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Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer
This study aimed to investigate whether lidocaine, alone or in combination with other chemotherapeutic agents, inhibits the growth of human bladder cancer cells in vitro and orthotopically transplanted bladder tumors in vivo. The effects of lidocaine (1.25, 2.5 or 5 mg/mL), mitomycin C (MMC, 0.66 mg...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766619/ https://www.ncbi.nlm.nih.gov/pubmed/29330444 http://dx.doi.org/10.1038/s41598-017-19026-x |
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author | Yang, Xihua Zhao, Lili Li, Meiping Yan, Lei Zhang, Shengwan Mi, Zhenguo Ren, Liansheng Xu, Jun |
author_facet | Yang, Xihua Zhao, Lili Li, Meiping Yan, Lei Zhang, Shengwan Mi, Zhenguo Ren, Liansheng Xu, Jun |
author_sort | Yang, Xihua |
collection | PubMed |
description | This study aimed to investigate whether lidocaine, alone or in combination with other chemotherapeutic agents, inhibits the growth of human bladder cancer cells in vitro and orthotopically transplanted bladder tumors in vivo. The effects of lidocaine (1.25, 2.5 or 5 mg/mL), mitomycin C (MMC, 0.66 mg/mL), pirarubicin (0.75 mg/mL) and Su Fu’ning lotion (SFN, 0.0625 mg/mL) on the proliferation of human bladder cancer (BIU-87) cells were studied using the MTT assay. A Balb/c nude mouse model of bladder cancer was developed by orthotopic transplantation of BIU-87 cells, and the effects of intravesical instillation of lidocaine and MMC on bladder wet weight (a measure of tumor size) and survival (over 60 days) were studied. Lidocaine inhibited proliferation of BIU-87 cells in a concentration-dependent manner and (when given in combination) enhanced the actions of each of the other antiproliferative agents. In tumor-bearing mice, MMC alone had no effect on mean survival or bladder wet weight. However, the combination of 0.66 mg/mL MMC and 5 mg/mL lidocaine prolonged survival (from 34.62 ± 6.49 to 49.30 ± 6.72 days; n = 8, P < 0.05) and reduced bladder wet weight (from 68.94 ± 53.61 to 20.26 ± 6.07; n = 8, P < 0.05). Intravesical instillation of lidocaine combined with other chemotherapeutic agents potentially could be an effective therapy for bladder cancer. |
format | Online Article Text |
id | pubmed-5766619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57666192018-01-25 Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer Yang, Xihua Zhao, Lili Li, Meiping Yan, Lei Zhang, Shengwan Mi, Zhenguo Ren, Liansheng Xu, Jun Sci Rep Article This study aimed to investigate whether lidocaine, alone or in combination with other chemotherapeutic agents, inhibits the growth of human bladder cancer cells in vitro and orthotopically transplanted bladder tumors in vivo. The effects of lidocaine (1.25, 2.5 or 5 mg/mL), mitomycin C (MMC, 0.66 mg/mL), pirarubicin (0.75 mg/mL) and Su Fu’ning lotion (SFN, 0.0625 mg/mL) on the proliferation of human bladder cancer (BIU-87) cells were studied using the MTT assay. A Balb/c nude mouse model of bladder cancer was developed by orthotopic transplantation of BIU-87 cells, and the effects of intravesical instillation of lidocaine and MMC on bladder wet weight (a measure of tumor size) and survival (over 60 days) were studied. Lidocaine inhibited proliferation of BIU-87 cells in a concentration-dependent manner and (when given in combination) enhanced the actions of each of the other antiproliferative agents. In tumor-bearing mice, MMC alone had no effect on mean survival or bladder wet weight. However, the combination of 0.66 mg/mL MMC and 5 mg/mL lidocaine prolonged survival (from 34.62 ± 6.49 to 49.30 ± 6.72 days; n = 8, P < 0.05) and reduced bladder wet weight (from 68.94 ± 53.61 to 20.26 ± 6.07; n = 8, P < 0.05). Intravesical instillation of lidocaine combined with other chemotherapeutic agents potentially could be an effective therapy for bladder cancer. Nature Publishing Group UK 2018-01-12 /pmc/articles/PMC5766619/ /pubmed/29330444 http://dx.doi.org/10.1038/s41598-017-19026-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yang, Xihua Zhao, Lili Li, Meiping Yan, Lei Zhang, Shengwan Mi, Zhenguo Ren, Liansheng Xu, Jun Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title | Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title_full | Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title_fullStr | Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title_full_unstemmed | Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title_short | Lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
title_sort | lidocaine enhances the effects of chemotherapeutic drugs against bladder cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766619/ https://www.ncbi.nlm.nih.gov/pubmed/29330444 http://dx.doi.org/10.1038/s41598-017-19026-x |
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