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Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells

Cervical cancer is the second most common cause of cancer death in women worldwide. Lysophosphatidic acid (LPA) level has been found significantly increased in the serum of patients with ovarian, cervical, and colon cancers. LPA level in cervical cancer patients is significantly higher than in healt...

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Autores principales: Sui, Yanxia, Yang, Ya, Wang, Ji, Li, Yi, Ma, Hongbing, Cai, Hui, Liu, Xiaoping, Zhang, Yong, Wang, Shufeng, Li, Zongfang, Zhang, Xiaozhi, Wang, Jiansheng, Liu, Rui, Yan, Yanli, Xue, Chaofan, Shi, Xiaowei, Tan, Li, Ren, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558435/
https://www.ncbi.nlm.nih.gov/pubmed/26366416
http://dx.doi.org/10.1155/2015/598386
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author Sui, Yanxia
Yang, Ya
Wang, Ji
Li, Yi
Ma, Hongbing
Cai, Hui
Liu, Xiaoping
Zhang, Yong
Wang, Shufeng
Li, Zongfang
Zhang, Xiaozhi
Wang, Jiansheng
Liu, Rui
Yan, Yanli
Xue, Chaofan
Shi, Xiaowei
Tan, Li
Ren, Juan
author_facet Sui, Yanxia
Yang, Ya
Wang, Ji
Li, Yi
Ma, Hongbing
Cai, Hui
Liu, Xiaoping
Zhang, Yong
Wang, Shufeng
Li, Zongfang
Zhang, Xiaozhi
Wang, Jiansheng
Liu, Rui
Yan, Yanli
Xue, Chaofan
Shi, Xiaowei
Tan, Li
Ren, Juan
author_sort Sui, Yanxia
collection PubMed
description Cervical cancer is the second most common cause of cancer death in women worldwide. Lysophosphatidic acid (LPA) level has been found significantly increased in the serum of patients with ovarian, cervical, and colon cancers. LPA level in cervical cancer patients is significantly higher than in healthy controls. LPA receptors were found highly expressed in cervical cancer cells, suggesting LPA may play a role in the development of cervical cancer. The aim of this study is to investigate the effect of LPA on the apoptosis induced by cisplatin (DDP) in cervical cancer cell line and the underlying changes in signaling pathways. Our study found that cisplatin induced apoptosis of Hela cell through inhibiting expression of Bcl-2, upregulating the expression of Bax, Fas-L, and the enzyme activity of caspase-3 (p < 0.05); LPA significantly provided protection against the apoptosis induced by cisplatin by inhibiting the above alterations in apoptotic factor caused by cisplatin (p < 0.05). Moreover, PI3K/AKT pathway was found to be important for the LPA antiapoptosis effect, and administration of PI3K/AKT partially reversed the LPA-mediated protection against cisplatin-induced apoptosis (p < 0.05). These findings have shed new lights on the LPA bioactivity in cervical cancer cells and pointed to a possible sensitization scheme through combined administration of PI3K inhibitor and cisplatin for better treatment of cervical cancer patients, especially those with elevated LPA levels.
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spelling pubmed-45584352015-09-13 Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells Sui, Yanxia Yang, Ya Wang, Ji Li, Yi Ma, Hongbing Cai, Hui Liu, Xiaoping Zhang, Yong Wang, Shufeng Li, Zongfang Zhang, Xiaozhi Wang, Jiansheng Liu, Rui Yan, Yanli Xue, Chaofan Shi, Xiaowei Tan, Li Ren, Juan Biomed Res Int Research Article Cervical cancer is the second most common cause of cancer death in women worldwide. Lysophosphatidic acid (LPA) level has been found significantly increased in the serum of patients with ovarian, cervical, and colon cancers. LPA level in cervical cancer patients is significantly higher than in healthy controls. LPA receptors were found highly expressed in cervical cancer cells, suggesting LPA may play a role in the development of cervical cancer. The aim of this study is to investigate the effect of LPA on the apoptosis induced by cisplatin (DDP) in cervical cancer cell line and the underlying changes in signaling pathways. Our study found that cisplatin induced apoptosis of Hela cell through inhibiting expression of Bcl-2, upregulating the expression of Bax, Fas-L, and the enzyme activity of caspase-3 (p < 0.05); LPA significantly provided protection against the apoptosis induced by cisplatin by inhibiting the above alterations in apoptotic factor caused by cisplatin (p < 0.05). Moreover, PI3K/AKT pathway was found to be important for the LPA antiapoptosis effect, and administration of PI3K/AKT partially reversed the LPA-mediated protection against cisplatin-induced apoptosis (p < 0.05). These findings have shed new lights on the LPA bioactivity in cervical cancer cells and pointed to a possible sensitization scheme through combined administration of PI3K inhibitor and cisplatin for better treatment of cervical cancer patients, especially those with elevated LPA levels. Hindawi Publishing Corporation 2015 2015-08-20 /pmc/articles/PMC4558435/ /pubmed/26366416 http://dx.doi.org/10.1155/2015/598386 Text en Copyright © 2015 Yanxia Sui et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sui, Yanxia
Yang, Ya
Wang, Ji
Li, Yi
Ma, Hongbing
Cai, Hui
Liu, Xiaoping
Zhang, Yong
Wang, Shufeng
Li, Zongfang
Zhang, Xiaozhi
Wang, Jiansheng
Liu, Rui
Yan, Yanli
Xue, Chaofan
Shi, Xiaowei
Tan, Li
Ren, Juan
Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title_full Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title_fullStr Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title_full_unstemmed Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title_short Lysophosphatidic Acid Inhibits Apoptosis Induced by Cisplatin in Cervical Cancer Cells
title_sort lysophosphatidic acid inhibits apoptosis induced by cisplatin in cervical cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558435/
https://www.ncbi.nlm.nih.gov/pubmed/26366416
http://dx.doi.org/10.1155/2015/598386
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