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Aberrant Expression of miR-1301 in Human Cancer

miR-1301 is a newly discovered miRNA, which is abnormally expressed in 14 types of tumors. miR-1301 inhibits 23 target genes, forms a ceRNA network with 2 circRNAs and 8 lncRNAs, and participates in 6 signaling pathways, thereby affecting tumor cell proliferation, invasion, metastasis, apoptosis, an...

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Detalles Bibliográficos
Autores principales: Zhong, Chenming, Dong, Yiyao, Zhang, Qiudan, Yuan, Chunhui, Duan, Shiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767067/
https://www.ncbi.nlm.nih.gov/pubmed/35070996
http://dx.doi.org/10.3389/fonc.2021.789626
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author Zhong, Chenming
Dong, Yiyao
Zhang, Qiudan
Yuan, Chunhui
Duan, Shiwei
author_facet Zhong, Chenming
Dong, Yiyao
Zhang, Qiudan
Yuan, Chunhui
Duan, Shiwei
author_sort Zhong, Chenming
collection PubMed
description miR-1301 is a newly discovered miRNA, which is abnormally expressed in 14 types of tumors. miR-1301 inhibits 23 target genes, forms a ceRNA network with 2 circRNAs and 8 lncRNAs, and participates in 6 signaling pathways, thereby affecting tumor cell proliferation, invasion, metastasis, apoptosis, angiogenesis, etc. Abnormal expression of miR-1301 is often associated with poor prognosis of cancer patients. In addition, miR-1301 is related to the anti-tumor effect of epirubicin on osteosarcoma and imatinib on chronic myeloid leukemia(CML) and can enhance the cisplatin sensitivity of ovarian cancer. This work systematically summarizes the abnormal expression and prognostic value of miR-1301 in a variety of cancers, depicts the miR-1301-related signaling pathways and ceRNA network, and provides potential clues for future miR-1301 research.
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spelling pubmed-87670672022-01-20 Aberrant Expression of miR-1301 in Human Cancer Zhong, Chenming Dong, Yiyao Zhang, Qiudan Yuan, Chunhui Duan, Shiwei Front Oncol Oncology miR-1301 is a newly discovered miRNA, which is abnormally expressed in 14 types of tumors. miR-1301 inhibits 23 target genes, forms a ceRNA network with 2 circRNAs and 8 lncRNAs, and participates in 6 signaling pathways, thereby affecting tumor cell proliferation, invasion, metastasis, apoptosis, angiogenesis, etc. Abnormal expression of miR-1301 is often associated with poor prognosis of cancer patients. In addition, miR-1301 is related to the anti-tumor effect of epirubicin on osteosarcoma and imatinib on chronic myeloid leukemia(CML) and can enhance the cisplatin sensitivity of ovarian cancer. This work systematically summarizes the abnormal expression and prognostic value of miR-1301 in a variety of cancers, depicts the miR-1301-related signaling pathways and ceRNA network, and provides potential clues for future miR-1301 research. Frontiers Media S.A. 2022-01-05 /pmc/articles/PMC8767067/ /pubmed/35070996 http://dx.doi.org/10.3389/fonc.2021.789626 Text en Copyright © 2022 Zhong, Dong, Zhang, Yuan and Duan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zhong, Chenming
Dong, Yiyao
Zhang, Qiudan
Yuan, Chunhui
Duan, Shiwei
Aberrant Expression of miR-1301 in Human Cancer
title Aberrant Expression of miR-1301 in Human Cancer
title_full Aberrant Expression of miR-1301 in Human Cancer
title_fullStr Aberrant Expression of miR-1301 in Human Cancer
title_full_unstemmed Aberrant Expression of miR-1301 in Human Cancer
title_short Aberrant Expression of miR-1301 in Human Cancer
title_sort aberrant expression of mir-1301 in human cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767067/
https://www.ncbi.nlm.nih.gov/pubmed/35070996
http://dx.doi.org/10.3389/fonc.2021.789626
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