Journal of Personalized Medicine (Mar 2022)

Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer

  • Chou-Yuan Ko,
  • Tian-Huei Chu,
  • Ching-Cheng Hsu,
  • Hsin-Pao Chen,
  • Shih-Chung Huang,
  • Chen-Lin Chang,
  • Shiow-Jyu Tzou,
  • Tung-Yuan Chen,
  • Chia-Chen Lin,
  • Pei-Chun Shih,
  • Chung-Hsien Lin,
  • Chuan-Fa Chang,
  • Yung-Kuo Lee

DOI
https://doi.org/10.3390/jpm12030401
Journal volume & issue
Vol. 12, no. 3
p. 401

Abstract

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Sialylation of glycoproteins is modified by distinct sialyltransferases such as ST3Gal, ST6Gal, ST6GalNAc, or ST8SIA with α2,3-, α2,6-, or α2,8-linkages. Alteration of these sialyltransferases causing aberrant sialylation is associated with the progression of colon cancer. However, among the ST8- sialyltransferases, the role of ST8SIA6 in colon cancer remains poorly understood. In this study, we explored the involvement of ST8SIA6 in colon cancer using multiple gene databases. The relationship between ST8SIA6 expression and tumor stages/grades was investigated by UALCAN analysis, and Kaplan–Meier Plotter analysis was used to analyze the expression of ST8SIA6 on the survival outcome of colon cancer patients. Moreover, the biological functions of ST8SIA6 in colon cancer were explored using LinkedOmics and cancer cell metabolism gene DB. Finally, TIMER and TISMO analyses were used to delineate ST8SIA6 levels in tumor immunity and immunotherapy responses, respectively. ST8SIA6 downregulation was associated with an advanced stage and poorly differentiated grade; however, ST8SIA6 expression did not affect the survival outcomes in patients with colon cancer. Gene ontology analysis suggested that ST8SIA6 participates in cell surface adhesion, angiogenesis, and membrane vesicle trafficking. In addition, ST8SIA6 levels affected immunocyte infiltration and immunotherapy responses in colon cancer. Collectively, these results suggest that ST8SIA6 may serve as a novel therapeutic target towards personalized medicine for colon cancer.

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