Title of article :
Evaluation of PPP2R5C gene expression in Iranian patients with B-Acute lymphoblastic leukemia and its association with clinical and laboratory findings
Author/Authors :
Rostami ، Esmaeil Department of Laboratory Sciences - Faculty of Paramedicine - Sabzevar University of Medical Sciences , Ayatollahi ، Hossein Department of Hematology and Blood Bank - Faculty of Medicine, Cancer Molecular Pathology Research Center - Mashhad University of Medical Sciences , Boustani ، Hassan Department of Hematology - School of Allied Medical Sciences - Iran University of Medical Sciences , Ghotaslou ، Abbas Department of Hematology - School of Allied Medical Sciences - Iran University of Medical Sciences , Sadeghian ، Mohammad Hadi Faculty of Medicine, Neonatal Research Center, Imam Reza Hospital - Mashhad University of Medical Sciences , Keramati ، Mohammad Reza Faculty of Medicine, Neonatal Research Center, Imam Reza Hospital - Mashhad University of Medical Sciences , Zeinali ، Elahe Department of laboratory sciences - Faculty of Paramedicine - Mashhad University of Medical Sciences , Rad ، Abolfazl Department of Biochemistry and Nutrition - Cellular and Molecular Research Center - Sabzevar University of Medical Sciences
Abstract :
Introduction: PPP2R5C is one of the regulatory B subunits of protein phosphatase 2A (PP2A), which is a tumor suppressor. PPP2R5C plays a critical role in cell proliferation, differentiation, and transformation. Considering these vital functions, we investigate the gene expression in Iranian patients with B-Acute Lymphoblastic Leukemia (B-ALL) and its association with clinical and laboratory finding. Materials and methods: In this case-control study, peripheral blood samples were collected from 60 B-ALL patients and 30 healthy controls. PPP2R5C expression levels were determined by Real-time PCR. After calculation of CT for target and control genes, we calculated ΔCT. Finally we compared the PPP2R5C expression levels in patients with control group. Results: Significantly higher expression of PPP2R5C was found in the B-ALL patients (2.15±2. 50) compared with control group. There was no correlation between PPP2R5C expression and clinical and laboratory findings and FAB (French-American-British) subtype of patients. Conclusion: we demonstrated PPP2R5C overexpression in B-ALL patients. Although there was no significant correlation between PPP2R5C expression, clinical and laboratory finding and also with FAB subtypes of patients.
Keywords :
B , Acute Lymphoblastic Leukemia , PPP2R5C , PP2A , Gene expression
Journal title :
Journal of Basic Research in Medical Sciences
Journal title :
Journal of Basic Research in Medical Sciences