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Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer
Ezrin and adherens junction-associated protein 1 (AJAP1) are structural proteins which are involved in numerous human malignancies. However, little is known about the relationship between them in breast cancer. This study was set out to investigate the relationship between them and to further explor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931223/ https://www.ncbi.nlm.nih.gov/pubmed/35311087 http://dx.doi.org/10.3389/fonc.2022.831507 |
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author | Xu, Cong Wang, Feng Hao, Li Liu, Jing Shan, Benjie Lv, Shuhua Han, Xinghua Pan, Yueyin Niu, Yun |
author_facet | Xu, Cong Wang, Feng Hao, Li Liu, Jing Shan, Benjie Lv, Shuhua Han, Xinghua Pan, Yueyin Niu, Yun |
author_sort | Xu, Cong |
collection | PubMed |
description | Ezrin and adherens junction-associated protein 1 (AJAP1) are structural proteins which are involved in numerous human malignancies. However, little is known about the relationship between them in breast cancer. This study was set out to investigate the relationship between them and to further explore the mechanism of AJAP1-mediating cytoskeleton in breast cancer progression. Ezrin and AJAP1 expressions were detected in 377 samples of breast cancer by immunohistochemistry, and different expression patterns between AJAP1 and Ezrin with clinicopathological parameters were analyzed. Besides, univariate and multivariate Cox models were used to evaluate their prognostic potential. Enzyme-linked immunosorbent assay, Western blot, qRT-PCR, and phalloidin staining of F-actin were used to explore the relationship and the mechanism between AJAP1 and Ezrin in cytoskeleton arrangement. 377 cases of breast cancer results showed that AJAP1 expression was negatively related with histological grade and lymph node involvement and could be an independent prognosis marker of breast cancer. AJAP1 expression tended to be higher in the Ezrin-negative expression case. Patients with AJAP1(negative) and Ezrin(positive) expression had a worse prognosis (p < 0.0001) and shorter DFS (p = 0.015). More importantly, AJAP1 depletion increased the cell ability of F-actin formation through promoting Ezrin expression. AJAP1 depletion might mediate breast cancer malignancy potential through promoting Ezrin expression and cytoskeleton formation. |
format | Online Article Text |
id | pubmed-8931223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89312232022-03-19 Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer Xu, Cong Wang, Feng Hao, Li Liu, Jing Shan, Benjie Lv, Shuhua Han, Xinghua Pan, Yueyin Niu, Yun Front Oncol Oncology Ezrin and adherens junction-associated protein 1 (AJAP1) are structural proteins which are involved in numerous human malignancies. However, little is known about the relationship between them in breast cancer. This study was set out to investigate the relationship between them and to further explore the mechanism of AJAP1-mediating cytoskeleton in breast cancer progression. Ezrin and AJAP1 expressions were detected in 377 samples of breast cancer by immunohistochemistry, and different expression patterns between AJAP1 and Ezrin with clinicopathological parameters were analyzed. Besides, univariate and multivariate Cox models were used to evaluate their prognostic potential. Enzyme-linked immunosorbent assay, Western blot, qRT-PCR, and phalloidin staining of F-actin were used to explore the relationship and the mechanism between AJAP1 and Ezrin in cytoskeleton arrangement. 377 cases of breast cancer results showed that AJAP1 expression was negatively related with histological grade and lymph node involvement and could be an independent prognosis marker of breast cancer. AJAP1 expression tended to be higher in the Ezrin-negative expression case. Patients with AJAP1(negative) and Ezrin(positive) expression had a worse prognosis (p < 0.0001) and shorter DFS (p = 0.015). More importantly, AJAP1 depletion increased the cell ability of F-actin formation through promoting Ezrin expression. AJAP1 depletion might mediate breast cancer malignancy potential through promoting Ezrin expression and cytoskeleton formation. Frontiers Media S.A. 2022-03-04 /pmc/articles/PMC8931223/ /pubmed/35311087 http://dx.doi.org/10.3389/fonc.2022.831507 Text en Copyright © 2022 Xu, Wang, Hao, Liu, Shan, Lv, Han, Pan and Niu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Xu, Cong Wang, Feng Hao, Li Liu, Jing Shan, Benjie Lv, Shuhua Han, Xinghua Pan, Yueyin Niu, Yun Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title | Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title_full | Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title_fullStr | Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title_full_unstemmed | Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title_short | Expression Patterns of Ezrin and AJAP1 and Clinical Significance in Breast Cancer |
title_sort | expression patterns of ezrin and ajap1 and clinical significance in breast cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931223/ https://www.ncbi.nlm.nih.gov/pubmed/35311087 http://dx.doi.org/10.3389/fonc.2022.831507 |
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