Cargando…

Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report

BACKGROUND: In myelodysplastic syndrome (MDS), oxidative stress is closely related to iron overload and DNA damage. A recent study suggested the possibility that increased oxidative stress causes not only iron overload but also disease progression of MDS with DNA damage. We present a case of MDS wit...

Descripción completa

Detalles Bibliográficos
Autores principales: Hasunuma, Hidekazu, Shimizu, Naomi, Yokota, Hiromitsu, Tatsuno, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716315/
https://www.ncbi.nlm.nih.gov/pubmed/33344557
http://dx.doi.org/10.12998/wjcc.v8.i22.5657
_version_ 1783619133616685056
author Hasunuma, Hidekazu
Shimizu, Naomi
Yokota, Hiromitsu
Tatsuno, Ichiro
author_facet Hasunuma, Hidekazu
Shimizu, Naomi
Yokota, Hiromitsu
Tatsuno, Ichiro
author_sort Hasunuma, Hidekazu
collection PubMed
description BACKGROUND: In myelodysplastic syndrome (MDS), oxidative stress is closely related to iron overload and DNA damage. A recent study suggested the possibility that increased oxidative stress causes not only iron overload but also disease progression of MDS with DNA damage. We present a case of MDS with decreased reactive oxygen species (ROS) production in peripheral white blood cells (WBCs) and decreased diacron-reactive oxygen metabolites (d-ROMs) in serum after azacitidine therapy. CASE SUMMARY: A 74-year-old man presented to the hematological department with the chief complaint of anemia. His vital signs were within normal limits at admission with a heart rate of 80 bpm and blood pressure of 135/60 mmHg. Laboratory tests indicated pancytopenia, a WBC count of 2190 cells/µL, a hemoglobin level of 6.2 g/dL and a platelet count of 7.4 × 10(4)/µL. The patient was diagnosed with MDS with fibrosis after a bone marrow examination. This case showed decreased ROS production in WBCs, d-ROMs in serum and Wilms’ tumor 1 after azacitidine therapy, after which his hematopoiesis recovered. CONCLUSION: Azacitidine therapy can improve hematopoiesis and decrease ROS and d-ROM production.
format Online
Article
Text
id pubmed-7716315
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Baishideng Publishing Group Inc
record_format MEDLINE/PubMed
spelling pubmed-77163152020-12-18 Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report Hasunuma, Hidekazu Shimizu, Naomi Yokota, Hiromitsu Tatsuno, Ichiro World J Clin Cases Case Report BACKGROUND: In myelodysplastic syndrome (MDS), oxidative stress is closely related to iron overload and DNA damage. A recent study suggested the possibility that increased oxidative stress causes not only iron overload but also disease progression of MDS with DNA damage. We present a case of MDS with decreased reactive oxygen species (ROS) production in peripheral white blood cells (WBCs) and decreased diacron-reactive oxygen metabolites (d-ROMs) in serum after azacitidine therapy. CASE SUMMARY: A 74-year-old man presented to the hematological department with the chief complaint of anemia. His vital signs were within normal limits at admission with a heart rate of 80 bpm and blood pressure of 135/60 mmHg. Laboratory tests indicated pancytopenia, a WBC count of 2190 cells/µL, a hemoglobin level of 6.2 g/dL and a platelet count of 7.4 × 10(4)/µL. The patient was diagnosed with MDS with fibrosis after a bone marrow examination. This case showed decreased ROS production in WBCs, d-ROMs in serum and Wilms’ tumor 1 after azacitidine therapy, after which his hematopoiesis recovered. CONCLUSION: Azacitidine therapy can improve hematopoiesis and decrease ROS and d-ROM production. Baishideng Publishing Group Inc 2020-11-26 2020-11-26 /pmc/articles/PMC7716315/ /pubmed/33344557 http://dx.doi.org/10.12998/wjcc.v8.i22.5657 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Hasunuma, Hidekazu
Shimizu, Naomi
Yokota, Hiromitsu
Tatsuno, Ichiro
Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title_full Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title_fullStr Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title_full_unstemmed Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title_short Azacitidine decreases reactive oxygen species production in peripheral white blood cells: A case report
title_sort azacitidine decreases reactive oxygen species production in peripheral white blood cells: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716315/
https://www.ncbi.nlm.nih.gov/pubmed/33344557
http://dx.doi.org/10.12998/wjcc.v8.i22.5657
work_keys_str_mv AT hasunumahidekazu azacitidinedecreasesreactiveoxygenspeciesproductioninperipheralwhitebloodcellsacasereport
AT shimizunaomi azacitidinedecreasesreactiveoxygenspeciesproductioninperipheralwhitebloodcellsacasereport
AT yokotahiromitsu azacitidinedecreasesreactiveoxygenspeciesproductioninperipheralwhitebloodcellsacasereport
AT tatsunoichiro azacitidinedecreasesreactiveoxygenspeciesproductioninperipheralwhitebloodcellsacasereport