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Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development
Circular RNA (circRNA) is a type of noncoding RNA that can interact with miRNAs to regulate gene expression. However, little is known concerning circRNA, which is crucial in the pathogenesis of lung cancer. To date, limited studies have explored the role of circ_0044516 in lung cancer progression. R...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253637/ https://www.ncbi.nlm.nih.gov/pubmed/34258296 http://dx.doi.org/10.1155/2021/5510869 |
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author | Chen, Yue-Wei Du, Qiu-Rong He, Yu-Juan Chen, Wen-Shu Jiang, Wen-Yang Gui, Qi Xu, Cheng-Cheng Wang, Wei Cheng, Hong-Yun |
author_facet | Chen, Yue-Wei Du, Qiu-Rong He, Yu-Juan Chen, Wen-Shu Jiang, Wen-Yang Gui, Qi Xu, Cheng-Cheng Wang, Wei Cheng, Hong-Yun |
author_sort | Chen, Yue-Wei |
collection | PubMed |
description | Circular RNA (circRNA) is a type of noncoding RNA that can interact with miRNAs to regulate gene expression. However, little is known concerning circRNA, which is crucial in the pathogenesis of lung cancer. To date, limited studies have explored the role of circ_0044516 in lung cancer progression. Recently, we observed that circ_0044516 expression levels were obviously elevated in lung cancer tissues and cells. A549 and SPCA1 cells were transfected with circ_0044516 siRNA. We observed that knockdown of circ_0044516 dramatically repressed cell proliferation, increased cell apoptosis, and repressed the cell cycle. Moreover, A549 and SPCA1 cell migration and invasion abilities were greatly repressed by circ_0044516 siRNA. Due to accumulating evidence demonstrating the vital role of cancer stem cells, their mechanism of involvement has drawn increasing attention in tumor progression and metastasis research. We also found that cancer stem cell properties were restrained by silencing circ_0044516 in A549 and SPC-A1 cells. Moreover, in vivo xenograft experiments showed that circ_0044516 downregulation reduced tumor growth. Mechanistically, in lung cancer and using bioinformatics, we demonstrated that circ_0044516 sponges miR-136 targeting MAT2A. Furthermore, rescue assays were carried out to identify that circ_0044516 modulates cell proliferation, invasion, and stemness by regulating miR-136 and MAT2A in lung cancer. In summary, our study revealed that the circ_0044516/miR-136/MAT2A axis is involved in lung cancer progression. Our findings may provide novel targets for diagnosis and therapeutic intervention in lung cancer patients. |
format | Online Article Text |
id | pubmed-8253637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-82536372021-07-12 Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development Chen, Yue-Wei Du, Qiu-Rong He, Yu-Juan Chen, Wen-Shu Jiang, Wen-Yang Gui, Qi Xu, Cheng-Cheng Wang, Wei Cheng, Hong-Yun J Immunol Res Research Article Circular RNA (circRNA) is a type of noncoding RNA that can interact with miRNAs to regulate gene expression. However, little is known concerning circRNA, which is crucial in the pathogenesis of lung cancer. To date, limited studies have explored the role of circ_0044516 in lung cancer progression. Recently, we observed that circ_0044516 expression levels were obviously elevated in lung cancer tissues and cells. A549 and SPCA1 cells were transfected with circ_0044516 siRNA. We observed that knockdown of circ_0044516 dramatically repressed cell proliferation, increased cell apoptosis, and repressed the cell cycle. Moreover, A549 and SPCA1 cell migration and invasion abilities were greatly repressed by circ_0044516 siRNA. Due to accumulating evidence demonstrating the vital role of cancer stem cells, their mechanism of involvement has drawn increasing attention in tumor progression and metastasis research. We also found that cancer stem cell properties were restrained by silencing circ_0044516 in A549 and SPC-A1 cells. Moreover, in vivo xenograft experiments showed that circ_0044516 downregulation reduced tumor growth. Mechanistically, in lung cancer and using bioinformatics, we demonstrated that circ_0044516 sponges miR-136 targeting MAT2A. Furthermore, rescue assays were carried out to identify that circ_0044516 modulates cell proliferation, invasion, and stemness by regulating miR-136 and MAT2A in lung cancer. In summary, our study revealed that the circ_0044516/miR-136/MAT2A axis is involved in lung cancer progression. Our findings may provide novel targets for diagnosis and therapeutic intervention in lung cancer patients. Hindawi 2021-06-24 /pmc/articles/PMC8253637/ /pubmed/34258296 http://dx.doi.org/10.1155/2021/5510869 Text en Copyright © 2021 Yue-Wei Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Yue-Wei Du, Qiu-Rong He, Yu-Juan Chen, Wen-Shu Jiang, Wen-Yang Gui, Qi Xu, Cheng-Cheng Wang, Wei Cheng, Hong-Yun Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title | Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title_full | Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title_fullStr | Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title_full_unstemmed | Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title_short | Circ_0044516 Regulates miR-136/MAT2A Pathway to Facilitate Lung Cancer Development |
title_sort | circ_0044516 regulates mir-136/mat2a pathway to facilitate lung cancer development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253637/ https://www.ncbi.nlm.nih.gov/pubmed/34258296 http://dx.doi.org/10.1155/2021/5510869 |
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