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 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Lippincott Williams & Wilkins
19-08-2022
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Subjects: | |
Online Access: | Get full text |
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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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1536-5964 0025-7974 1536-5964 |
DOI: | 10.1097/MD.0000000000030022 |