Cargando…

HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer

Triple-negative breast cancer (TNBC) is the most malignant subtype of breast cancer. In the absence of effective molecular markers for TNBC, there is an urgent clinical need for promising therapeutic target for TNBC. Histone deacetylases (HDACs), key regulators for chromatin remodeling and gene expr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Mengdi, Liu, Nianqiu, Lin, Jinna, Wang, Jingru, Lai, Hongna, Liu, Yujie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773322/
https://www.ncbi.nlm.nih.gov/pubmed/36589669
http://dx.doi.org/10.3892/ol.2022.13619
_version_ 1784855170219245568
author Zhu, Mengdi
Liu, Nianqiu
Lin, Jinna
Wang, Jingru
Lai, Hongna
Liu, Yujie
author_facet Zhu, Mengdi
Liu, Nianqiu
Lin, Jinna
Wang, Jingru
Lai, Hongna
Liu, Yujie
author_sort Zhu, Mengdi
collection PubMed
description Triple-negative breast cancer (TNBC) is the most malignant subtype of breast cancer. In the absence of effective molecular markers for TNBC, there is an urgent clinical need for promising therapeutic target for TNBC. Histone deacetylases (HDACs), key regulators for chromatin remodeling and gene expression, have been suggested to play critical roles in cancer development. However, little is known ~the functions and implications of HDACs in TNBC treatment in the future. By analyzing the expression and prognostic significance of HDAC family members in TNBC through TCGA and METABRIC databases, HDAC7 was found to be downregulated in TNBC samples and the survival of patients with lower expression of HDAC7 was shorter. Furthermore, HDAC7 was negatively associated with NudC domain containing 1 (NudCD1) and γ-glutamyl hydrolase (GGH). Loss of NudCD1 or GGH predicted improved overall survival time (OS) of patients with TNBC. In vitro experiments showed that silencing of HDAC7 enhanced TNBC cell proliferation, while overexpression HDAC7 inhibited TNBC cell proliferation. The results of functional experiments confirmed that HDAC7 negatively modulated GGH and NudCD1 expression. Furthermore, decrease of NudCD1 or GGH inhibited cell proliferation. Notably, the HDAC7-NudCD1/GGH axis was found to be associated with NK cell infiltration. Overall, the present study revealed a novel role of HDAC7-NudCD1/GGH axis in TNBC, which might provide a promising treatment strategy for patients with TNBC.
format Online
Article
Text
id pubmed-9773322
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-97733222022-12-29 HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer Zhu, Mengdi Liu, Nianqiu Lin, Jinna Wang, Jingru Lai, Hongna Liu, Yujie Oncol Lett Articles Triple-negative breast cancer (TNBC) is the most malignant subtype of breast cancer. In the absence of effective molecular markers for TNBC, there is an urgent clinical need for promising therapeutic target for TNBC. Histone deacetylases (HDACs), key regulators for chromatin remodeling and gene expression, have been suggested to play critical roles in cancer development. However, little is known ~the functions and implications of HDACs in TNBC treatment in the future. By analyzing the expression and prognostic significance of HDAC family members in TNBC through TCGA and METABRIC databases, HDAC7 was found to be downregulated in TNBC samples and the survival of patients with lower expression of HDAC7 was shorter. Furthermore, HDAC7 was negatively associated with NudC domain containing 1 (NudCD1) and γ-glutamyl hydrolase (GGH). Loss of NudCD1 or GGH predicted improved overall survival time (OS) of patients with TNBC. In vitro experiments showed that silencing of HDAC7 enhanced TNBC cell proliferation, while overexpression HDAC7 inhibited TNBC cell proliferation. The results of functional experiments confirmed that HDAC7 negatively modulated GGH and NudCD1 expression. Furthermore, decrease of NudCD1 or GGH inhibited cell proliferation. Notably, the HDAC7-NudCD1/GGH axis was found to be associated with NK cell infiltration. Overall, the present study revealed a novel role of HDAC7-NudCD1/GGH axis in TNBC, which might provide a promising treatment strategy for patients with TNBC. D.A. Spandidos 2022-12-05 /pmc/articles/PMC9773322/ /pubmed/36589669 http://dx.doi.org/10.3892/ol.2022.13619 Text en Copyright: © Zhu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhu, Mengdi
Liu, Nianqiu
Lin, Jinna
Wang, Jingru
Lai, Hongna
Liu, Yujie
HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title_full HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title_fullStr HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title_full_unstemmed HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title_short HDAC7 inhibits cell proliferation via NudCD1/GGH axis in triple-negative breast cancer
title_sort hdac7 inhibits cell proliferation via nudcd1/ggh axis in triple-negative breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773322/
https://www.ncbi.nlm.nih.gov/pubmed/36589669
http://dx.doi.org/10.3892/ol.2022.13619
work_keys_str_mv AT zhumengdi hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer
AT liunianqiu hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer
AT linjinna hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer
AT wangjingru hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer
AT laihongna hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer
AT liuyujie hdac7inhibitscellproliferationvianudcd1gghaxisintriplenegativebreastcancer