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Beta-1,4-galactosyltransferase II predicts poor prognosis of patients with non-metastatic clear-cell renal cell carcinoma

Authors :
Haijian Zhang
Yidong Liu
Huyang Xie
Qiang Fu
Zheng Liu
Yu Zhu
Le Xu
Weijuan Zhang
Yuanfeng Yang
Jiejie Xu
Source :
Tumor Biology, Vol 39 (2017)
Publication Year :
2017
Publisher :
IOS Press, 2017.

Abstract

Beta-1,4-galactosyltransferase II is found to be associated with the alterations of tumor-related glycosylation. However, the clinical significance of beta-1,4-galactosyltransferase II in non-metastatic clear-cell renal cell carcinoma has not been reported up to now. Herein, our researches suggested that the expression level of beta-1,4-galactosyltransferase II was first found to be positively associated with tumor size, Fuhrman grade, lymphovascular invasion, rhabdoid differentiation, tumor necrosis and poor overall survival and recurrence-free survival of patients with non-metastatic clear-cell renal cell carcinoma, both in training set and validation set. Moreover, beta-1,4-galactosyltransferase II expression was identified as an independent adverse prognosticator for overall survival and recurrence-free survival of patients with non-metastatic clear-cell renal cell carcinoma. Ultimately, prognostic accuracy of the nomogram integrating beta-1,4-galactosyltransferase II with other independent prognostic parameters was dramatically improved for overall survival and recurrence-free survival of patients with non-metastatic clear-cell renal cell carcinoma. Taken together, beta-1,4-galactosyltransferase II is a potential independent adverse prognostic factor for postoperative recurrence and survival, which could be developed as a useful biomarker for non-metastatic clear-cell renal cell carcinoma by a series of further independent and retrospective studies, so as to help the postsurgical management of clear-cell renal cell carcinoma patients.

Details

Language :
English
ISSN :
14230380 and 10104283
Volume :
39
Database :
Directory of Open Access Journals
Journal :
Tumor Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.518f3ee8fe04079804f1b297bedb858
Document Type :
article
Full Text :
https://doi.org/10.1177/1010428317691417