Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.

To study the in vivo and in vitro effects of adding oxygen carbon nanotubes (CNTs) to chemotherapy for breast cancer.MCF-7 and SK-BR-3 breast cancer cells were co-cultured with paclitaxel and then exposed to oxygen-CNTs under hypoxic conditions. Cell proliferation, viability, and apoptosis rate were...

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Main Authors: Yongkun Wang, Chuanying Wang, Yijun Jia, Xianhua Cheng, Qing Lin, Mingjie Zhu, Yunshu Lu, Longlong Ding, Ziyi Weng, Kejin Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4121325?pdf=render
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spelling doaj-293ea5c127dd415eb77206396f5aada52020-11-25T02:37:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0198e10420910.1371/journal.pone.0104209Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.Yongkun WangChuanying WangYijun JiaXianhua ChengQing LinMingjie ZhuYunshu LuLonglong DingZiyi WengKejin WuTo study the in vivo and in vitro effects of adding oxygen carbon nanotubes (CNTs) to chemotherapy for breast cancer.MCF-7 and SK-BR-3 breast cancer cells were co-cultured with paclitaxel and then exposed to oxygen-CNTs under hypoxic conditions. Cell proliferation, viability, and apoptosis rate were analyzed. Hypoxia-inducible factor-1 alpha (HIF-1α) expression was measured using reverse transcription-polymerase chain reaction (RT-PCR) and western blot. Nude mice were used as a human breast cancer model to explore the impact of oxygen-CNTs on the in vivo chemotherapeutic effect of paclitaxel.Oxygen-CNTs had no significant effects on the growth of breast cancer cells under normoxia and hypoxia. However, in the hypoxic environment, oxygen-CNTs significantly enhanced the inhibitory effect of paclitaxel on cell proliferation, as well as the apoptosis rate. Under hypoxia, downregulation of HIF-1α and upregulation of caspase-3, caspase-8, caspase-9, LC3 and Beclin-1 were observed when paclitaxel was combined with oxygen-CNT. Furthermore, addition of oxygen-CNTs to chemotherapy was found to significantly reduce tumor weight in the tumor-bearing mice model.Oxygen-CNTs can significantly increase the chemotherapeutic effect of paclitaxel on breast cancer cells. Oxygen-CNTs may be a potential chemosensitizer in breast cancer therapy.http://europepmc.org/articles/PMC4121325?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yongkun Wang
Chuanying Wang
Yijun Jia
Xianhua Cheng
Qing Lin
Mingjie Zhu
Yunshu Lu
Longlong Ding
Ziyi Weng
Kejin Wu
spellingShingle Yongkun Wang
Chuanying Wang
Yijun Jia
Xianhua Cheng
Qing Lin
Mingjie Zhu
Yunshu Lu
Longlong Ding
Ziyi Weng
Kejin Wu
Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
PLoS ONE
author_facet Yongkun Wang
Chuanying Wang
Yijun Jia
Xianhua Cheng
Qing Lin
Mingjie Zhu
Yunshu Lu
Longlong Ding
Ziyi Weng
Kejin Wu
author_sort Yongkun Wang
title Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
title_short Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
title_full Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
title_fullStr Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
title_full_unstemmed Oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
title_sort oxygen-carbon nanotubes as a chemotherapy sensitizer for paclitaxel in breast cancer treatment.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description To study the in vivo and in vitro effects of adding oxygen carbon nanotubes (CNTs) to chemotherapy for breast cancer.MCF-7 and SK-BR-3 breast cancer cells were co-cultured with paclitaxel and then exposed to oxygen-CNTs under hypoxic conditions. Cell proliferation, viability, and apoptosis rate were analyzed. Hypoxia-inducible factor-1 alpha (HIF-1α) expression was measured using reverse transcription-polymerase chain reaction (RT-PCR) and western blot. Nude mice were used as a human breast cancer model to explore the impact of oxygen-CNTs on the in vivo chemotherapeutic effect of paclitaxel.Oxygen-CNTs had no significant effects on the growth of breast cancer cells under normoxia and hypoxia. However, in the hypoxic environment, oxygen-CNTs significantly enhanced the inhibitory effect of paclitaxel on cell proliferation, as well as the apoptosis rate. Under hypoxia, downregulation of HIF-1α and upregulation of caspase-3, caspase-8, caspase-9, LC3 and Beclin-1 were observed when paclitaxel was combined with oxygen-CNT. Furthermore, addition of oxygen-CNTs to chemotherapy was found to significantly reduce tumor weight in the tumor-bearing mice model.Oxygen-CNTs can significantly increase the chemotherapeutic effect of paclitaxel on breast cancer cells. Oxygen-CNTs may be a potential chemosensitizer in breast cancer therapy.
url http://europepmc.org/articles/PMC4121325?pdf=render
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