Author/Authors :
Zahedi Avval Farnaz نويسنده Department of Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, IR Iran , Lorestani Shima نويسنده Department of Clinical Biochemistry, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran , Hashemy Seyyed Isaac نويسنده Department of Clinical Biochemistry, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran , Mojarad Majid نويسنده Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran , Keyvanloo Shahrestanaki Mohammad نويسنده Department of Clinical Biochemistry, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran , Bahari Ali نويسنده Endoscopic and Minimally Invasive Surgery Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran , Asadi Mahdi نويسنده Surgical Oncology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Background: Glutathione reductase is an important enzyme in oxidative metabolism
that provides reduced glutathione from its oxidized form in the cells. The role of
oxidative stress in tumor tissues has led us to investigate the gene expression and activity
of this enzyme in tumor and adjacent resected margins of colorectal cancer tissues,
one of the most common malignancies in humans.
Methods: We conducted this study on 15 Iranian colorectal cancer patients. RNA
was extracted from fresh colon tissues that included tumor and anatomically normal
margin tissue. Expression of the glutathione reductase gene was determined using realtime
PCR by the ??Ct relative quantification method. The gene expression results were
standardized with glyceraldehyde 3-phosphate dehydrogenase as the endogenous
reference gene. In addition, we measured enzyme activity of glutathione reductase with
a commercial kit based on a colorimetric assay.
Results: The tumor tissue had higher expression of glutathione reductase compared
to the margin tissue (P=0.005). There was significantly greater glutathione reductase
enzyme activity in the tumor tissue (116.9±34.31 nmol/min/ml) compared to the noncancerous
adjacent tissues (76.7±36.85 nmol/min/ml; P=0.003).
Conclusion: These data showed increased glutathione reductase expression and
enzyme activity in colorectal tumor tissue. Given the key role of glutathione in
synthesis of dNTPs for DNA repair with the glutaredoxin system, the increased
glutathione reductase expression and activity might be a reflection of hyperactivity of
this enzyme in DNA synthesis and the repair process in colorectal cancer cells.