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Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy
Cervical carcinoma is one of the main causes of women’s cancer, and substantial side effects from standard treatment including platinum-based chemotherapy limit the options for escalation. In this paper, using cervical cancer cell lines and tumor-bearing mice as models, we report that CONPs could in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617408/ https://www.ncbi.nlm.nih.gov/pubmed/28977848 http://dx.doi.org/10.18632/oncotarget.17854 |
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author | Xia, Leilei Wang, Ye Chen, Ya Yan, Jiuqiong Hao, Fan Su, Xiaoling Zhang, Caihong Xu, Mingjuan |
author_facet | Xia, Leilei Wang, Ye Chen, Ya Yan, Jiuqiong Hao, Fan Su, Xiaoling Zhang, Caihong Xu, Mingjuan |
author_sort | Xia, Leilei |
collection | PubMed |
description | Cervical carcinoma is one of the main causes of women’s cancer, and substantial side effects from standard treatment including platinum-based chemotherapy limit the options for escalation. In this paper, using cervical cancer cell lines and tumor-bearing mice as models, we report that CONPs could inhibit the proliferation of cancer cells in vitro and in vivo. Especially CONPs could inhibit tumor growth as cisplatin without weight loss. CONPs could also induce autophagy through AKT/mTOR pathway, which demonstrates that CONPs has the potential clinical applications. |
format | Online Article Text |
id | pubmed-5617408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56174082017-10-03 Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy Xia, Leilei Wang, Ye Chen, Ya Yan, Jiuqiong Hao, Fan Su, Xiaoling Zhang, Caihong Xu, Mingjuan Oncotarget Research Paper Cervical carcinoma is one of the main causes of women’s cancer, and substantial side effects from standard treatment including platinum-based chemotherapy limit the options for escalation. In this paper, using cervical cancer cell lines and tumor-bearing mice as models, we report that CONPs could inhibit the proliferation of cancer cells in vitro and in vivo. Especially CONPs could inhibit tumor growth as cisplatin without weight loss. CONPs could also induce autophagy through AKT/mTOR pathway, which demonstrates that CONPs has the potential clinical applications. Impact Journals LLC 2017-05-15 /pmc/articles/PMC5617408/ /pubmed/28977848 http://dx.doi.org/10.18632/oncotarget.17854 Text en Copyright: © 2017 Xia et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 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 Xia, Leilei Wang, Ye Chen, Ya Yan, Jiuqiong Hao, Fan Su, Xiaoling Zhang, Caihong Xu, Mingjuan Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title | Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title_full | Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title_fullStr | Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title_full_unstemmed | Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title_short | Cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
title_sort | cuprous oxide nanoparticles inhibit the growth of cervical carcinoma by inducing autophagy |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617408/ https://www.ncbi.nlm.nih.gov/pubmed/28977848 http://dx.doi.org/10.18632/oncotarget.17854 |
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