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FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients

Background: FAT atypical cadherin 1 (FAT1) is a member of the cadherin superfamily whose loss or gain is associated with the initiation and/or progression of different cancers. FAT1 overexpression has been reported in hematological malignancies. This research intended to investigate FAT1 gene expres...

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Autores principales: Ostadali Dehagi, Mohammadreza, Rostami, Shahrbano, Shamshiri, Ahmadreza, Safari, Fatemeh, Haji Hosseini, Reza, Thorne, Rick F, Ghavamzadeh, Ardeshir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452949/
https://www.ncbi.nlm.nih.gov/pubmed/37637767
http://dx.doi.org/10.18502/ijhoscr.v17i2.12644
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author Ostadali Dehagi, Mohammadreza
Rostami, Shahrbano
Shamshiri, Ahmadreza
Safari, Fatemeh
Haji Hosseini, Reza
Thorne, Rick F
Ghavamzadeh, Ardeshir
author_facet Ostadali Dehagi, Mohammadreza
Rostami, Shahrbano
Shamshiri, Ahmadreza
Safari, Fatemeh
Haji Hosseini, Reza
Thorne, Rick F
Ghavamzadeh, Ardeshir
author_sort Ostadali Dehagi, Mohammadreza
collection PubMed
description Background: FAT atypical cadherin 1 (FAT1) is a member of the cadherin superfamily whose loss or gain is associated with the initiation and/or progression of different cancers. FAT1 overexpression has been reported in hematological malignancies. This research intended to investigate FAT1 gene expression in adult Iranian acute leukemia patients, compared to normal mobilized peripheral blood CD34+ cells. Materials and Methods: The peripheral blast (peripheral blood mononuclear cells) cells of 22 acute myeloid leukemia (AML), 14 acute lymphoid leukemia (ALL) patients, and mobilized peripheral blood CD34+ cells of 12 healthy volunteer stem cell donors were collected. Then, quantitative real-time polymerase chain reaction (qPCR) was used to compare FAT1 gene expression. Results: Overall, there were no significant differences in FAT1 expression between AML and ALL patients (p>0.2). Nonetheless, the mean expression level of FAT1 was significantly higher in leukemic patients (AML and ALL) than in normal CD34+ cells (p=0.029). Additionally, the FAT1 expression levels were significantly higher in both CD34+ and CD34- leukemic patients than in normal CD34+ cells (p=0.028). Conclusion: No significant differences were found between FAT1 expression in CD34+ and CD34- leukemic samples (p> 0.3). Thus, higher FAT1 expression was evident in ALL and AML leukemia cells but this appeared unrelated to CD34 expression. This suggests in a proportion of adult acute leukemia, FAT1 expression may prove to be a suitable target for therapeutic strategies.
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spelling pubmed-104529492023-08-26 FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients Ostadali Dehagi, Mohammadreza Rostami, Shahrbano Shamshiri, Ahmadreza Safari, Fatemeh Haji Hosseini, Reza Thorne, Rick F Ghavamzadeh, Ardeshir Int J Hematol Oncol Stem Cell Res Original Article Background: FAT atypical cadherin 1 (FAT1) is a member of the cadherin superfamily whose loss or gain is associated with the initiation and/or progression of different cancers. FAT1 overexpression has been reported in hematological malignancies. This research intended to investigate FAT1 gene expression in adult Iranian acute leukemia patients, compared to normal mobilized peripheral blood CD34+ cells. Materials and Methods: The peripheral blast (peripheral blood mononuclear cells) cells of 22 acute myeloid leukemia (AML), 14 acute lymphoid leukemia (ALL) patients, and mobilized peripheral blood CD34+ cells of 12 healthy volunteer stem cell donors were collected. Then, quantitative real-time polymerase chain reaction (qPCR) was used to compare FAT1 gene expression. Results: Overall, there were no significant differences in FAT1 expression between AML and ALL patients (p>0.2). Nonetheless, the mean expression level of FAT1 was significantly higher in leukemic patients (AML and ALL) than in normal CD34+ cells (p=0.029). Additionally, the FAT1 expression levels were significantly higher in both CD34+ and CD34- leukemic patients than in normal CD34+ cells (p=0.028). Conclusion: No significant differences were found between FAT1 expression in CD34+ and CD34- leukemic samples (p> 0.3). Thus, higher FAT1 expression was evident in ALL and AML leukemia cells but this appeared unrelated to CD34 expression. This suggests in a proportion of adult acute leukemia, FAT1 expression may prove to be a suitable target for therapeutic strategies. Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2023-04-01 /pmc/articles/PMC10452949/ /pubmed/37637767 http://dx.doi.org/10.18502/ijhoscr.v17i2.12644 Text en Copyright © 2023 Tehran University of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Ostadali Dehagi, Mohammadreza
Rostami, Shahrbano
Shamshiri, Ahmadreza
Safari, Fatemeh
Haji Hosseini, Reza
Thorne, Rick F
Ghavamzadeh, Ardeshir
FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title_full FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title_fullStr FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title_full_unstemmed FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title_short FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients
title_sort fat1 gene expression in iranian acute lymphoid and myeloid leukemia patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452949/
https://www.ncbi.nlm.nih.gov/pubmed/37637767
http://dx.doi.org/10.18502/ijhoscr.v17i2.12644
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