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CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer in the world, the 5-year survival rate of patients with HNSCC is still about 50% due to frequent metastasis and recurrence. Circular RNAs (circRNAs) have been characterized as key regulators of gene expression in numerous...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188624/ https://www.ncbi.nlm.nih.gov/pubmed/35690612 http://dx.doi.org/10.1038/s41420-022-01066-6 |
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author | Wei, Zihao Wang, Ying Peng, Jiakuan Li, Honglin Gu, Junjie Ji, Ning Li, Taiwei Zhou, Xikun Zeng, Xin Li, Jing Chen, Qianming |
author_facet | Wei, Zihao Wang, Ying Peng, Jiakuan Li, Honglin Gu, Junjie Ji, Ning Li, Taiwei Zhou, Xikun Zeng, Xin Li, Jing Chen, Qianming |
author_sort | Wei, Zihao |
collection | PubMed |
description | Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer in the world, the 5-year survival rate of patients with HNSCC is still about 50% due to frequent metastasis and recurrence. Circular RNAs (circRNAs) have been characterized as key regulators of gene expression in numerous malignancies. However, the role of circRNA in HNSCC metastasis remains largely unknown. Here, we demonstrated that the circRFWD3 was significantly upregulated in HNSCC tissues and cell lines by circRNA microarray analysis and qPCR. Notably, high expression of circRFWD3 is related to highly aggressive HNSCC cell lines and lymph node metastasis in HNSCC patients. After that, Sanger sequencing, RNase R, and actinomycin D assay were performed to verify the ring structure of circRFWD3. Then functional experiments found it could promote the metastasis of HNSCC cells both in vitro and in vivo. Mechanistically, a dual-luciferase reporter assay, FISH, RIP, RNA pull-down, RNA-seq, and western blot experiments were employed and found that circRFWD3 served as a miRNAs sponge for miR-27a/27b, leading to the upregulation of PPARγ, and then promoted HNSCC metastasis via NF-κB/MMP13 pathway. Finally, ISH and IHC were carried out to determine the expression levels and clinical significances of circRFWD3 and PPARγ in clinical cohorts of HNSCC. According to the analysis results from two independent HNSCC cohorts, upregulated expression of circRFWD3 and PPARγ were positively associated with worse survival in patients with HNSCC. Overall, our results uncover that circRFWD3 acts a critical role in promoting the aggressiveness of HNSCC cells and is a prognostic marker for the disease, indicating that circRFWD3 may act as a potential therapeutic target in HNSCC. |
format | Online Article Text |
id | pubmed-9188624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91886242022-06-13 CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling Wei, Zihao Wang, Ying Peng, Jiakuan Li, Honglin Gu, Junjie Ji, Ning Li, Taiwei Zhou, Xikun Zeng, Xin Li, Jing Chen, Qianming Cell Death Discov Article Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer in the world, the 5-year survival rate of patients with HNSCC is still about 50% due to frequent metastasis and recurrence. Circular RNAs (circRNAs) have been characterized as key regulators of gene expression in numerous malignancies. However, the role of circRNA in HNSCC metastasis remains largely unknown. Here, we demonstrated that the circRFWD3 was significantly upregulated in HNSCC tissues and cell lines by circRNA microarray analysis and qPCR. Notably, high expression of circRFWD3 is related to highly aggressive HNSCC cell lines and lymph node metastasis in HNSCC patients. After that, Sanger sequencing, RNase R, and actinomycin D assay were performed to verify the ring structure of circRFWD3. Then functional experiments found it could promote the metastasis of HNSCC cells both in vitro and in vivo. Mechanistically, a dual-luciferase reporter assay, FISH, RIP, RNA pull-down, RNA-seq, and western blot experiments were employed and found that circRFWD3 served as a miRNAs sponge for miR-27a/27b, leading to the upregulation of PPARγ, and then promoted HNSCC metastasis via NF-κB/MMP13 pathway. Finally, ISH and IHC were carried out to determine the expression levels and clinical significances of circRFWD3 and PPARγ in clinical cohorts of HNSCC. According to the analysis results from two independent HNSCC cohorts, upregulated expression of circRFWD3 and PPARγ were positively associated with worse survival in patients with HNSCC. Overall, our results uncover that circRFWD3 acts a critical role in promoting the aggressiveness of HNSCC cells and is a prognostic marker for the disease, indicating that circRFWD3 may act as a potential therapeutic target in HNSCC. Nature Publishing Group UK 2022-06-11 /pmc/articles/PMC9188624/ /pubmed/35690612 http://dx.doi.org/10.1038/s41420-022-01066-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wei, Zihao Wang, Ying Peng, Jiakuan Li, Honglin Gu, Junjie Ji, Ning Li, Taiwei Zhou, Xikun Zeng, Xin Li, Jing Chen, Qianming CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title | CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title_full | CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title_fullStr | CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title_full_unstemmed | CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title_short | CircRFWD3 promotes HNSCC metastasis by modulating miR-27a/b/PPARγ signaling |
title_sort | circrfwd3 promotes hnscc metastasis by modulating mir-27a/b/pparγ signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188624/ https://www.ncbi.nlm.nih.gov/pubmed/35690612 http://dx.doi.org/10.1038/s41420-022-01066-6 |
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