 20, 2024
Summary
Intratumoral microbes influence lung adenocarcinoma (LUAD) prognosis by affecting the tumor immune microenvironment (TIME). Differences in microbial communities correlate with patient survival risk, suggesting new therapeutic targets.
Area of Science:
- Oncology
- Microbiology
- Immunology
Background:
- Intratumoral microbiota modulate the tumor immune microenvironment (TIME), impacting cancer prognosis.
- The role of intratumoral microbes in lung adenocarcinoma (LUAD) progression and TIME is under investigation.
Purpose of the Study:
- To investigate the association between intratumoral microbial communities and prognosis in LUAD.
- To explore the relationship between intratumoral microbiota, immune cells, and patient survival outcomes in LUAD.
Main Methods:
- Utilized The Cancer Genome Atlas (TCGA) database for LUAD patients (n=478).
- Analyzed matched tumor microbiome, host transcriptome, and survival data.
- Employed machine learning models based on immune cell marker genes for survival prediction and risk stratification.
Main Results:
- Machine learning models accurately predicted 1- to 5-year survival in LUAD patients.
- Significant differences in intratumoral microbial communities were observed between high- and low-survival-risk groups.
- High-risk patients exhibited higher alpha diversity and enrichment of *Streptococcus*, while low-risk patients showed more active microbial-immune crosstalk.
Conclusions:
- Intratumoral microbiota-immune crosstalk is strongly associated with LUAD prognosis.
- Findings suggest intratumoral microbes and their interaction with the immune system as potential targets for precise therapeutic strategies in LUAD.
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