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Comprehensive Analysis of Anoikis-related Genes in Prognosis and Immune Infiltration of Gastric Cancer Based on Bulk and Single-cell RNA Sequencing Data

Overview
Specialty Oncology
Date 2023 Jul 20
PMID 37474682
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Abstract

Background: Accumulating evidence suggests that anoikis resistance is a key process in cancer cell metastasis, making it an attractive therapeutic target. Therefore, anoikis may become a new treatment for gastric cancer.

Methods: We used the univariate Cox regression method to screen gastric cancer-related anoikis genes, and a prognostic risk model was established. We analyzed differences between high- and low-risk groups in terms of tumor infiltrating immune cells, gene mutation signatures, and treatment of gastric cancer. Analysis of model associated genes at single-cell resolution was performed.

Results: We filtered to 12 anoikis-related genes and built a prognostic risk model using seven of them, which performed well in multiple datasets. Patients with CCDC178 mutations had a worse prognosis. We also found that patients at low risk were more likely to benefit from chemotherapy and immunotherapy. ERBB2 was found to be highly expressed in epithelial cells and fibroblasts. Our analysis also indicated that gastric cancer samples with high infiltration of iCAFs had a worse prognosis.

Conclusion: Seven anoikis-related genes were selected to establish a risk model. The model can be used to predict the prognosis of patients and guide the drug treatment, which provides a new idea for the evaluation and treatment of gastric cancer patients.

Citing Articles

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Anoikis-related genes as potential prognostic biomarkers in gastric cancer: A multilevel integrative analysis and predictive therapeutic value.

Lin Y, Liu J IET Syst Biol. 2024; 18(2):41-54.

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References
1.
Dias Amoedo N, Rodrigues M, Rumjanek F . Mitochondria: are mitochondria accessory to metastasis?. Int J Biochem Cell Biol. 2014; 51:53-7. DOI: 10.1016/j.biocel.2014.03.009. View

2.
Bray F, Ferlay J, Soerjomataram I, Siegel R, Torre L, Jemal A . Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018; 68(6):394-424. DOI: 10.3322/caac.21492. View

3.
Carvalho B, Irizarry R . A framework for oligonucleotide microarray preprocessing. Bioinformatics. 2010; 26(19):2363-7. PMC: 2944196. DOI: 10.1093/bioinformatics/btq431. View

4.
Chen Z, Li Y, Tan B, Zhao Q, Fan L, Li F . Progress and current status of molecule-targeted therapy and drug resistance in gastric cancer. Drugs Today (Barc). 2020; 56(7):469-482. DOI: 10.1358/dot.2020.56.7.3112071. View

5.
Chia N, Deng N, Das K, Huang D, Hu L, Zhu Y . Regulatory crosstalk between lineage-survival oncogenes KLF5, GATA4 and GATA6 cooperatively promotes gastric cancer development. Gut. 2014; 64(5):707-19. DOI: 10.1136/gutjnl-2013-306596. View