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A Transcriptomic Analysis of Cancer-Stromal Interactome in Lung Cancer Xenograft Models
Yuriko Takayama-Isagawa1, Daisuke Komura2, Takayuki Isagawa3
1Division of Tumor Pathology, Department of Pathology, Jichi Medical University, Shimotsuke, Japan.
Cancer Science
|December 11, 2025
Summary
This study reveals key ligand-receptor pairs driving lung adenocarcinoma aggressiveness. Tumor necrosis factor superfamily member 12/receptor superfamily member 12A signaling is identified as a potential therapeutic target for this cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Cancer-stromal interactions are crucial in lung adenocarcinoma progression.
- Identifying specific molecular players in these interactions is essential for understanding tumor aggressiveness.
Purpose of the Study:
- To comprehensively analyze the lung cancer interactome.
- To identify key ligand-receptor pairs involved in lung adenocarcinoma aggressiveness.
- To evaluate the prognostic value of identified factors.
Main Methods:
- Transcriptome data from lung cancer cell line xenografts were analyzed.
- Cancer-stromal interactome analysis was performed in both directions.
- Prognostic value was assessed using multiple public datasets and immunohistochemistry.
Main Results:
- 1150 cancer-stromal interactions were identified, with 117 selected based on intensity.
- 21 prognostic ligand-receptor pairs were identified.
- Tumor necrosis factor superfamily member 12 (TNFSF12) and its receptor, tumor necrosis factor receptor superfamily member 12A (TNFRSF12A), were highlighted.
Conclusions:
- TNFSF12/TNFRSF12A signaling axis contributes to lung adenocarcinoma aggressiveness.
- TNFRSF12A expression correlates with tumor size, invasion, and stage in clinical specimens.
- This signaling axis represents a potential therapeutic target for lung adenocarcinoma.
Keywords:
cell to cell interactionimmunohistochemistrylung adenocarcinomatumor microenvironmentxenograft
