In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients

Objective. Some, but not all, β-thalassemia/hemoglobin E (β-thal/HbE) patients respond to hydroxyurea treatment. It would be helpful if patient responses to hydroxyurea could be screened in vitro to identify responders and nonresponders before beginning in vivo treatment. Materials and Methods. Thir...

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Main Authors: Yuwadee Watanapokasin, Suporn Chuncharunee, Duangmanee Sanmund, Wantana Kongnium, Pranee Winichagoon, Griffin P. Rodgers, Suthat Fucharoen
Other Authors: Srinakharinwirot University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/16270
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spelling th-mahidol.162702018-06-21T15:20:32Z In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients Yuwadee Watanapokasin Suporn Chuncharunee Duangmanee Sanmund Wantana Kongnium Pranee Winichagoon Griffin P. Rodgers Suthat Fucharoen Srinakharinwirot University Mahidol University The Institute of Science and Technology for Research and Development, Mahidol University National Institute of Diabetes and Digestive and Kidney Diseases Biochemistry, Genetics and Molecular Biology Medicine Objective. Some, but not all, β-thalassemia/hemoglobin E (β-thal/HbE) patients respond to hydroxyurea treatment. It would be helpful if patient responses to hydroxyurea could be screened in vitro to identify responders and nonresponders before beginning in vivo treatment. Materials and Methods. Thirteen β-Thal/HbE patients were treated with hydroxyurea orally for 2 years at a starting dose of 5 mg/kg/day for 5 days/week with escalation to a maximum of 10 mg/kg/day. For comparison, erythroid cells obtained from peripheral blood of the same patients 1 year after they had stopped hydroxyurea treatment were treated with hydroxyurea in vitro. The γ-globin mRNA was measured by real-time reverse-transcription polymerase chain reaction, fetal hemoglobin (HbF) by high-performance liquid chromatography,Gγ- andAγ-globin chains by Triton X-100 acid urea polyacrylamide gel electrophoresis. Results. Treatment of cells in primary culture with 30 μM hydroxyurea for 96 hours significantly increased the fractional HbF content in β-Thal/HbE patients. TheGγ:Aγ-globin mRNA was induced 0.30- to 8-fold in vitro and 0.30- to 6-fold in vivo (r2= 0.51, p = 0.16 by paired t-test); the fractional HbF content was induced 0.50- to 19-fold in vitro and 0.30- to 12-fold in vivo (r2= 0.61, p = 0.20) and theGγ:Aγ-globin chain ratio was increased 0.80- to 1.40-fold in vitro and 1- to 1.20-fold in vivo (r2= 0.62, p = 0.13). Conclusion. The correlation of in vivo and in vitro results of HbF synthesis and globin mRNA suggest that in vitro testing may predict the in vivo response. © 2005 International Society for Experimental Hematology. Published by Elsevier Inc. 2018-06-21T08:07:35Z 2018-06-21T08:07:35Z 2005-12-01 Article Experimental Hematology. Vol.33, No.12 (2005), 1486-1492 10.1016/j.exphem.2005.09.006 0301472X 2-s2.0-28844471024 https://repository.li.mahidol.ac.th/handle/123456789/16270 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=28844471024&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Yuwadee Watanapokasin
Suporn Chuncharunee
Duangmanee Sanmund
Wantana Kongnium
Pranee Winichagoon
Griffin P. Rodgers
Suthat Fucharoen
In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
description Objective. Some, but not all, β-thalassemia/hemoglobin E (β-thal/HbE) patients respond to hydroxyurea treatment. It would be helpful if patient responses to hydroxyurea could be screened in vitro to identify responders and nonresponders before beginning in vivo treatment. Materials and Methods. Thirteen β-Thal/HbE patients were treated with hydroxyurea orally for 2 years at a starting dose of 5 mg/kg/day for 5 days/week with escalation to a maximum of 10 mg/kg/day. For comparison, erythroid cells obtained from peripheral blood of the same patients 1 year after they had stopped hydroxyurea treatment were treated with hydroxyurea in vitro. The γ-globin mRNA was measured by real-time reverse-transcription polymerase chain reaction, fetal hemoglobin (HbF) by high-performance liquid chromatography,Gγ- andAγ-globin chains by Triton X-100 acid urea polyacrylamide gel electrophoresis. Results. Treatment of cells in primary culture with 30 μM hydroxyurea for 96 hours significantly increased the fractional HbF content in β-Thal/HbE patients. TheGγ:Aγ-globin mRNA was induced 0.30- to 8-fold in vitro and 0.30- to 6-fold in vivo (r2= 0.51, p = 0.16 by paired t-test); the fractional HbF content was induced 0.50- to 19-fold in vitro and 0.30- to 12-fold in vivo (r2= 0.61, p = 0.20) and theGγ:Aγ-globin chain ratio was increased 0.80- to 1.40-fold in vitro and 1- to 1.20-fold in vivo (r2= 0.62, p = 0.13). Conclusion. The correlation of in vivo and in vitro results of HbF synthesis and globin mRNA suggest that in vitro testing may predict the in vivo response. © 2005 International Society for Experimental Hematology. Published by Elsevier Inc.
author2 Srinakharinwirot University
author_facet Srinakharinwirot University
Yuwadee Watanapokasin
Suporn Chuncharunee
Duangmanee Sanmund
Wantana Kongnium
Pranee Winichagoon
Griffin P. Rodgers
Suthat Fucharoen
format Article
author Yuwadee Watanapokasin
Suporn Chuncharunee
Duangmanee Sanmund
Wantana Kongnium
Pranee Winichagoon
Griffin P. Rodgers
Suthat Fucharoen
author_sort Yuwadee Watanapokasin
title In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
title_short In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
title_full In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
title_fullStr In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
title_full_unstemmed In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin E patients
title_sort in vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in β-thalassemia/hemoglobin e patients
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/16270
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