Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Zihao, Wang, Ying, Peng, Jiakuan, Li, Honglin, Gu, Junjie, Ji, Ning, Li, Taiwei, Zhou, Xikun, Zeng, Xin, Li, Jing, Chen, Qianming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784725413049663488
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
work_keys_str_mv AT weizihao circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT wangying circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT pengjiakuan circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT lihonglin circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT gujunjie circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT jining circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT litaiwei circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT zhouxikun circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT zengxin circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT lijing circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling
AT chenqianming circrfwd3promoteshnsccmetastasisbymodulatingmir27abppargsignaling