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LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer
Cervical cancer (CC) is one of the deadliest female malignancies worldwide. Long non-coding RNAs (lncRNAs) are essential regulators for cancer progression. This study aimed to elucidate the role of lncRNA LINC01305 in the progression of CC. We found where LINC01305 was expressed in CC tissues and it...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386557/ https://www.ncbi.nlm.nih.gov/pubmed/33638945 http://dx.doi.org/10.18632/aging.202565 |
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author | Huang, Xianxia Liu, Xuemei Du, Bo Liu, Xueling Xue, Mei Yan, Qingxin Wang, Xiaohong Wang, Qian |
author_facet | Huang, Xianxia Liu, Xuemei Du, Bo Liu, Xueling Xue, Mei Yan, Qingxin Wang, Xiaohong Wang, Qian |
author_sort | Huang, Xianxia |
collection | PubMed |
description | Cervical cancer (CC) is one of the deadliest female malignancies worldwide. Long non-coding RNAs (lncRNAs) are essential regulators for cancer progression. This study aimed to elucidate the role of lncRNA LINC01305 in the progression of CC. We found where LINC01305 was expressed in CC tissues and its correlation with the survival rate of CC patients. Functional experiments were performed to elucidate the effect of LINC01305 on CC. The results showed that LINC01305 was increased in CC tumor tissues and was correlated with a lower survival rate. The overexpression and knockdown of LINC01305 enhanced and inhibited the progression of CC, respectively. Additionally, the upregulation of LINC01305 promoted tumor growth in xenograft mice. Moreover, the effect of LINC01305 on CC was mediated through interacting with the RNA-binding protein, KHSRP. Furthermore, LINC01305 was mainly distributed in exosomes and was transferred to recipient cells to enhance CC progression. Lastly, LINC01305 may participate in the regulation of the stemness of CC. Taken together, the results suggest that LINC01305 promotes the progression of CC through KHSRP and that LINC01305 is released through exosomes and is involved in the stemness of CC. This study sheds light on the molecular mechanism underlying the progression of CC. |
format | Online Article Text |
id | pubmed-8386557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-83865572021-08-27 LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer Huang, Xianxia Liu, Xuemei Du, Bo Liu, Xueling Xue, Mei Yan, Qingxin Wang, Xiaohong Wang, Qian Aging (Albany NY) Research Paper Cervical cancer (CC) is one of the deadliest female malignancies worldwide. Long non-coding RNAs (lncRNAs) are essential regulators for cancer progression. This study aimed to elucidate the role of lncRNA LINC01305 in the progression of CC. We found where LINC01305 was expressed in CC tissues and its correlation with the survival rate of CC patients. Functional experiments were performed to elucidate the effect of LINC01305 on CC. The results showed that LINC01305 was increased in CC tumor tissues and was correlated with a lower survival rate. The overexpression and knockdown of LINC01305 enhanced and inhibited the progression of CC, respectively. Additionally, the upregulation of LINC01305 promoted tumor growth in xenograft mice. Moreover, the effect of LINC01305 on CC was mediated through interacting with the RNA-binding protein, KHSRP. Furthermore, LINC01305 was mainly distributed in exosomes and was transferred to recipient cells to enhance CC progression. Lastly, LINC01305 may participate in the regulation of the stemness of CC. Taken together, the results suggest that LINC01305 promotes the progression of CC through KHSRP and that LINC01305 is released through exosomes and is involved in the stemness of CC. This study sheds light on the molecular mechanism underlying the progression of CC. Impact Journals 2021-02-26 /pmc/articles/PMC8386557/ /pubmed/33638945 http://dx.doi.org/10.18632/aging.202565 Text en Copyright: © 2021 Huang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Huang, Xianxia Liu, Xuemei Du, Bo Liu, Xueling Xue, Mei Yan, Qingxin Wang, Xiaohong Wang, Qian LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title | LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title_full | LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title_fullStr | LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title_full_unstemmed | LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title_short | LncRNA LINC01305 promotes cervical cancer progression through KHSRP and exosome-mediated transfer |
title_sort | lncrna linc01305 promotes cervical cancer progression through khsrp and exosome-mediated transfer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386557/ https://www.ncbi.nlm.nih.gov/pubmed/33638945 http://dx.doi.org/10.18632/aging.202565 |
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