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Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel

Cancer growth is usually accompanied by metastasis which kills most cancer patients. Here we aim to study the effect of cisplatin at different doses on breast cancer growth and metastasis. Methods: We used cisplatin to treat breast cancer cells, then detected the migration of cells and the changes o...

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Autores principales: Wang, Haitao, Guo, Sen, Kim, Seung-Jin, Shao, Fangyuan, Ho, Joshua Wing Kei, Wong, Kuan Un, Miao, Zhengqiang, Hao, Dapeng, Zhao, Ming, Xu, Jun, Zeng, Jianming, Wong, Koon Ho, Di, Lijun, Wong, Ada Hang-Heng, Xu, Xiaoling, Deng, Chu-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797698/
https://www.ncbi.nlm.nih.gov/pubmed/33500735
http://dx.doi.org/10.7150/thno.46460
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author Wang, Haitao
Guo, Sen
Kim, Seung-Jin
Shao, Fangyuan
Ho, Joshua Wing Kei
Wong, Kuan Un
Miao, Zhengqiang
Hao, Dapeng
Zhao, Ming
Xu, Jun
Zeng, Jianming
Wong, Koon Ho
Di, Lijun
Wong, Ada Hang-Heng
Xu, Xiaoling
Deng, Chu-Xia
author_facet Wang, Haitao
Guo, Sen
Kim, Seung-Jin
Shao, Fangyuan
Ho, Joshua Wing Kei
Wong, Kuan Un
Miao, Zhengqiang
Hao, Dapeng
Zhao, Ming
Xu, Jun
Zeng, Jianming
Wong, Koon Ho
Di, Lijun
Wong, Ada Hang-Heng
Xu, Xiaoling
Deng, Chu-Xia
author_sort Wang, Haitao
collection PubMed
description Cancer growth is usually accompanied by metastasis which kills most cancer patients. Here we aim to study the effect of cisplatin at different doses on breast cancer growth and metastasis. Methods: We used cisplatin to treat breast cancer cells, then detected the migration of cells and the changes of epithelial-mesenchymal transition (EMT) markers by migration assay, Western blot, and immunofluorescent staining. Next, we analyzed the changes of RNA expression of genes by RNA-seq and confirmed the binding of activating transcription factor 3 (ATF3) to cytoskeleton related genes by ChIP-seq. Thereafter, we combined cisplatin and paclitaxel in a neoadjuvant setting to treat xenograft mouse models. Furthermore, we analyzed the association of disease prognosis with cytoskeletal genes and ATF3 by clinical data analysis. Results: When administered at a higher dose (6 mg/kg), cisplatin inhibits both cancer growth and metastasis, yet with strong side effects, whereas a lower dose (2 mg/kg) cisplatin blocks cancer metastasis without obvious killing effects. Cisplatin inhibits cancer metastasis through blocking early steps of EMT. It antagonizes transforming growth factor beta (TGFβ) signaling through suppressing transcription of many genes involved in cytoskeleton reorganization and filopodia formation which occur early in EMT and are responsible for cancer metastasis. Mechanistically, TGFβ and fibronectin-1 (FN1) constitute a positive reciprocal regulation loop that is critical for activating TGFβ/SMAD3 signaling, which is repressed by cisplatin induced expression of ATF3. Furthermore, neoadjuvant administration of cisplatin at 2 mg/kg in conjunction with paclitaxel inhibits cancer growth and blocks metastasis without causing obvious side effects by inhibiting colonization of cancer cells in the target organs. Conclusion: Thus, cisplatin prevents breast cancer metastasis through blocking early EMT, and the combination of cisplatin and paclitaxel represents a promising therapy for killing breast cancer and blocking tumor metastasis.
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spelling pubmed-77976982021-01-25 Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel Wang, Haitao Guo, Sen Kim, Seung-Jin Shao, Fangyuan Ho, Joshua Wing Kei Wong, Kuan Un Miao, Zhengqiang Hao, Dapeng Zhao, Ming Xu, Jun Zeng, Jianming Wong, Koon Ho Di, Lijun Wong, Ada Hang-Heng Xu, Xiaoling Deng, Chu-Xia Theranostics Research Paper Cancer growth is usually accompanied by metastasis which kills most cancer patients. Here we aim to study the effect of cisplatin at different doses on breast cancer growth and metastasis. Methods: We used cisplatin to treat breast cancer cells, then detected the migration of cells and the changes of epithelial-mesenchymal transition (EMT) markers by migration assay, Western blot, and immunofluorescent staining. Next, we analyzed the changes of RNA expression of genes by RNA-seq and confirmed the binding of activating transcription factor 3 (ATF3) to cytoskeleton related genes by ChIP-seq. Thereafter, we combined cisplatin and paclitaxel in a neoadjuvant setting to treat xenograft mouse models. Furthermore, we analyzed the association of disease prognosis with cytoskeletal genes and ATF3 by clinical data analysis. Results: When administered at a higher dose (6 mg/kg), cisplatin inhibits both cancer growth and metastasis, yet with strong side effects, whereas a lower dose (2 mg/kg) cisplatin blocks cancer metastasis without obvious killing effects. Cisplatin inhibits cancer metastasis through blocking early steps of EMT. It antagonizes transforming growth factor beta (TGFβ) signaling through suppressing transcription of many genes involved in cytoskeleton reorganization and filopodia formation which occur early in EMT and are responsible for cancer metastasis. Mechanistically, TGFβ and fibronectin-1 (FN1) constitute a positive reciprocal regulation loop that is critical for activating TGFβ/SMAD3 signaling, which is repressed by cisplatin induced expression of ATF3. Furthermore, neoadjuvant administration of cisplatin at 2 mg/kg in conjunction with paclitaxel inhibits cancer growth and blocks metastasis without causing obvious side effects by inhibiting colonization of cancer cells in the target organs. Conclusion: Thus, cisplatin prevents breast cancer metastasis through blocking early EMT, and the combination of cisplatin and paclitaxel represents a promising therapy for killing breast cancer and blocking tumor metastasis. Ivyspring International Publisher 2021-01-01 /pmc/articles/PMC7797698/ /pubmed/33500735 http://dx.doi.org/10.7150/thno.46460 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Haitao
Guo, Sen
Kim, Seung-Jin
Shao, Fangyuan
Ho, Joshua Wing Kei
Wong, Kuan Un
Miao, Zhengqiang
Hao, Dapeng
Zhao, Ming
Xu, Jun
Zeng, Jianming
Wong, Koon Ho
Di, Lijun
Wong, Ada Hang-Heng
Xu, Xiaoling
Deng, Chu-Xia
Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title_full Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title_fullStr Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title_full_unstemmed Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title_short Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel
title_sort cisplatin prevents breast cancer metastasis through blocking early emt and retards cancer growth together with paclitaxel
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797698/
https://www.ncbi.nlm.nih.gov/pubmed/33500735
http://dx.doi.org/10.7150/thno.46460
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