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ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer

BACKGROUND: Histological grade has been demonstrated to be an important factor of breast cancer outcome and is associated with cell differentiation and is currently being evaluated via H&E-stained sections. Molecular biomarkers are essential to improve the accuracy of histological grading. ATBF1...

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Autores principales: Li, Mei, Zheng, Yanan, Li, Xujun, Shen, Xiaohan, Zhang, Tingxia, Weng, Bowen, Mao, Haijiao, Zhao, Jiyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727999/
https://www.ncbi.nlm.nih.gov/pubmed/36476423
http://dx.doi.org/10.1186/s12885-022-10380-2
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author Li, Mei
Zheng, Yanan
Li, Xujun
Shen, Xiaohan
Zhang, Tingxia
Weng, Bowen
Mao, Haijiao
Zhao, Jiyuan
author_facet Li, Mei
Zheng, Yanan
Li, Xujun
Shen, Xiaohan
Zhang, Tingxia
Weng, Bowen
Mao, Haijiao
Zhao, Jiyuan
author_sort Li, Mei
collection PubMed
description BACKGROUND: Histological grade has been demonstrated to be an important factor of breast cancer outcome and is associated with cell differentiation and is currently being evaluated via H&E-stained sections. Molecular biomarkers are essential to improve the accuracy of histological grading. ATBF1, a large transcription factor, has been considered a tumor suppressor gene with frequent mutations or deletions in multiple cancers. In breast cancer, ATBF1 was reported to function in cell differentiation and mammary development. However, its role in the clinic has rarely been reported. METHODS: Breast cancer tissues (BCTs) and adjacent noncancerous tissues (ANCTs) were collected to analyze the expression of ATBF1 at the mRNA and protein levels. Three anti-ATBF1 antibodies recognizing independent peptides of ATBF1 (N-terminal end, middle region and C-terminal end) were applied for IHC staining. Small interfering RNA (siRNA) was used to silence ATBF1 expression and to investigate the roles of ATBF1 in MCF7 cells. Microarrays were introduced to analyze the differentially expressed genes, enriched GO terms and KEGG terms regulated by ATBF1 and its potential downstream genes, which were further confirmed in vitro and in clinical samples. RESULTS: The expression of ATBF1 was reduced in BCTs at both the mRNA and protein levels compared with that in ANCTs. ATBF1 protein was predominantly localized in the nucleus of ANCTs but in the cytoplasm of BCTs. Both the mRNA and protein levels of ATBF1 were significantly correlated with histological grade. Consistently, knockdown of ATBF1 increased stemness marker expression and reduced differentiation markers in vitro. Further analysis identified WNT5A as an essential downstream gene of ATBF1 in breast cancer cells. Treatment of WNT5A disrupted cell proliferation induced by ATBF1 silencing. In BCTs, a significant correlation was observed between the expression of WNT5A and ATBF1. CONCLUSION: The results indicated that ATBF1 expression might be a useful diagnostic marker associated with histological grade and breast cancer malignancy. WNT5A and its signaling pathway are novel mechanisms by which ATBF1 contributes to breast cancer tumorigenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10380-2.
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spelling pubmed-97279992022-12-08 ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer Li, Mei Zheng, Yanan Li, Xujun Shen, Xiaohan Zhang, Tingxia Weng, Bowen Mao, Haijiao Zhao, Jiyuan BMC Cancer Research BACKGROUND: Histological grade has been demonstrated to be an important factor of breast cancer outcome and is associated with cell differentiation and is currently being evaluated via H&E-stained sections. Molecular biomarkers are essential to improve the accuracy of histological grading. ATBF1, a large transcription factor, has been considered a tumor suppressor gene with frequent mutations or deletions in multiple cancers. In breast cancer, ATBF1 was reported to function in cell differentiation and mammary development. However, its role in the clinic has rarely been reported. METHODS: Breast cancer tissues (BCTs) and adjacent noncancerous tissues (ANCTs) were collected to analyze the expression of ATBF1 at the mRNA and protein levels. Three anti-ATBF1 antibodies recognizing independent peptides of ATBF1 (N-terminal end, middle region and C-terminal end) were applied for IHC staining. Small interfering RNA (siRNA) was used to silence ATBF1 expression and to investigate the roles of ATBF1 in MCF7 cells. Microarrays were introduced to analyze the differentially expressed genes, enriched GO terms and KEGG terms regulated by ATBF1 and its potential downstream genes, which were further confirmed in vitro and in clinical samples. RESULTS: The expression of ATBF1 was reduced in BCTs at both the mRNA and protein levels compared with that in ANCTs. ATBF1 protein was predominantly localized in the nucleus of ANCTs but in the cytoplasm of BCTs. Both the mRNA and protein levels of ATBF1 were significantly correlated with histological grade. Consistently, knockdown of ATBF1 increased stemness marker expression and reduced differentiation markers in vitro. Further analysis identified WNT5A as an essential downstream gene of ATBF1 in breast cancer cells. Treatment of WNT5A disrupted cell proliferation induced by ATBF1 silencing. In BCTs, a significant correlation was observed between the expression of WNT5A and ATBF1. CONCLUSION: The results indicated that ATBF1 expression might be a useful diagnostic marker associated with histological grade and breast cancer malignancy. WNT5A and its signaling pathway are novel mechanisms by which ATBF1 contributes to breast cancer tumorigenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10380-2. BioMed Central 2022-12-07 /pmc/articles/PMC9727999/ /pubmed/36476423 http://dx.doi.org/10.1186/s12885-022-10380-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Mei
Zheng, Yanan
Li, Xujun
Shen, Xiaohan
Zhang, Tingxia
Weng, Bowen
Mao, Haijiao
Zhao, Jiyuan
ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title_full ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title_fullStr ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title_full_unstemmed ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title_short ATBF1 is a potential diagnostic marker of histological grade and functions via WNT5A in breast cancer
title_sort atbf1 is a potential diagnostic marker of histological grade and functions via wnt5a in breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727999/
https://www.ncbi.nlm.nih.gov/pubmed/36476423
http://dx.doi.org/10.1186/s12885-022-10380-2
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