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Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
Published on: September 15, 2023
Association Between Phosphorylated AXL Expression and Survival in Patients with Gastric Cancer
Hua Ho1, Chiao-Yin Cheng2, Chun-Yen Huang1,2
1Department of Emergency Medicine, Far Eastern Memorial Hospital, New Taipei 220, Taiwan.
Higher expression of phosphorylated AXL (pAXL) in gastric cancer patients correlates with better survival, especially in males. This finding suggests pAXL may be a valuable prognostic marker and potential therapeutic target for gastric cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Gastric cancer (GC) remains a significant cause of cancer mortality, particularly in East Asia, due to late diagnosis and metastasis.
- Phosphorylated AXL (pAXL), a receptor tyrosine kinase, is implicated in promoting cancer progression, epithelial-mesenchymal transition (EMT), and metastasis.
Purpose of the Study:
- To investigate the association between pAXL expression and prognosis in gastric cancer (GC) patients.
- To evaluate pAXL as a prognostic marker alongside fibronectin and phosphorylated AKT (pAkt).
Main Methods:
- Immunohistochemistry was used to assess pAXL, fibronectin, and pAkt expression in 188 GC specimens.
- Kaplan-Meier survival analysis and multivariate logistic regression were employed to analyze the association between pAXL expression and patient outcomes.
Main Results:
- Higher pAXL expression was significantly linked to improved survival rates, notably in male GC patients.
- pAXL expression positively correlated with fibronectin and pAkt upregulation, indicating a role in tumor invasion and EMT.
- pAXL, fibronectin, and pAkt were identified as significant prognostic indicators in multivariate analysis.
Conclusions:
- pAXL serves as a valuable prognostic marker in GC, with higher levels correlating to better survival, particularly in males.
- pAXL appears to enhance GC cell invasiveness via fibronectin and pAkt, positioning it as a potential therapeutic target.
- Further research into pAXL-targeted therapies is warranted to understand their role in GC progression and treatment.
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