Cargando…
Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway
Paclitaxel, a known TLR4 ligand, leads to activation of TLR4/MyD88-dependent pathway that mediates chemoresistance and tumor progression in epithelial ovarian carcinoma (EOC). Atractylenolide-I (AO-I), a novel TLR4-antagonizing agent, inhibits TLR4 signaling by interfering with the binding of LPS or...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899591/ https://www.ncbi.nlm.nih.gov/pubmed/24452475 http://dx.doi.org/10.1038/srep03840 |
_version_ | 1782300597561589760 |
---|---|
author | Huang, Jian-Ming Zhang, Guo-Nan Shi, Yu Zha, Xiao Zhu, Yi Wang, Miao-Miao Lin, Qing Wang, Wen Lu, Hai-Yan Ma, Shi-Qi Cheng, Jia Deng, Bi-Fang |
author_facet | Huang, Jian-Ming Zhang, Guo-Nan Shi, Yu Zha, Xiao Zhu, Yi Wang, Miao-Miao Lin, Qing Wang, Wen Lu, Hai-Yan Ma, Shi-Qi Cheng, Jia Deng, Bi-Fang |
author_sort | Huang, Jian-Ming |
collection | PubMed |
description | Paclitaxel, a known TLR4 ligand, leads to activation of TLR4/MyD88-dependent pathway that mediates chemoresistance and tumor progression in epithelial ovarian carcinoma (EOC). Atractylenolide-I (AO-I), a novel TLR4-antagonizing agent, inhibits TLR4 signaling by interfering with the binding of LPS or paclitaxel to membrane TLR4 of human leukocytes. In this study, AO-I was found to attenuate paclitaxel-induced protein expression of IL-6, VEGF and survivin, and to enhance early apoptosis and growth inhibition in MyD88(+) EOC cells; AO-I was shown to fit into the hydrophobic pocket of human MD-2 and to partially overlap with the binding site of paclitaxel by docking simulations, suggesting that AO-I may block the MD-2-mediated TLR4/MyD88-dependent paclitaxel signaling in MyD88(+) EOC cells. Therefore, AO-I could significantly sensitize the response of MyD88(+) EOC cells to paclitaxel by blocking MD-2-mediated TLR4/MyD88 signaling, and that AO-I-paclitaxel combination could be a promising strategy for the treatment of EOC with a functional TLR4/MyD88/NF-κB pathway. |
format | Online Article Text |
id | pubmed-3899591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38995912014-01-24 Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway Huang, Jian-Ming Zhang, Guo-Nan Shi, Yu Zha, Xiao Zhu, Yi Wang, Miao-Miao Lin, Qing Wang, Wen Lu, Hai-Yan Ma, Shi-Qi Cheng, Jia Deng, Bi-Fang Sci Rep Article Paclitaxel, a known TLR4 ligand, leads to activation of TLR4/MyD88-dependent pathway that mediates chemoresistance and tumor progression in epithelial ovarian carcinoma (EOC). Atractylenolide-I (AO-I), a novel TLR4-antagonizing agent, inhibits TLR4 signaling by interfering with the binding of LPS or paclitaxel to membrane TLR4 of human leukocytes. In this study, AO-I was found to attenuate paclitaxel-induced protein expression of IL-6, VEGF and survivin, and to enhance early apoptosis and growth inhibition in MyD88(+) EOC cells; AO-I was shown to fit into the hydrophobic pocket of human MD-2 and to partially overlap with the binding site of paclitaxel by docking simulations, suggesting that AO-I may block the MD-2-mediated TLR4/MyD88-dependent paclitaxel signaling in MyD88(+) EOC cells. Therefore, AO-I could significantly sensitize the response of MyD88(+) EOC cells to paclitaxel by blocking MD-2-mediated TLR4/MyD88 signaling, and that AO-I-paclitaxel combination could be a promising strategy for the treatment of EOC with a functional TLR4/MyD88/NF-κB pathway. Nature Publishing Group 2014-01-23 /pmc/articles/PMC3899591/ /pubmed/24452475 http://dx.doi.org/10.1038/srep03840 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Huang, Jian-Ming Zhang, Guo-Nan Shi, Yu Zha, Xiao Zhu, Yi Wang, Miao-Miao Lin, Qing Wang, Wen Lu, Hai-Yan Ma, Shi-Qi Cheng, Jia Deng, Bi-Fang Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title | Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title_full | Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title_fullStr | Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title_full_unstemmed | Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title_short | Atractylenolide-I Sensitizes Human Ovarian Cancer Cells to Paclitaxel by Blocking Activation of TLR4/MyD88-dependent Pathway |
title_sort | atractylenolide-i sensitizes human ovarian cancer cells to paclitaxel by blocking activation of tlr4/myd88-dependent pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899591/ https://www.ncbi.nlm.nih.gov/pubmed/24452475 http://dx.doi.org/10.1038/srep03840 |
work_keys_str_mv | AT huangjianming atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT zhangguonan atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT shiyu atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT zhaxiao atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT zhuyi atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT wangmiaomiao atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT linqing atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT wangwen atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT luhaiyan atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT mashiqi atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT chengjia atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway AT dengbifang atractylenolideisensitizeshumanovariancancercellstopaclitaxelbyblockingactivationoftlr4myd88dependentpathway |