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Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway
The incidence of cervical cancer is increasing annually worldwide. Low-dose naltrexone (LDN) has been reported to delay tumor progression, but the mechanism remains unclear. Here, we found that low-dose naltrexone could upregulate the expression of OGFr. Additionally, LDN could suppress the abilitie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859308/ https://www.ncbi.nlm.nih.gov/pubmed/33540155 http://dx.doi.org/10.1016/j.tranon.2021.101028 |
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author | Liu, Ning Yan, Limei Shan, Fengping Wang, Xiaonai Qu, Na Handley, Mike K Ma, Mingxing |
author_facet | Liu, Ning Yan, Limei Shan, Fengping Wang, Xiaonai Qu, Na Handley, Mike K Ma, Mingxing |
author_sort | Liu, Ning |
collection | PubMed |
description | The incidence of cervical cancer is increasing annually worldwide. Low-dose naltrexone (LDN) has been reported to delay tumor progression, but the mechanism remains unclear. Here, we found that low-dose naltrexone could upregulate the expression of OGFr. Additionally, LDN could suppress the abilities of colony formation, migration and invasion in cervical cancer cells. LDN could also inhibit cervical cancer progression in mice model. Moreover, LDN indirectly reduced the expressions of PI3K, pAKT and mTOR in vitro and in vivo. Therefore, LDN may be considered a potential treatment option for cervical cancer. |
format | Online Article Text |
id | pubmed-7859308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78593082021-02-09 Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway Liu, Ning Yan, Limei Shan, Fengping Wang, Xiaonai Qu, Na Handley, Mike K Ma, Mingxing Transl Oncol Original Research The incidence of cervical cancer is increasing annually worldwide. Low-dose naltrexone (LDN) has been reported to delay tumor progression, but the mechanism remains unclear. Here, we found that low-dose naltrexone could upregulate the expression of OGFr. Additionally, LDN could suppress the abilities of colony formation, migration and invasion in cervical cancer cells. LDN could also inhibit cervical cancer progression in mice model. Moreover, LDN indirectly reduced the expressions of PI3K, pAKT and mTOR in vitro and in vivo. Therefore, LDN may be considered a potential treatment option for cervical cancer. Neoplasia Press 2021-02-01 /pmc/articles/PMC7859308/ /pubmed/33540155 http://dx.doi.org/10.1016/j.tranon.2021.101028 Text en © 2021 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Research Liu, Ning Yan, Limei Shan, Fengping Wang, Xiaonai Qu, Na Handley, Mike K Ma, Mingxing Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title | Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title_full | Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title_fullStr | Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title_full_unstemmed | Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title_short | Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway |
title_sort | low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing pi3k/akt/mtor pathway |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859308/ https://www.ncbi.nlm.nih.gov/pubmed/33540155 http://dx.doi.org/10.1016/j.tranon.2021.101028 |
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