Cargando…

circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop

BACKGROUND: In recent years, an increasing number of studies have indicated that circular RNA plays crucial roles in regulating tumor development and chemoresistance. Using two high-throughput RNA sequence datasets, we previously found that circEXOC6B was downregulated in colon cancer. However, its...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xiaomin, Wang, Jianjun, Lin, Weihao, Yuan, Qinzi, Lu, Yanxia, Wang, Haowei, Chen, Yujia, Chen, Lixia, Dai, Peiling, Long, Huaicheng, Li, Xuenong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219196/
https://www.ncbi.nlm.nih.gov/pubmed/35739524
http://dx.doi.org/10.1186/s12943-022-01600-1
_version_ 1784732060480438272
author Li, Xiaomin
Wang, Jianjun
Lin, Weihao
Yuan, Qinzi
Lu, Yanxia
Wang, Haowei
Chen, Yujia
Chen, Lixia
Dai, Peiling
Long, Huaicheng
Li, Xuenong
author_facet Li, Xiaomin
Wang, Jianjun
Lin, Weihao
Yuan, Qinzi
Lu, Yanxia
Wang, Haowei
Chen, Yujia
Chen, Lixia
Dai, Peiling
Long, Huaicheng
Li, Xuenong
author_sort Li, Xiaomin
collection PubMed
description BACKGROUND: In recent years, an increasing number of studies have indicated that circular RNA plays crucial roles in regulating tumor development and chemoresistance. Using two high-throughput RNA sequence datasets, we previously found that circEXOC6B was downregulated in colon cancer. However, its role and mechanism in colorectal cancer (CRC) remained unknown. METHODS: Real-time quantitative PCR was used to examine the expression of circEXOC6B in CRC tissues. In vivo and in vitro functional experiments were performed to determine the suppressor role of circEXOC6B in CRC progression. RNA pull-down, mass spectrometry, RNA-binding protein immunoprecipitation, co-immunoprecipitation, fluorescence in situ hybridization, and immunofluorescence were applied to investigate the possible mechanisms connecting circEXOC6B to CRC growth and 5-fluorouracil-induced apoptosis. Chromatin immunoprecipitation, dual-luciferase assay, western blot, and immunohistochemistry were used to explore the mechanisms underlying the HIF1A regulation of RRAGB transcription. RESULTS: circEXOC6B was downregulated in CRC tissues, and its lower expression was associated with poor prognosis of patients. Functional experiments showed that circEXOC6B inhibited growth and increased the 5-fluorouracil-induced apoptosis of CRC cells in vitro and in vivo. Mechanistically, circEXOC6B inhibited the heterodimer formation of RRAGB by binding to it, thereby suppressing the mTORC1 pathway and HIF1A level. In addition, HIF1A upregulated the transcription of RRAGB by binding to its promoter region. Altogether, the results demonstrated that a HIF1A-RRAGB-mTORC1 positive feedback loop drives tumor progression in CRC, which could be interrupted by circEXOC6B. CONCLUSIONS: circEXOC6B inhibits the progression of CRC and enhances the chemosensitivity of CRC cells to 5-fluorouracil by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop. circEXOC6B is a possible therapeutic target for CRC treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-022-01600-1.
format Online
Article
Text
id pubmed-9219196
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-92191962022-06-24 circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop Li, Xiaomin Wang, Jianjun Lin, Weihao Yuan, Qinzi Lu, Yanxia Wang, Haowei Chen, Yujia Chen, Lixia Dai, Peiling Long, Huaicheng Li, Xuenong Mol Cancer Research BACKGROUND: In recent years, an increasing number of studies have indicated that circular RNA plays crucial roles in regulating tumor development and chemoresistance. Using two high-throughput RNA sequence datasets, we previously found that circEXOC6B was downregulated in colon cancer. However, its role and mechanism in colorectal cancer (CRC) remained unknown. METHODS: Real-time quantitative PCR was used to examine the expression of circEXOC6B in CRC tissues. In vivo and in vitro functional experiments were performed to determine the suppressor role of circEXOC6B in CRC progression. RNA pull-down, mass spectrometry, RNA-binding protein immunoprecipitation, co-immunoprecipitation, fluorescence in situ hybridization, and immunofluorescence were applied to investigate the possible mechanisms connecting circEXOC6B to CRC growth and 5-fluorouracil-induced apoptosis. Chromatin immunoprecipitation, dual-luciferase assay, western blot, and immunohistochemistry were used to explore the mechanisms underlying the HIF1A regulation of RRAGB transcription. RESULTS: circEXOC6B was downregulated in CRC tissues, and its lower expression was associated with poor prognosis of patients. Functional experiments showed that circEXOC6B inhibited growth and increased the 5-fluorouracil-induced apoptosis of CRC cells in vitro and in vivo. Mechanistically, circEXOC6B inhibited the heterodimer formation of RRAGB by binding to it, thereby suppressing the mTORC1 pathway and HIF1A level. In addition, HIF1A upregulated the transcription of RRAGB by binding to its promoter region. Altogether, the results demonstrated that a HIF1A-RRAGB-mTORC1 positive feedback loop drives tumor progression in CRC, which could be interrupted by circEXOC6B. CONCLUSIONS: circEXOC6B inhibits the progression of CRC and enhances the chemosensitivity of CRC cells to 5-fluorouracil by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop. circEXOC6B is a possible therapeutic target for CRC treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-022-01600-1. BioMed Central 2022-06-23 /pmc/articles/PMC9219196/ /pubmed/35739524 http://dx.doi.org/10.1186/s12943-022-01600-1 Text en © The Author(s) 2022 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
Li, Xiaomin
Wang, Jianjun
Lin, Weihao
Yuan, Qinzi
Lu, Yanxia
Wang, Haowei
Chen, Yujia
Chen, Lixia
Dai, Peiling
Long, Huaicheng
Li, Xuenong
circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title_full circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title_fullStr circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title_full_unstemmed circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title_short circEXOC6B interacting with RRAGB, an mTORC1 activator, inhibits the progression of colorectal cancer by antagonizing the HIF1A-RRAGB-mTORC1 positive feedback loop
title_sort circexoc6b interacting with rragb, an mtorc1 activator, inhibits the progression of colorectal cancer by antagonizing the hif1a-rragb-mtorc1 positive feedback loop
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219196/
https://www.ncbi.nlm.nih.gov/pubmed/35739524
http://dx.doi.org/10.1186/s12943-022-01600-1
work_keys_str_mv AT lixiaomin circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT wangjianjun circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT linweihao circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT yuanqinzi circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT luyanxia circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT wanghaowei circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT chenyujia circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT chenlixia circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT daipeiling circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT longhuaicheng circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop
AT lixuenong circexoc6binteractingwithrragbanmtorc1activatorinhibitstheprogressionofcolorectalcancerbyantagonizingthehif1arragbmtorc1positivefeedbackloop