Translational Research
Volume 155, Issue 5 , Pages 256-262, May 2010

Isoenzyme profile of glutathione transferases in transitional cell carcinoma of upper urinary tract

  • Marija Matic

      Affiliations

    • Institute of Medical and Clinical Biochemistry, University of Belgrade, Belgrade, Serbia
  • ,
  • Tatjana Simic

      Affiliations

    • Institute of Medical and Clinical Biochemistry, University of Belgrade, Belgrade, Serbia
  • ,
  • Dejan Dragicevic

      Affiliations

    • Institute of Urology and Nephrology Faculty of Medicine, University of Belgrade, Belgrade, Serbia
  • ,
  • Jasmina Mimic-Oka

      Affiliations

    • Institute of Medical and Clinical Biochemistry, University of Belgrade, Belgrade, Serbia
  • ,
  • Marija Pljesa-Ercegovac

      Affiliations

    • Institute of Medical and Clinical Biochemistry, University of Belgrade, Belgrade, Serbia
  • ,
  • Ana Savic-Radojevic

      Affiliations

    • Institute of Medical and Clinical Biochemistry, University of Belgrade, Belgrade, Serbia
    • Corresponding Author InformationReprint requests: Ana Savic-Radojevic, MD, PhD, Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, Pasterova 2, 11000 Belgrade, Serbia

Received 21 August 2009; received in revised form 16 October 2009; accepted 16 November 2009. published online 18 December 2009.

Upregulated glutathione S-transferase P1 (GSTP1) plays an important role in the resistance to apoptosis in transitional cell carcinoma (TCC) of the urinary bladder (UB) and represents a potential target for chemotherapeutic agents. Our aim was to perform a systematic investigation of a glutathione S-transferase (GST) isoenzyme profile (GSTM, GSTP1, and GSTT1) in the upper urinary tract (UUT) TCC and compare it with the GST isoenzyme pattern of the UB TCC and normal urothelium. We examined GST activity spectrophotometrically by using substrates for the overall GST activity, GSTP1, and GSTT1 in the cytosolic fraction. GSTP1 and GSTM expression was analyzed by Western blotting. The results obtained have shown that the overall GST activity was significantly higher in UUT TCC in comparison with urothelium (P<0.001), which gradually increases with tumor grade (P<0.05). The mean GSTP1 and GSTT1 activities in UUT TCC were 2- and 3.6-fold higher, respectively, than in the normal urothelium (P<0.001), and these values did not differ significantly from activities found in the UB TCC. GSTM was expressed in 42% of the UUT TCC and 50% of the UB TCC specimens. The level of GSTM expression was slightly increased in the UUT TCC specimens in comparison with normal urothelium (P>0.05). We conclude that 3 major cytosolic GST classes, GSTM, GSTP1, and GSTT1, are expressed in the UUT TCC. The isoenzyme profile of GST in the UUT TCC is similar to that observed in the UB TCC; it shows essentially the same alteration of the GST phenotype in the course of cancerization. The association of GSTT1 and GSTP1 upregulation with the malignant phenotype of the UUT TCC might result in resistances to both chemotherapy and apoptosis.

Abbreviations: BEN, Balkan endemic nephropathy, CDNB, 1-chloro-2,4-dinitrobenzene, EPNP, 1,2-epoxy-3-(p-nitrophenoxy)propane, GSH, glutathione, GST, glutathione S-transferase, GSTM, GST Mu, GSTP, GST Pi, GSTT, GST Theta, JNK, c-Jun NH2-terminal kinase, TCC, transitional cell carcinoma, UB, urinary bladder, UUT, upper urinary tract, VP, 4-vinyl-pyridine

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 Supported by Grant 145009DJ from the Serbian Ministry of Science.

PII: S1931-5244(09)00341-7

doi:10.1016/j.trsl.2009.11.001

Translational Research
Volume 155, Issue 5 , Pages 256-262, May 2010