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Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells
BACKGROUND: Paclitaxel (Taxol) is a microtubule-stabilizing drug used to treat several solid tumors, including ovarian, breast, non-small cell lung, and pancreatic cancers. The current treatment of ovarian cancer is chemotherapy using paclitaxel in combination with carboplatin as a frontline agent,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408969/ https://www.ncbi.nlm.nih.gov/pubmed/34470602 http://dx.doi.org/10.1186/s12885-021-08722-7 |
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author | Amaya, Celina Luo, Shihua Baigorri, Julio Baucells, Rogelio Smith, Elizabeth R. Xu, Xiang-Xi |
author_facet | Amaya, Celina Luo, Shihua Baigorri, Julio Baucells, Rogelio Smith, Elizabeth R. Xu, Xiang-Xi |
author_sort | Amaya, Celina |
collection | PubMed |
description | BACKGROUND: Paclitaxel (Taxol) is a microtubule-stabilizing drug used to treat several solid tumors, including ovarian, breast, non-small cell lung, and pancreatic cancers. The current treatment of ovarian cancer is chemotherapy using paclitaxel in combination with carboplatin as a frontline agent, and paclitaxel is also used in salvage treatment as a second line drug with a dose intensive regimen following recurrence. More recently, a dose dense approach for paclitaxel has been used to treat metastatic breast cancer with success. Paclitaxel binds to beta tubulin with high affinity and stabilizes microtubule bundles. As a consequence of targeting microtubules, paclitaxel kills cancer cells through inhibition of mitosis, causing mitotic catastrophes, and by additional, not yet well defined non-mitotic mechanism(s). RESULTS: In exploring methods to modulate activity of paclitaxel in causing cancer cell death, we unexpectedly found that a brief exposure of paclitaxel-treated cells in culture to low intensity ultrasound waves prevented the paclitaxel-induced cytotoxicity and death of the cancer cells. The treatment with ultrasound shock waves was found to transiently disrupt the microtubule cytoskeleton and to eliminate paclitaxel-induced rigid microtubule bundles. When cellular microtubules were labelled with a fluorescent paclitaxel analog, exposure to ultrasound waves led to the disassembly of the labeled microtubules and localization of the signals to perinuclear compartments, which were determined to be lysosomes. CONCLUSIONS: We suggest that ultrasound disrupts the paclitaxel-induced rigid microtubule cytoskeleton, generating paclitaxel bound fragments that undergo degradation. A new microtubule network forms from tubulins that are not bound by paclitaxel. Hence, ultrasound shock waves are able to abolish paclitaxel impact on microtubules. Thus, our results demonstrate that a brief exposure to low intensity ultrasound can reduce and/or eliminate cytotoxicity associated with paclitaxel treatment of cancer cells in cultures. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08722-7. |
format | Online Article Text |
id | pubmed-8408969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84089692021-09-01 Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells Amaya, Celina Luo, Shihua Baigorri, Julio Baucells, Rogelio Smith, Elizabeth R. Xu, Xiang-Xi BMC Cancer Research BACKGROUND: Paclitaxel (Taxol) is a microtubule-stabilizing drug used to treat several solid tumors, including ovarian, breast, non-small cell lung, and pancreatic cancers. The current treatment of ovarian cancer is chemotherapy using paclitaxel in combination with carboplatin as a frontline agent, and paclitaxel is also used in salvage treatment as a second line drug with a dose intensive regimen following recurrence. More recently, a dose dense approach for paclitaxel has been used to treat metastatic breast cancer with success. Paclitaxel binds to beta tubulin with high affinity and stabilizes microtubule bundles. As a consequence of targeting microtubules, paclitaxel kills cancer cells through inhibition of mitosis, causing mitotic catastrophes, and by additional, not yet well defined non-mitotic mechanism(s). RESULTS: In exploring methods to modulate activity of paclitaxel in causing cancer cell death, we unexpectedly found that a brief exposure of paclitaxel-treated cells in culture to low intensity ultrasound waves prevented the paclitaxel-induced cytotoxicity and death of the cancer cells. The treatment with ultrasound shock waves was found to transiently disrupt the microtubule cytoskeleton and to eliminate paclitaxel-induced rigid microtubule bundles. When cellular microtubules were labelled with a fluorescent paclitaxel analog, exposure to ultrasound waves led to the disassembly of the labeled microtubules and localization of the signals to perinuclear compartments, which were determined to be lysosomes. CONCLUSIONS: We suggest that ultrasound disrupts the paclitaxel-induced rigid microtubule cytoskeleton, generating paclitaxel bound fragments that undergo degradation. A new microtubule network forms from tubulins that are not bound by paclitaxel. Hence, ultrasound shock waves are able to abolish paclitaxel impact on microtubules. Thus, our results demonstrate that a brief exposure to low intensity ultrasound can reduce and/or eliminate cytotoxicity associated with paclitaxel treatment of cancer cells in cultures. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08722-7. BioMed Central 2021-09-01 /pmc/articles/PMC8408969/ /pubmed/34470602 http://dx.doi.org/10.1186/s12885-021-08722-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Amaya, Celina Luo, Shihua Baigorri, Julio Baucells, Rogelio Smith, Elizabeth R. Xu, Xiang-Xi Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title | Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title_full | Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title_fullStr | Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title_full_unstemmed | Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title_short | Exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
title_sort | exposure to low intensity ultrasound removes paclitaxel cytotoxicity in breast and ovarian cancer cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408969/ https://www.ncbi.nlm.nih.gov/pubmed/34470602 http://dx.doi.org/10.1186/s12885-021-08722-7 |
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