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...

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Published in:Medicine (Baltimore) Vol. 101; no. 33; p. e30022
Main Authors: Han, Hui, Zhu, Baofang, Xie, Jinye, Huang, Yunxiu, Geng, Yiyun, Chen, Kang, Wang, Weijia
Format: Journal Article
Language:English
Published: United States Lippincott Williams & Wilkins 19-08-2022
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Summary: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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ISSN:1536-5964
0025-7974
1536-5964
DOI:10.1097/MD.0000000000030022