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Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15

OBJECTIVES: Circular RNAs (circRNAs) are a subclass of noncoding RNAs, playing essential roles in tumorigenesis and aggressiveness. Recent studies have revealed the pivotal functions of circ‐CTNNB1 (a circular RNA derived from CTNNB1) in cancer progression. However, little is known about the role of...

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Autores principales: Yang, Feng, Liu, Yangyang, Xiao, Jun, Li, Bo, Chen, Yajun, Hu, Anpei, Zeng, Jin, Liu, Zhili, Liu, Hucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816931/
https://www.ncbi.nlm.nih.gov/pubmed/36181462
http://dx.doi.org/10.1111/cpr.13344
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author Yang, Feng
Liu, Yangyang
Xiao, Jun
Li, Bo
Chen, Yajun
Hu, Anpei
Zeng, Jin
Liu, Zhili
Liu, Hucheng
author_facet Yang, Feng
Liu, Yangyang
Xiao, Jun
Li, Bo
Chen, Yajun
Hu, Anpei
Zeng, Jin
Liu, Zhili
Liu, Hucheng
author_sort Yang, Feng
collection PubMed
description OBJECTIVES: Circular RNAs (circRNAs) are a subclass of noncoding RNAs, playing essential roles in tumorigenesis and aggressiveness. Recent studies have revealed the pivotal functions of circ‐CTNNB1 (a circular RNA derived from CTNNB1) in cancer progression. However, little is known about the role of circ‐CTNNB1 in osteosarcoma (OS), a highly malignant bone tumour in children and adolescents. METHODS: Circ‐CTNNB1 was analysed by qRT‐PCR, and the results were confirmed by Sanger sequencing. The interaction and effects between circ‐CTNNB1 and RNA binding motif protein 15 (RBM15) were analysed through biotin‐labelled RNA pull‐down and mass spectrometry, in vitro binding, and RNA electrophoretic mobility shift assays. In vitro and in vivo experiments were performed to evaluate the biological functions and underlying mechanisms of circ‐CTNNB1 and RBM15 in OS cells. RESULTS: Circ‐CTNNB1 was highly expressed in OS tissues and predominantly detected in the nucleus of OS cells. Ectopic expression of circ‐CTNNB1 promoted the growth, invasion, and metastasis of OS cells in vitro and in vivo. Mechanistically, circ‐CTNNB1 interacted with RBM15 and subsequently promoted the expression of hexokinase 2 (HK2), glucose‐6‐phosphate isomerase (GPI) and phosphoglycerate kinase 1 (PGK1) through N6‐methyladenosine (m6A) modification to facilitate the glycolysis process and activate OS progression. CONCLUSIONS: Circ‐CTNNB1 drives aerobic glycolysis and OS progression by facilitating RBM15‐mediated m6A modification.
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spelling pubmed-98169312023-01-06 Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15 Yang, Feng Liu, Yangyang Xiao, Jun Li, Bo Chen, Yajun Hu, Anpei Zeng, Jin Liu, Zhili Liu, Hucheng Cell Prolif Original Articles OBJECTIVES: Circular RNAs (circRNAs) are a subclass of noncoding RNAs, playing essential roles in tumorigenesis and aggressiveness. Recent studies have revealed the pivotal functions of circ‐CTNNB1 (a circular RNA derived from CTNNB1) in cancer progression. However, little is known about the role of circ‐CTNNB1 in osteosarcoma (OS), a highly malignant bone tumour in children and adolescents. METHODS: Circ‐CTNNB1 was analysed by qRT‐PCR, and the results were confirmed by Sanger sequencing. The interaction and effects between circ‐CTNNB1 and RNA binding motif protein 15 (RBM15) were analysed through biotin‐labelled RNA pull‐down and mass spectrometry, in vitro binding, and RNA electrophoretic mobility shift assays. In vitro and in vivo experiments were performed to evaluate the biological functions and underlying mechanisms of circ‐CTNNB1 and RBM15 in OS cells. RESULTS: Circ‐CTNNB1 was highly expressed in OS tissues and predominantly detected in the nucleus of OS cells. Ectopic expression of circ‐CTNNB1 promoted the growth, invasion, and metastasis of OS cells in vitro and in vivo. Mechanistically, circ‐CTNNB1 interacted with RBM15 and subsequently promoted the expression of hexokinase 2 (HK2), glucose‐6‐phosphate isomerase (GPI) and phosphoglycerate kinase 1 (PGK1) through N6‐methyladenosine (m6A) modification to facilitate the glycolysis process and activate OS progression. CONCLUSIONS: Circ‐CTNNB1 drives aerobic glycolysis and OS progression by facilitating RBM15‐mediated m6A modification. John Wiley and Sons Inc. 2022-10-01 /pmc/articles/PMC9816931/ /pubmed/36181462 http://dx.doi.org/10.1111/cpr.13344 Text en © 2022 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yang, Feng
Liu, Yangyang
Xiao, Jun
Li, Bo
Chen, Yajun
Hu, Anpei
Zeng, Jin
Liu, Zhili
Liu, Hucheng
Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title_full Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title_fullStr Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title_full_unstemmed Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title_short Circ‐CTNNB1 drives aerobic glycolysis and osteosarcoma progression via m6A modification through interacting with RBM15
title_sort circ‐ctnnb1 drives aerobic glycolysis and osteosarcoma progression via m6a modification through interacting with rbm15
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816931/
https://www.ncbi.nlm.nih.gov/pubmed/36181462
http://dx.doi.org/10.1111/cpr.13344
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