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Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer

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- si...

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Autores principales: Ko, Chou-Yuan, Chu, Tian-Huei, Hsu, Ching-Cheng, Chen, Hsin-Pao, Huang, Shih-Chung, Chang, Chen-Lin, Tzou, Shiow-Jyu, Chen, Tung-Yuan, Lin, Chia-Chen, Shih, Pei-Chun, Lin, Chung-Hsien, Chang, Chuan-Fa, Lee, Yung-Kuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953768/
https://www.ncbi.nlm.nih.gov/pubmed/35330401
http://dx.doi.org/10.3390/jpm12030401
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author Ko, Chou-Yuan
Chu, Tian-Huei
Hsu, Ching-Cheng
Chen, Hsin-Pao
Huang, Shih-Chung
Chang, Chen-Lin
Tzou, Shiow-Jyu
Chen, Tung-Yuan
Lin, Chia-Chen
Shih, Pei-Chun
Lin, Chung-Hsien
Chang, Chuan-Fa
Lee, Yung-Kuo
author_facet Ko, Chou-Yuan
Chu, Tian-Huei
Hsu, Ching-Cheng
Chen, Hsin-Pao
Huang, Shih-Chung
Chang, Chen-Lin
Tzou, Shiow-Jyu
Chen, Tung-Yuan
Lin, Chia-Chen
Shih, Pei-Chun
Lin, Chung-Hsien
Chang, Chuan-Fa
Lee, Yung-Kuo
author_sort Ko, Chou-Yuan
collection PubMed
description 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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spelling pubmed-89537682022-03-26 Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer Ko, Chou-Yuan Chu, Tian-Huei Hsu, Ching-Cheng Chen, Hsin-Pao Huang, Shih-Chung Chang, Chen-Lin Tzou, Shiow-Jyu Chen, Tung-Yuan Lin, Chia-Chen Shih, Pei-Chun Lin, Chung-Hsien Chang, Chuan-Fa Lee, Yung-Kuo J Pers Med Article 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. MDPI 2022-03-04 /pmc/articles/PMC8953768/ /pubmed/35330401 http://dx.doi.org/10.3390/jpm12030401 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ko, Chou-Yuan
Chu, Tian-Huei
Hsu, Ching-Cheng
Chen, Hsin-Pao
Huang, Shih-Chung
Chang, Chen-Lin
Tzou, Shiow-Jyu
Chen, Tung-Yuan
Lin, Chia-Chen
Shih, Pei-Chun
Lin, Chung-Hsien
Chang, Chuan-Fa
Lee, Yung-Kuo
Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title_full Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title_fullStr Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title_full_unstemmed Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title_short Bioinformatics Analyses Identify the Therapeutic Potential of ST8SIA6 for Colon Cancer
title_sort bioinformatics analyses identify the therapeutic potential of st8sia6 for colon cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953768/
https://www.ncbi.nlm.nih.gov/pubmed/35330401
http://dx.doi.org/10.3390/jpm12030401
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