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TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9
Breast cancer is the first killer leading to female death, and tumor metastasis is one of the important factors leading to the death of patients, but the specific mechanism of breast cancer metastasis is not very clear at present. Our study showed that overexpression of TIMELESS could significantly...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798230/ https://www.ncbi.nlm.nih.gov/pubmed/33430865 http://dx.doi.org/10.1186/s12935-021-01752-y |
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author | Li, Bowen Mu, Liying Li, Yanan Xia, Kangkai Yang, Yuxi Aman, Sattout Ahmad, Bashir Li, Shujing Wu, Huijian |
author_facet | Li, Bowen Mu, Liying Li, Yanan Xia, Kangkai Yang, Yuxi Aman, Sattout Ahmad, Bashir Li, Shujing Wu, Huijian |
author_sort | Li, Bowen |
collection | PubMed |
description | Breast cancer is the first killer leading to female death, and tumor metastasis is one of the important factors leading to the death of patients, but the specific mechanism of breast cancer metastasis is not very clear at present. Our study showed that overexpression of TIMELESS could significantly inhibit the invasion and metastasis of breast cancer cells ZR-75-30 and the assembly of F-actin protein. On the contrary, knockdown of TIMELESS promoted the invasion and metastasis of breast cancer cells. Further study revealed that TIMELESS overexpression decreased the mRNA and protein levels of MMP9. Furthermore, TIMELESS could interact with p65, leading to repress the association of p65 and its acetyltransferase CBP and down-regulating the acetylation level of p65, which inhibited the activation of NF-κB signal pathway. In conclusion, our research showed that TIMELESS may repress the invasion and metastasis of breast cancer cells via inhibiting the acetylation of p65, inhibiting the activation of NF-κB, thus down-regulating the expression of MMP9, and then inhibiting the invasion and metastasis of breast cancer cells. |
format | Online Article Text |
id | pubmed-7798230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77982302021-01-11 TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 Li, Bowen Mu, Liying Li, Yanan Xia, Kangkai Yang, Yuxi Aman, Sattout Ahmad, Bashir Li, Shujing Wu, Huijian Cancer Cell Int Primary Research Breast cancer is the first killer leading to female death, and tumor metastasis is one of the important factors leading to the death of patients, but the specific mechanism of breast cancer metastasis is not very clear at present. Our study showed that overexpression of TIMELESS could significantly inhibit the invasion and metastasis of breast cancer cells ZR-75-30 and the assembly of F-actin protein. On the contrary, knockdown of TIMELESS promoted the invasion and metastasis of breast cancer cells. Further study revealed that TIMELESS overexpression decreased the mRNA and protein levels of MMP9. Furthermore, TIMELESS could interact with p65, leading to repress the association of p65 and its acetyltransferase CBP and down-regulating the acetylation level of p65, which inhibited the activation of NF-κB signal pathway. In conclusion, our research showed that TIMELESS may repress the invasion and metastasis of breast cancer cells via inhibiting the acetylation of p65, inhibiting the activation of NF-κB, thus down-regulating the expression of MMP9, and then inhibiting the invasion and metastasis of breast cancer cells. BioMed Central 2021-01-11 /pmc/articles/PMC7798230/ /pubmed/33430865 http://dx.doi.org/10.1186/s12935-021-01752-y Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 | Primary Research Li, Bowen Mu, Liying Li, Yanan Xia, Kangkai Yang, Yuxi Aman, Sattout Ahmad, Bashir Li, Shujing Wu, Huijian TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title | TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title_full | TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title_fullStr | TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title_full_unstemmed | TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title_short | TIMELESS inhibits breast cancer cell invasion and metastasis by down-regulating the expression of MMP9 |
title_sort | timeless inhibits breast cancer cell invasion and metastasis by down-regulating the expression of mmp9 |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798230/ https://www.ncbi.nlm.nih.gov/pubmed/33430865 http://dx.doi.org/10.1186/s12935-021-01752-y |
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