Searchfield, Lydia ![]() ![]() |
Abstract
Aims: Renal cell carcinoma (RCC) often recurs as distant metastasis; there is thus a need for new indicators to identify high-risk patients. Glutathione S-transferases (GST)- and -π are involved in the renal bioactivation of toxic metabolites. The aim was to investigate whether their expression is of diagnostic and prognostic value. Methods and results: Western blotting of microdissected normal kidney and immunostaining of histological RCC microarrays shows expression of GST- in proximal tubular cells, while GST-π was found in the distal nephron. Of the primary 174 RCC cases examined, GST- immunoreactivity was restricted to conventional RCC (n = 76, 68% positive) and was not seen in any other RCC subtypes. The cross-tabulation of the GST- scores with other prognostic indices demonstrated that GST- immunostaining was significantly more frequent in low-grade tumours (χ2: P < 0.004), and that conventional GST--positive RCC patients had a mean disease-free survival of 6.0 years (95% confidence interval 5.33–6.63), compared with 4.7 years (3.54–5.90) in GST--negative tumours (Kaplan–Meier survival analysis, P = 0.011, log-rank test). Conclusions: GST- is a highly specific diagnostic marker for primary conventional RCC, where it is a prognostic marker if grade is omitted from the multivariate analysis.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Biosciences Medicine |
Subjects: | Q Science > Q Science (General) R Medicine > R Medicine (General) |
Uncontrolled Keywords: | 3,3′-diaminobenzidine; glutathione S-transferases; horseradish peroxidase; immunohistochemistry; prognostic indicators; renal cell carcinoma; tissue microarray; Western blotting |
Publisher: | Wiley |
ISSN: | 0309-0167 |
Last Modified: | 29 Aug 2024 01:08 |
URI: | https://orca.cardiff.ac.uk/id/eprint/23049 |
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