Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)

Background and Aim: Chronic myelogenous leukemia is characterized by Philadelphia (Ph) chromosome, the presence of BCR-ABL fusion gene and constitutive activation of the ABL1 tyrosine kinase. Despite an excellent result of target therapy by imatinib, some patients develop resistance to imatinib. In...

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Main Authors: Mahdihe Ghasemi, Fatemeh Nadali, Seyed Naser Ostad, Farhad Zaker, Shahrbanoo Rostamy, Hossein Dargahi
Format: Article
Language:fas
Published: Tehran University of Medical Sciences 2012-12-01
Series:پیاورد سلامت
Subjects:
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/22749.pdf&manuscript_id=22749
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spelling doaj-5a31ca40aa49431caf8dd9a188bae4ad2021-10-02T01:19:41ZfasTehran University of Medical Sciencesپیاورد سلامت1735-81322008-26652012-12-0164282292Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)Mahdihe GhasemiFatemeh NadaliSeyed Naser OstadFarhad ZakerShahrbanoo RostamyHossein DargahiBackground and Aim: Chronic myelogenous leukemia is characterized by Philadelphia (Ph) chromosome, the presence of BCR-ABL fusion gene and constitutive activation of the ABL1 tyrosine kinase. Despite an excellent result of target therapy by imatinib, some patients develop resistance to imatinib. In this study Efficacy of HESA-A on proliferation and apoptosis of K562 cell line was assessed. Materials and Methods: In this study doubling time of K562 cell line was calculated. The cells were affected by various concentrations of HESA-A(1,2,4 and 8 mg/ml respectively). Cytotoxicity and IC50 dose of HESA-A were detected by MTT and trypan blue exclusion assay. Apoptosis was assessed by flowcytometry after 48 h cell treatment in the presence of IC50 dose. Results: Doubling time of K562 cells was 24 hours. HESA-A reduced the number of viable K562 cells in a concentration dependent manner.IC50 dose was 3.5 mg/ml. In flowcytometry analysis of apoptosis, 19.22% of the treated cells were located in the position of the necrotic cells. Conclusion: The results of MTT and trypan blue exclusion assay suggest that HESA-A inhibits the growth of k562 cells in a concentration dependent manner and induces necrosis in K562 cells.http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/22749.pdf&manuscript_id=22749Chronic Myelogenous LeukemiaHESA-ACytotoxicityApoptosis
collection DOAJ
language fas
format Article
sources DOAJ
author Mahdihe Ghasemi
Fatemeh Nadali
Seyed Naser Ostad
Farhad Zaker
Shahrbanoo Rostamy
Hossein Dargahi
spellingShingle Mahdihe Ghasemi
Fatemeh Nadali
Seyed Naser Ostad
Farhad Zaker
Shahrbanoo Rostamy
Hossein Dargahi
Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
پیاورد سلامت
Chronic Myelogenous Leukemia
HESA-A
Cytotoxicity
Apoptosis
author_facet Mahdihe Ghasemi
Fatemeh Nadali
Seyed Naser Ostad
Farhad Zaker
Shahrbanoo Rostamy
Hossein Dargahi
author_sort Mahdihe Ghasemi
title Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
title_short Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
title_full Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
title_fullStr Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
title_full_unstemmed Assesment Of The Efficacy Of HESA-A On The Proliferation And Apoptosis Of Chronic Myelogenous Leukemia Cell Line(K562)
title_sort assesment of the efficacy of hesa-a on the proliferation and apoptosis of chronic myelogenous leukemia cell line(k562)
publisher Tehran University of Medical Sciences
series پیاورد سلامت
issn 1735-8132
2008-2665
publishDate 2012-12-01
description Background and Aim: Chronic myelogenous leukemia is characterized by Philadelphia (Ph) chromosome, the presence of BCR-ABL fusion gene and constitutive activation of the ABL1 tyrosine kinase. Despite an excellent result of target therapy by imatinib, some patients develop resistance to imatinib. In this study Efficacy of HESA-A on proliferation and apoptosis of K562 cell line was assessed. Materials and Methods: In this study doubling time of K562 cell line was calculated. The cells were affected by various concentrations of HESA-A(1,2,4 and 8 mg/ml respectively). Cytotoxicity and IC50 dose of HESA-A were detected by MTT and trypan blue exclusion assay. Apoptosis was assessed by flowcytometry after 48 h cell treatment in the presence of IC50 dose. Results: Doubling time of K562 cells was 24 hours. HESA-A reduced the number of viable K562 cells in a concentration dependent manner.IC50 dose was 3.5 mg/ml. In flowcytometry analysis of apoptosis, 19.22% of the treated cells were located in the position of the necrotic cells. Conclusion: The results of MTT and trypan blue exclusion assay suggest that HESA-A inhibits the growth of k562 cells in a concentration dependent manner and induces necrosis in K562 cells.
topic Chronic Myelogenous Leukemia
HESA-A
Cytotoxicity
Apoptosis
url http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/22749.pdf&manuscript_id=22749
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