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
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Kaohsiung Armed Forces General Hospital, Kaohsiung 80284, Taiwan.
Institute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
J Pers Med. 2022 Mar 4;12(3):401. doi: 10.3390/jpm12030401.
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.
糖蛋白的唾液酸化由不同的唾液酸转移酶修饰,如ST3Gal、ST6Gal、ST6GalNAc或ST8SIA,它们形成α2,3-、α2,6-或α2,8-连接。这些唾液酸转移酶的改变导致异常唾液酸化,与结肠癌的进展相关。然而,在ST8-唾液酸转移酶中,ST8SIA6在结肠癌中的作用仍知之甚少。在本研究中,我们使用多个基因数据库探索了ST8SIA6在结肠癌中的作用。通过UALCAN分析研究了ST8SIA6表达与肿瘤分期/分级之间的关系,并使用Kaplan-Meier Plotter分析来分析ST8SIA6表达对结肠癌患者生存结果的影响。此外,使用LinkedOmics和癌细胞代谢基因数据库探索了ST8SIA6在结肠癌中的生物学功能。最后,分别使用TIMER和TISMO分析来描述ST8SIA6在肿瘤免疫和免疫治疗反应中的水平。ST8SIA6下调与晚期和低分化分级相关;然而,ST8SIA6表达并不影响结肠癌患者的生存结果。基因本体分析表明,ST8SIA6参与细胞表面黏附、血管生成和膜泡运输。此外,ST8SIA6水平影响结肠癌中的免疫细胞浸润和免疫治疗反应。总的来说,这些结果表明,ST8SIA6可能作为结肠癌个性化医学的一个新的治疗靶点。