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A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198

INTRODUCTION: Circular RNAs (circRNAs), a new type of non-coding RNA, have been demonstrated to play critical roles in the progression of various of malignant cancers. However, the function of circRNAs in breast cancer is not clearly understood. METHODS: qPCR was used to evaluate the gene expression...

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Autores principales: Zhang, Zhaohui, Hu, Hao, Li, Qian, Yi, Fumei, Liu, Yan’e
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590943/
https://www.ncbi.nlm.nih.gov/pubmed/34785951
http://dx.doi.org/10.2147/CMAR.S256091
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author Zhang, Zhaohui
Hu, Hao
Li, Qian
Yi, Fumei
Liu, Yan’e
author_facet Zhang, Zhaohui
Hu, Hao
Li, Qian
Yi, Fumei
Liu, Yan’e
author_sort Zhang, Zhaohui
collection PubMed
description INTRODUCTION: Circular RNAs (circRNAs), a new type of non-coding RNA, have been demonstrated to play critical roles in the progression of various of malignant cancers. However, the function of circRNAs in breast cancer is not clearly understood. METHODS: qPCR was used to evaluate the gene expression. Function studies including MTT, transwell, wound healing and colony formation assay were performed to evaluate the function of circPTCD3 in breast cancer. Luciferase and RNA pull-down assays were used to verify the interaction between circPTCD3 and miR-198. The xenograft model was established to evaluate the function of circPTCD3 in vivo. RESULTS: In the present study, we identified a novel circRNA termed as circPTCD3 which was indicated to be significantly up-regulated in breast cancer tissues and cell lines. The results revealed that ectopic expression of circPTCD3 promoted the cell proliferation, migration and colony formation ability of breast cancer cells. Constantly, silencing of circPTCD3 inhibited those of breast cancer cells. Furthermore, we identified that circPTCD3 was able to target miR-198 in breast cancer cell. miR-198 has the function of inhibiting proliferation and migration of breast cancer cells which can be reversed by circPTCD3. CONCLUSION: Taken together, our findings for the first time identified a novel circRNA (circPTCD3) and revealed its oncogenic role in breast cancer. Mechanically, we reported that circPTCD3 served as a competing endogenous RNA (ceRNA) to sponge miR-198. These findings provide insights into breast cancer progression and also potential new targets for diagnosis or treatment of breast cancer.
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spelling pubmed-85909432021-11-15 A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198 Zhang, Zhaohui Hu, Hao Li, Qian Yi, Fumei Liu, Yan’e Cancer Manag Res Original Research INTRODUCTION: Circular RNAs (circRNAs), a new type of non-coding RNA, have been demonstrated to play critical roles in the progression of various of malignant cancers. However, the function of circRNAs in breast cancer is not clearly understood. METHODS: qPCR was used to evaluate the gene expression. Function studies including MTT, transwell, wound healing and colony formation assay were performed to evaluate the function of circPTCD3 in breast cancer. Luciferase and RNA pull-down assays were used to verify the interaction between circPTCD3 and miR-198. The xenograft model was established to evaluate the function of circPTCD3 in vivo. RESULTS: In the present study, we identified a novel circRNA termed as circPTCD3 which was indicated to be significantly up-regulated in breast cancer tissues and cell lines. The results revealed that ectopic expression of circPTCD3 promoted the cell proliferation, migration and colony formation ability of breast cancer cells. Constantly, silencing of circPTCD3 inhibited those of breast cancer cells. Furthermore, we identified that circPTCD3 was able to target miR-198 in breast cancer cell. miR-198 has the function of inhibiting proliferation and migration of breast cancer cells which can be reversed by circPTCD3. CONCLUSION: Taken together, our findings for the first time identified a novel circRNA (circPTCD3) and revealed its oncogenic role in breast cancer. Mechanically, we reported that circPTCD3 served as a competing endogenous RNA (ceRNA) to sponge miR-198. These findings provide insights into breast cancer progression and also potential new targets for diagnosis or treatment of breast cancer. Dove 2021-11-10 /pmc/articles/PMC8590943/ /pubmed/34785951 http://dx.doi.org/10.2147/CMAR.S256091 Text en © 2021 Zhang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhang, Zhaohui
Hu, Hao
Li, Qian
Yi, Fumei
Liu, Yan’e
A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title_full A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title_fullStr A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title_full_unstemmed A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title_short A Novel Circular RNA circPTCD3 Promotes Breast Cancer Progression Through Sponging miR-198
title_sort novel circular rna circptcd3 promotes breast cancer progression through sponging mir-198
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590943/
https://www.ncbi.nlm.nih.gov/pubmed/34785951
http://dx.doi.org/10.2147/CMAR.S256091
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