The cytoplasmic expression of FSTL3 correlates with colorectal cancer progression, metastasis status and prognosis.
Chien-Hsiu LiChih-Yeu FangMing-Hsien ChanChi-Long ChenMichael HsiaoMichael HsiaoPublished in: Journal of cellular and molecular medicine (2023)
Follistatin-like (FSTL) family members are associated with cancer progression. However, differences between FSTL members with identical cancer types have not been systematically investigated. Among the most malignant tumours worldwide, colorectal cancer (CRC) has high metastatic potential and chemoresistance, which makes it challenging to treat. A systematic examination of the relationship between the expression of FSTL family members in CRC will provide valuable information for prognosis and therapeutic development. Based on large cohort survival analyses, we determined that FSTL3 was associated with a significantly worse prognosis in CRC at the RNA and protein levels. Immunohistochemistry staining of CRC specimens revealed that FSTL3 expression levels in the cytosol were significantly associated with a poor prognosis in terms of overall and disease-free survival. Molecular simulation analysis showed that FSTL3 participated in multiple cell motility signalling pathways via the TGF-β1/TWIST1 axis to control CRC metastasis. The findings provide evidence of the significance of FSTL3 in the oncogenesis and metastasis of CRC. FSTL3 may be useful as a diagnostic or prognostic biomarker, and as a potential therapeutic target.
Keyphrases
- poor prognosis
- long non coding rna
- free survival
- papillary thyroid
- small cell lung cancer
- squamous cell carcinoma
- squamous cell
- pseudomonas aeruginosa
- epithelial mesenchymal transition
- healthcare
- binding protein
- risk assessment
- escherichia coli
- transforming growth factor
- human health
- biofilm formation
- high resolution
- atomic force microscopy
- childhood cancer