ST6Gal-I predicts postoperative clinical outcome for patients with localized clear-cell renal cell carcinoma

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Abstract

Hyperactivated a2-6-sialylation on N-glycans due to overexpression of the Golgi enzyme β-galactoside: a2-6-sialyltransferase (ST6Gal-I) often correlates with cancer progression, metastasis, and poor prognosis. This study was aimed to determine the association between ST6Gal-I expression and the risk of recurrence and survival of patients with localized clear-cell renal cell carcinoma (ccRCC) following surgery. We retrospectively enrolled 391 patients (265 in training cohort and 126 in validation cohort) with localized ccRCC underwent nephrectomy at a single center. Tissue microarrays were constructed for immunostaining of ST6Gal-I. Prognostic value and clinical outcomes were evaluated. High ST6Gal-I expression was associated with Fuhrman grade (p < 0.001 and p=0.016, respectively) and the University of California Los-Angeles Integrated Staging System (UISS) score (p=0.004 and p=0.017, respectively) in both cohorts. Patients with high ST6Gal-I expression had significantly worse overall survival (OS) (p < 0.001 and p < 0.001, respectively) and recurrence free survival (RFS) (p < 0.001 and p=0.002, respectively) than those with low expression in both cohorts. On multivariate analysis, ST6Gal-I expression remained associated with OS and RFS even after adjusting for the UISS score. Stratified analysis suggested that the association is more pronounced among patients with low and intermediate-risk disease defined by the UISS score. High ST6Gal-I expression is a potential independent adverse predictor of survival and recurrence in ccRCC patients, and the prognostic value is most prominent in those with low and intermediate-risk disease defined by the UISS score.

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APA

Liu, H. O., Wu, Q., Liu, W. S., Liu, Y. D., Fu, Q., Zhang, W. J., … Xu, J. J. (2014). ST6Gal-I predicts postoperative clinical outcome for patients with localized clear-cell renal cell carcinoma. Asian Pacific Journal of Cancer Prevention, 15(23), 10217–10223. https://doi.org/10.7314/APJCP.2014.15.23.10217

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