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Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias

It has recently been shown that ROR1, a member of the receptor tyrosine kinase family, is overexpressed in leukemic B cells of Chronic Lymphocytic Leukemia (CLL) and a subset of Acute Lymphoblastic Leukemia (ALL). In this comparative study the expression profile of ROR1 mRNA was investigated in Iran...

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Autores principales: Shabani, Mahdi, Omran, Hossein Asgarian, Farsangi, Mohammad Hojjat, Vossough, Parvaneh, Sharifian, Ramazan A., Toughe, Gholam R., Razavi, Seyed Mohsen, Khoshnoodi, Jalal, Jeddi-Tehrani, Mahmood, Rabbani, Hodjatallah, Shokri, Fazel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558186/
https://www.ncbi.nlm.nih.gov/pubmed/23408747
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author Shabani, Mahdi
Omran, Hossein Asgarian
Farsangi, Mohammad Hojjat
Vossough, Parvaneh
Sharifian, Ramazan A.
Toughe, Gholam R.
Razavi, Seyed Mohsen
Khoshnoodi, Jalal
Jeddi-Tehrani, Mahmood
Rabbani, Hodjatallah
Shokri, Fazel
author_facet Shabani, Mahdi
Omran, Hossein Asgarian
Farsangi, Mohammad Hojjat
Vossough, Parvaneh
Sharifian, Ramazan A.
Toughe, Gholam R.
Razavi, Seyed Mohsen
Khoshnoodi, Jalal
Jeddi-Tehrani, Mahmood
Rabbani, Hodjatallah
Shokri, Fazel
author_sort Shabani, Mahdi
collection PubMed
description It has recently been shown that ROR1, a member of the receptor tyrosine kinase family, is overexpressed in leukemic B cells of Chronic Lymphocytic Leukemia (CLL) and a subset of Acute Lymphoblastic Leukemia (ALL). In this comparative study the expression profile of ROR1 mRNA was investigated in Iranian patients with CLL and Acute Myelogenous Leukemia (AML) and the results were compared with those previously reported in our Iranian ALL patients. RT-PCR was performed on bone marrow and/or peripheral blood samples of 84 CLL and 12 AML patients. CLL samples were classified into immunoglobulin heavy chain variable region (IGHV) gene mutated (n = 55) and unmutated (n = 29) and also indolent (n = 42) and progressive (n = 39) subtypes. ROR1 expression was identified in 94% of our CLL patients, but none of the AML patients expressed ROR1. No significant differences were observed between different CLL subtypes for ROR1 expression. Taken together the present data and our previous results on ROR1 expression in ALL, our findings propose ROR1 as a tumor-associated antigen overexpressed in a large proportion of lymphoid (CLL and ALL), but not myeloid (AML) leukemias. Expression of ROR1 seems to be associated to lineage and differentiation stages of leukemic cells with a potential implication for immunotherapy.
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spelling pubmed-35581862013-02-13 Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias Shabani, Mahdi Omran, Hossein Asgarian Farsangi, Mohammad Hojjat Vossough, Parvaneh Sharifian, Ramazan A. Toughe, Gholam R. Razavi, Seyed Mohsen Khoshnoodi, Jalal Jeddi-Tehrani, Mahmood Rabbani, Hodjatallah Shokri, Fazel Avicenna J Med Biotechnol Original Article It has recently been shown that ROR1, a member of the receptor tyrosine kinase family, is overexpressed in leukemic B cells of Chronic Lymphocytic Leukemia (CLL) and a subset of Acute Lymphoblastic Leukemia (ALL). In this comparative study the expression profile of ROR1 mRNA was investigated in Iranian patients with CLL and Acute Myelogenous Leukemia (AML) and the results were compared with those previously reported in our Iranian ALL patients. RT-PCR was performed on bone marrow and/or peripheral blood samples of 84 CLL and 12 AML patients. CLL samples were classified into immunoglobulin heavy chain variable region (IGHV) gene mutated (n = 55) and unmutated (n = 29) and also indolent (n = 42) and progressive (n = 39) subtypes. ROR1 expression was identified in 94% of our CLL patients, but none of the AML patients expressed ROR1. No significant differences were observed between different CLL subtypes for ROR1 expression. Taken together the present data and our previous results on ROR1 expression in ALL, our findings propose ROR1 as a tumor-associated antigen overexpressed in a large proportion of lymphoid (CLL and ALL), but not myeloid (AML) leukemias. Expression of ROR1 seems to be associated to lineage and differentiation stages of leukemic cells with a potential implication for immunotherapy. Avicenna Research Institute 2011 /pmc/articles/PMC3558186/ /pubmed/23408747 Text en Copyright © 2011 Avicenna Research Institute http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Shabani, Mahdi
Omran, Hossein Asgarian
Farsangi, Mohammad Hojjat
Vossough, Parvaneh
Sharifian, Ramazan A.
Toughe, Gholam R.
Razavi, Seyed Mohsen
Khoshnoodi, Jalal
Jeddi-Tehrani, Mahmood
Rabbani, Hodjatallah
Shokri, Fazel
Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title_full Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title_fullStr Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title_full_unstemmed Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title_short Comparative Expression Profile of Orphan Receptor Tyrosine Kinase ROR1 in Iranian Patients with Lymphoid and Myeloid Leukemias
title_sort comparative expression profile of orphan receptor tyrosine kinase ror1 in iranian patients with lymphoid and myeloid leukemias
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558186/
https://www.ncbi.nlm.nih.gov/pubmed/23408747
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