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Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis

Circular RNAs (circRNAs) are a distinct class of non-coding RNAs that play regulatory roles in the initiation and progression of tumors. With advancements in transcriptome sequencing technology, numerous circRNAs that play significant roles in tumor-related genes have been identified. In this study,...

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Autores principales: Yu, Jin-hao, Tan, Jia-nan, Zhong, Guang-yu, Zhong, Lin, Hou, Dong, Ma, Shuai, Wang, Peng-liang, Zhang, Zhi-hong, Lu, Xu-qiang, Yang, Bin, Zhou, Sheng-ning, Han, Fang-hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652212/
https://www.ncbi.nlm.nih.gov/pubmed/37925795
http://dx.doi.org/10.1016/j.tranon.2023.101823
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author Yu, Jin-hao
Tan, Jia-nan
Zhong, Guang-yu
Zhong, Lin
Hou, Dong
Ma, Shuai
Wang, Peng-liang
Zhang, Zhi-hong
Lu, Xu-qiang
Yang, Bin
Zhou, Sheng-ning
Han, Fang-hai
author_facet Yu, Jin-hao
Tan, Jia-nan
Zhong, Guang-yu
Zhong, Lin
Hou, Dong
Ma, Shuai
Wang, Peng-liang
Zhang, Zhi-hong
Lu, Xu-qiang
Yang, Bin
Zhou, Sheng-ning
Han, Fang-hai
author_sort Yu, Jin-hao
collection PubMed
description Circular RNAs (circRNAs) are a distinct class of non-coding RNAs that play regulatory roles in the initiation and progression of tumors. With advancements in transcriptome sequencing technology, numerous circRNAs that play significant roles in tumor-related genes have been identified. In this study, we used transcriptome sequencing to analyze the expression levels of circRNAs in normal adjacent tissues, primary colorectal cancer (CRC) tissues, and CRC tissues with liver metastasis. We successfully identified the circRNA hsa_circ_0020134 (circ0020134), which exhibited significantly elevated expression specifically in CRC with liver metastasis. Importantly, high levels of circ0020134 were associated with a poor prognosis among patients. Functional experiments demonstrated that circ0020134 promotes the proliferation and metastasis of CRC cells both in vitro and in vivo. Mechanistically, upregulation of circ0020134 was induced by the transcription factor, PAX5, while miR-183-5p acted as a sponge for circ0020134, leading to partial upregulation of PFN2 mRNA and protein levels, thereby further activating the downstream TGF-β/Smad pathway. Additionally, downregulation of circ0020134 inhibited epithelial-mesenchymal transition (EMT) in CRC cells, which could be reversed by miR-183-5p inhibitor treatment. Collectively, our findings confirm that the circ0020134-miR-183-5p-PFN2-TGF-β/Smad axis induces EMT transformation within tumor cells, promoting CRC proliferation and metastasis, thus highlighting its potential as a therapeutic target for patients with CRC liver metastasis.
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spelling pubmed-106522122023-11-03 Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis Yu, Jin-hao Tan, Jia-nan Zhong, Guang-yu Zhong, Lin Hou, Dong Ma, Shuai Wang, Peng-liang Zhang, Zhi-hong Lu, Xu-qiang Yang, Bin Zhou, Sheng-ning Han, Fang-hai Transl Oncol Original Research Circular RNAs (circRNAs) are a distinct class of non-coding RNAs that play regulatory roles in the initiation and progression of tumors. With advancements in transcriptome sequencing technology, numerous circRNAs that play significant roles in tumor-related genes have been identified. In this study, we used transcriptome sequencing to analyze the expression levels of circRNAs in normal adjacent tissues, primary colorectal cancer (CRC) tissues, and CRC tissues with liver metastasis. We successfully identified the circRNA hsa_circ_0020134 (circ0020134), which exhibited significantly elevated expression specifically in CRC with liver metastasis. Importantly, high levels of circ0020134 were associated with a poor prognosis among patients. Functional experiments demonstrated that circ0020134 promotes the proliferation and metastasis of CRC cells both in vitro and in vivo. Mechanistically, upregulation of circ0020134 was induced by the transcription factor, PAX5, while miR-183-5p acted as a sponge for circ0020134, leading to partial upregulation of PFN2 mRNA and protein levels, thereby further activating the downstream TGF-β/Smad pathway. Additionally, downregulation of circ0020134 inhibited epithelial-mesenchymal transition (EMT) in CRC cells, which could be reversed by miR-183-5p inhibitor treatment. Collectively, our findings confirm that the circ0020134-miR-183-5p-PFN2-TGF-β/Smad axis induces EMT transformation within tumor cells, promoting CRC proliferation and metastasis, thus highlighting its potential as a therapeutic target for patients with CRC liver metastasis. Neoplasia Press 2023-11-03 /pmc/articles/PMC10652212/ /pubmed/37925795 http://dx.doi.org/10.1016/j.tranon.2023.101823 Text en © 2023 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Yu, Jin-hao
Tan, Jia-nan
Zhong, Guang-yu
Zhong, Lin
Hou, Dong
Ma, Shuai
Wang, Peng-liang
Zhang, Zhi-hong
Lu, Xu-qiang
Yang, Bin
Zhou, Sheng-ning
Han, Fang-hai
Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title_full Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title_fullStr Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title_full_unstemmed Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title_short Hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the miR-183-5p-PFN2-TGF-β/Smad axis
title_sort hsa_circ_0020134 promotes liver metastasis of colorectal cancer through the mir-183-5p-pfn2-tgf-β/smad axis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652212/
https://www.ncbi.nlm.nih.gov/pubmed/37925795
http://dx.doi.org/10.1016/j.tranon.2023.101823
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