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High Transaldolase 1 expression predicts poor survival of patients with upper tract urothelial carcinoma.

Authors :
Wu YR
Lee YC
Li WM
Hsu WC
Lin HH
Chang LL
Huang AM
Jhan JH
Wu WJ
Li CC
Lee HY
Yeh HC
Ke HL
Source :
Pathology international [Pathol Int] 2021 Jul; Vol. 71 (7), pp. 463-470. Date of Electronic Publication: 2021 Apr 13.
Publication Year :
2021

Abstract

Upper tract urothelial carcinoma (UTUC) is a rare tumor with an incidence that varies greatly between Eastern and Western countries. Transaldolase 1 (TALDO1) is a rate-limiting enzyme of the pentose phosphate pathway. In humans, aberrant TALDO1 activity has been implicated in various autoimmune diseases and malignancies; however, the function of TALDO1 in UTUC has not been previously investigated. Here we evaluated the clinical significance of TALDO1 expression in 115 paraffin-embedded tumor samples from patients with UTUC using immunohistochemistry. Our results demonstrated that there was an association between high TALDO1 expression and advanced stage (P = 0.011), tumor size (P = 0.005), tumor location (P = 0.047), distant metastases (P = 0.023), local recurrence (P = 0.002), and cancer death (P = 0.003). Using univariate and multivariate analyses, we found that chemotherapy was an independent factor for bladder recurrence-free survival. Late stage (III/IV) and high TALDO1 expression were independent prognostic factors for progression-free and cancer-specific survival. In summary, increased TALDO1 expression in UTUC was significantly correlated with late stage, tumor size, tumor location, distant metastases, local recurrence, and cancer death. Therefore, high TALDO1 expression could be a predictor of poor survival in patients with UTUC. Further studies are necessary to investigate the role of TALDO1 in UTUC development.<br /> (© 2021 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd.)

Details

Language :
English
ISSN :
1440-1827
Volume :
71
Issue :
7
Database :
MEDLINE
Journal :
Pathology international
Publication Type :
Academic Journal
Accession number :
33848380
Full Text :
https://doi.org/10.1111/pin.13101