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MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2
Colon cancer is a malignant tumor that seriously affects human health. Recently, studies revealed that the expression of MTBP enhanced the proliferation and metastasis of many types of cancer cells. And the data also showed that MTBP has the potential to regulate the expression of ZEB2. However, it...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253212/ https://www.ncbi.nlm.nih.gov/pubmed/34262658 http://dx.doi.org/10.1080/19768354.2021.1938218 |
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author | Shayimu, Paerhati Yusufu, Aikeremu Rehemutula, Aizimaiti Redati, Darebai Jiapaer, Rexida Tuerdi, Rousidan |
author_facet | Shayimu, Paerhati Yusufu, Aikeremu Rehemutula, Aizimaiti Redati, Darebai Jiapaer, Rexida Tuerdi, Rousidan |
author_sort | Shayimu, Paerhati |
collection | PubMed |
description | Colon cancer is a malignant tumor that seriously affects human health. Recently, studies revealed that the expression of MTBP enhanced the proliferation and metastasis of many types of cancer cells. And the data also showed that MTBP has the potential to regulate the expression of ZEB2. However, it is unclear whether MTBP can affect the proliferation, migration and invasion of colon cancer cells by modulating the expression of ZEB2. In this study, we established the MTBP overexpression and knockdown colon cancer cells with the transfection. Next, CCK-8 and transwell assays were carried out to determine the changes of the proliferation and invasion of colon cancer cells, respectively. After that, we overexpressed the ZEB2 in these MTBP knockdown colon cancer cells. Finally, the invasion and migration of these cells were detected with the same methods. We revealed that overexpression of MTBP enhanced the proliferation and invasion of colon cancer cells. Moreover, suppression of MTBP repressed the proliferation, migration and invasion of colon cancer cells. Furthermore, MTBP promoted the expression of ZEB2. The overexpression of ZEB2 abolished the MTBP knockdown induced inhibition of the migration and invasion of colon cancer cells. These results implied that MTBP enhanced the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2. |
format | Online Article Text |
id | pubmed-8253212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-82532122021-07-13 MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 Shayimu, Paerhati Yusufu, Aikeremu Rehemutula, Aizimaiti Redati, Darebai Jiapaer, Rexida Tuerdi, Rousidan Anim Cells Syst (Seoul) Physiology & Biochemistry Colon cancer is a malignant tumor that seriously affects human health. Recently, studies revealed that the expression of MTBP enhanced the proliferation and metastasis of many types of cancer cells. And the data also showed that MTBP has the potential to regulate the expression of ZEB2. However, it is unclear whether MTBP can affect the proliferation, migration and invasion of colon cancer cells by modulating the expression of ZEB2. In this study, we established the MTBP overexpression and knockdown colon cancer cells with the transfection. Next, CCK-8 and transwell assays were carried out to determine the changes of the proliferation and invasion of colon cancer cells, respectively. After that, we overexpressed the ZEB2 in these MTBP knockdown colon cancer cells. Finally, the invasion and migration of these cells were detected with the same methods. We revealed that overexpression of MTBP enhanced the proliferation and invasion of colon cancer cells. Moreover, suppression of MTBP repressed the proliferation, migration and invasion of colon cancer cells. Furthermore, MTBP promoted the expression of ZEB2. The overexpression of ZEB2 abolished the MTBP knockdown induced inhibition of the migration and invasion of colon cancer cells. These results implied that MTBP enhanced the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2. Taylor & Francis 2021-06-15 /pmc/articles/PMC8253212/ /pubmed/34262658 http://dx.doi.org/10.1080/19768354.2021.1938218 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Physiology & Biochemistry Shayimu, Paerhati Yusufu, Aikeremu Rehemutula, Aizimaiti Redati, Darebai Jiapaer, Rexida Tuerdi, Rousidan MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title | MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title_full | MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title_fullStr | MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title_full_unstemmed | MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title_short | MTBP promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of ZEB2 |
title_sort | mtbp promoted the proliferation, migration and invasion of colon cancer cells by activating the expression of zeb2 |
topic | Physiology & Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253212/ https://www.ncbi.nlm.nih.gov/pubmed/34262658 http://dx.doi.org/10.1080/19768354.2021.1938218 |
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