Over-expression of Wilm’s Tumor Gene 1 (WT1) in Iranian Patients with Acute Myeloblastic Leukemia

Authors

  • Abdolfattah Sarrafnejad Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  • Fazel Shokri Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran | Monoclonal Antibody Research Center, Avesina Research Institute, Tehran, Iran | National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran
  • Hodjatallah Rabbani Immune and Gene Therapy Lab, Cancer Center Karolinska, Karolinska Hospital, Stockholm, Sweden | Monoclonal Antibody Research Center, Avesina Research Institute, Tehran, Iran
  • Hossein Asgarian Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  • Jalal Khoshnoodi Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  • Mahdi Shabani Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  • Mahin Kordmahin Clinic of Hematology and Oncology, Vali-Asr Hospital, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Mahmood Jeddi Tehrani Immune and Gene Therapy Lab, Cancer Center Karolinska, Karolinska Hospital, Stockholm, Sweden | Monoclonal Antibody Research Center, Avesina Research Institute, Tehran, Iran
  • Parvaneh Vosoogh Clinic of Hematology, Ali-Asghar Hospital, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  • Ramazan Ali Sharifian Clinic of Hematology and Oncology, Vali-Asr Hospital, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Soheila Gharagozlou Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  • Tahereh Shahrestani Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
Abstract:

Background: The Wilm’s tumor gene 1 (WT1) encodes a zinc finger transcription factor that is inactivated in a subset of Wilm’s tumors. It plays a crucial role in growth, proliferation and development of some embryonic and adult organs. WT1 is expressed as a tumor associated antigen (TAA) in various types of solid and hematopoietic malignancies and can be employed as a useful marker for targeted immunotherapy and monitoring of minimal residual disease (MRD). Objective: To investigate the profile of WT1 gene expression in Iranian patients with acute myeloblastic leukemia. Methods: RT-PCR method was used to determine the WT1 gene expression in bone marrow (BM) and/or peripheral blood (PB) samples from 11 patients with AML and PB samples of 36 normal subjects. Isolated cells from all patients were immunophenotyped by flow cytometry. Results: The leukemic cells from 10 patients (91%) were found moderately or strongly positive for WT1 expression whereas only 3 out of 36 normal subjects expressed WT1 at very low levels. A highly significant correlation was observed for WT1 expression between paired BM and PB samples of the AML patients. Conclusion: Our results indicate that WT1 is expressed in the majority of Iranian AML patients and may be employed for screening and monitoring of minimal residual disease in these patients.

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Journal title

volume 2  issue 4

pages  182- 190

publication date 2005-12-01

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