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Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2
Breast cancer is the most common female cancer in the world. Despite the active research on metastatic breast cancer, the treatment of breast cancer patients is still difficult because the mechanism is not well known. Therefore, research on new targets and mechanisms for diagnosis and treatment of b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365326/ https://www.ncbi.nlm.nih.gov/pubmed/34457998 http://dx.doi.org/10.1016/j.omtn.2021.05.004 |
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author | Seok, Hyun Jeong Choi, Young Eun Choi, Jae Yeon Yi, Joo Mi Kim, Eun Joo Choi, Mi Young Lee, Su-Jae Bae, In Hwa |
author_facet | Seok, Hyun Jeong Choi, Young Eun Choi, Jae Yeon Yi, Joo Mi Kim, Eun Joo Choi, Mi Young Lee, Su-Jae Bae, In Hwa |
author_sort | Seok, Hyun Jeong |
collection | PubMed |
description | Breast cancer is the most common female cancer in the world. Despite the active research on metastatic breast cancer, the treatment of breast cancer patients is still difficult because the mechanism is not well known. Therefore, research on new targets and mechanisms for diagnosis and treatment of breast cancer patients is required. On the other hand, microRNA (miRNA) has the advantage of simultaneously regulating the expression of many target genes, so it has been proposed as an effective biomarker for the treatment of various diseases including cancer. This study analyzed the role and mechanism of DBC2 (deleted in breast cancer 2), which is known to inhibit its expression in breast cancer, and proposed microRNA (miR)-5088-5p, which regulates its expression. It was revealed that the biogenesis of miR-5088-5p was upregulated by hypomethylation of its promoter, promoted by Fyn, and was involved in malignancy in breast cancer. With the use of the cellular level, clinical samples, and published data, we verified that the expression patterns of DBC2 and miR-5088-5p were negatively related, suggesting the potential as novel biomarkers for the diagnosis of breast cancer patients. |
format | Online Article Text |
id | pubmed-8365326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-83653262021-08-27 Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 Seok, Hyun Jeong Choi, Young Eun Choi, Jae Yeon Yi, Joo Mi Kim, Eun Joo Choi, Mi Young Lee, Su-Jae Bae, In Hwa Mol Ther Nucleic Acids Original Article Breast cancer is the most common female cancer in the world. Despite the active research on metastatic breast cancer, the treatment of breast cancer patients is still difficult because the mechanism is not well known. Therefore, research on new targets and mechanisms for diagnosis and treatment of breast cancer patients is required. On the other hand, microRNA (miRNA) has the advantage of simultaneously regulating the expression of many target genes, so it has been proposed as an effective biomarker for the treatment of various diseases including cancer. This study analyzed the role and mechanism of DBC2 (deleted in breast cancer 2), which is known to inhibit its expression in breast cancer, and proposed microRNA (miR)-5088-5p, which regulates its expression. It was revealed that the biogenesis of miR-5088-5p was upregulated by hypomethylation of its promoter, promoted by Fyn, and was involved in malignancy in breast cancer. With the use of the cellular level, clinical samples, and published data, we verified that the expression patterns of DBC2 and miR-5088-5p were negatively related, suggesting the potential as novel biomarkers for the diagnosis of breast cancer patients. American Society of Gene & Cell Therapy 2021-05-08 /pmc/articles/PMC8365326/ /pubmed/34457998 http://dx.doi.org/10.1016/j.omtn.2021.05.004 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Seok, Hyun Jeong Choi, Young Eun Choi, Jae Yeon Yi, Joo Mi Kim, Eun Joo Choi, Mi Young Lee, Su-Jae Bae, In Hwa Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title | Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title_full | Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title_fullStr | Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title_full_unstemmed | Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title_short | Novel miR-5088-5p promotes malignancy of breast cancer by inhibiting DBC2 |
title_sort | novel mir-5088-5p promotes malignancy of breast cancer by inhibiting dbc2 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365326/ https://www.ncbi.nlm.nih.gov/pubmed/34457998 http://dx.doi.org/10.1016/j.omtn.2021.05.004 |
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