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Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia

Inhibitor of beta-catenin and TCF (ICAT) is a key protein in the Wnt-β-catenin signaling pathway. However, its role in acute myeloid leukemia (AML) remains unknown. In this study, we evaluated its expression level as well as its prognostic value in AML patients. A total of 72 patients with AML and 3...

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Autores principales: Han, Hui, Zhu, Baofang, Xie, Jinye, Huang, Yunxiu, Geng, Yiyun, Chen, Kang, Wang, Weijia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387945/
https://www.ncbi.nlm.nih.gov/pubmed/35984200
http://dx.doi.org/10.1097/MD.0000000000030022
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author Han, Hui
Zhu, Baofang
Xie, Jinye
Huang, Yunxiu
Geng, Yiyun
Chen, Kang
Wang, Weijia
author_facet Han, Hui
Zhu, Baofang
Xie, Jinye
Huang, Yunxiu
Geng, Yiyun
Chen, Kang
Wang, Weijia
author_sort Han, Hui
collection PubMed
description Inhibitor of beta-catenin and TCF (ICAT) is a key protein in the Wnt-β-catenin signaling pathway. However, its role in acute myeloid leukemia (AML) remains unknown. In this study, we evaluated its expression level as well as its prognostic value in AML patients. A total of 72 patients with AML and 30 control subjects were enrolled in this study during the period of January 2017 and December 2019 at Zhongshan Hospital of SunYat-sen University. ICAT and β-catenin expression levels in peripheral blood were determined via enzyme-linked immunosorbent assays. ICAT levels in AML patients were significantly lower and β-catenin levels were higher than those of the control group. After the first course of standard chemotherapy, the concentration of ICAT in the partial remission group (93.79 ng/mL) was significantly higher than that in the initial diagnosis group (49.38 ng/mL) and the no response group (39.94 ng/mL). AML subtypes had lower ICAT expression levels than controls, and ICAT levels were significantly correlated with body mass index, bone marrow/peripheral blood blast cell proportions, and white blood cell and red blood cell counts at initial diagnosis. Furthermore, low ICAT expression was found to be associated with poor disease-free survival and overall survival in AML. ICAT is closely associated with AML progression and can be used as an indicator to monitor AML treatment efficacy.
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spelling pubmed-93879452022-08-23 Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia Han, Hui Zhu, Baofang Xie, Jinye Huang, Yunxiu Geng, Yiyun Chen, Kang Wang, Weijia Medicine (Baltimore) Research Article Inhibitor of beta-catenin and TCF (ICAT) is a key protein in the Wnt-β-catenin signaling pathway. However, its role in acute myeloid leukemia (AML) remains unknown. In this study, we evaluated its expression level as well as its prognostic value in AML patients. A total of 72 patients with AML and 30 control subjects were enrolled in this study during the period of January 2017 and December 2019 at Zhongshan Hospital of SunYat-sen University. ICAT and β-catenin expression levels in peripheral blood were determined via enzyme-linked immunosorbent assays. ICAT levels in AML patients were significantly lower and β-catenin levels were higher than those of the control group. After the first course of standard chemotherapy, the concentration of ICAT in the partial remission group (93.79 ng/mL) was significantly higher than that in the initial diagnosis group (49.38 ng/mL) and the no response group (39.94 ng/mL). AML subtypes had lower ICAT expression levels than controls, and ICAT levels were significantly correlated with body mass index, bone marrow/peripheral blood blast cell proportions, and white blood cell and red blood cell counts at initial diagnosis. Furthermore, low ICAT expression was found to be associated with poor disease-free survival and overall survival in AML. ICAT is closely associated with AML progression and can be used as an indicator to monitor AML treatment efficacy. Lippincott Williams & Wilkins 2022-08-19 /pmc/articles/PMC9387945/ /pubmed/35984200 http://dx.doi.org/10.1097/MD.0000000000030022 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Research Article
Han, Hui
Zhu, Baofang
Xie, Jinye
Huang, Yunxiu
Geng, Yiyun
Chen, Kang
Wang, Weijia
Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title_full Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title_fullStr Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title_full_unstemmed Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title_short Expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
title_sort expression level and prognostic potential of beta-catenin–interacting protein in acute myeloid leukemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387945/
https://www.ncbi.nlm.nih.gov/pubmed/35984200
http://dx.doi.org/10.1097/MD.0000000000030022
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