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SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1
Nasopharyngeal carcinoma is a tumor with high malignancy and poor prognosis, which severely affects the health of the patients. LncRNAs and microRNAs are crucial for the occurrence and development of nasopharyngeal carcinoma, which regulate the progression of nasopharyngeal carcinoma through the ceR...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069050/ https://www.ncbi.nlm.nih.gov/pubmed/37009875 http://dx.doi.org/10.1186/s12860-023-00477-2 |
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author | Jiang, Chunmao Feng, Dandan Zhang, Yu Yang, Kun Hu, Xiaotong Xie, Qian |
author_facet | Jiang, Chunmao Feng, Dandan Zhang, Yu Yang, Kun Hu, Xiaotong Xie, Qian |
author_sort | Jiang, Chunmao |
collection | PubMed |
description | Nasopharyngeal carcinoma is a tumor with high malignancy and poor prognosis, which severely affects the health of the patients. LncRNAs and microRNAs are crucial for the occurrence and development of nasopharyngeal carcinoma, which regulate the progression of nasopharyngeal carcinoma through the ceRNA network. SCARB1 plays an essential role in nasopharyngeal carcinoma. However, the mechanism underlying the regulation of SCARB1 in nasopharyngeal carcinoma through non-coding RNAs remains unclear. Our findings indicated that the SCAT8/miR-125b-5p axis promoted the malignant progression of nasopharyngeal carcinoma by driving the expression of SCARB1. Mechanistically, the expression of SCARB1 could be regulated by the lncRNA, SCAT8 and the microRNA, miR-125b-5p. Moreover, as a ceRNA of miR-125b-5p, SCAT8 can not only regulate the expression of SCARB1, but also regulate the malignant progression of nasopharyngeal carcinoma. Notably, our results reveal a novel ceRNA regulatory network in nasopharyngeal carcinoma, which could serve as a potential target for the diagnosis and treatment of nasopharyngeal carcinoma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12860-023-00477-2. |
format | Online Article Text |
id | pubmed-10069050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100690502023-04-04 SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 Jiang, Chunmao Feng, Dandan Zhang, Yu Yang, Kun Hu, Xiaotong Xie, Qian BMC Mol Cell Biol Research Nasopharyngeal carcinoma is a tumor with high malignancy and poor prognosis, which severely affects the health of the patients. LncRNAs and microRNAs are crucial for the occurrence and development of nasopharyngeal carcinoma, which regulate the progression of nasopharyngeal carcinoma through the ceRNA network. SCARB1 plays an essential role in nasopharyngeal carcinoma. However, the mechanism underlying the regulation of SCARB1 in nasopharyngeal carcinoma through non-coding RNAs remains unclear. Our findings indicated that the SCAT8/miR-125b-5p axis promoted the malignant progression of nasopharyngeal carcinoma by driving the expression of SCARB1. Mechanistically, the expression of SCARB1 could be regulated by the lncRNA, SCAT8 and the microRNA, miR-125b-5p. Moreover, as a ceRNA of miR-125b-5p, SCAT8 can not only regulate the expression of SCARB1, but also regulate the malignant progression of nasopharyngeal carcinoma. Notably, our results reveal a novel ceRNA regulatory network in nasopharyngeal carcinoma, which could serve as a potential target for the diagnosis and treatment of nasopharyngeal carcinoma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12860-023-00477-2. BioMed Central 2023-04-03 /pmc/articles/PMC10069050/ /pubmed/37009875 http://dx.doi.org/10.1186/s12860-023-00477-2 Text en © The Author(s) 2023 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 Jiang, Chunmao Feng, Dandan Zhang, Yu Yang, Kun Hu, Xiaotong Xie, Qian SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title | SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title_full | SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title_fullStr | SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title_full_unstemmed | SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title_short | SCAT8/miR-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through SCARB1 |
title_sort | scat8/mir-125b-5p axis triggers malignant progression of nasopharyngeal carcinoma through scarb1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069050/ https://www.ncbi.nlm.nih.gov/pubmed/37009875 http://dx.doi.org/10.1186/s12860-023-00477-2 |
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