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RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment

Shikonin is a naphthoquinone isolated from the dried root of Lithospermum erythrorhizon, an herb used in Chinese medicine. Although several studies have indicated that shikonin exhibits antitumor activity in breast cancer, the mechanism of action remains unclear. In the present study, we performed t...

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Autores principales: Lin, Kuo-Hua, Huang, Ming-Yii, Cheng, Wei-Chung, Wang, Shu-Chi, Fang, Shih-Hua, Tu, Hung-Pin, Su, Chia-Cheng, Hung, Yung-Li, Liu, Po-Len, Chen, Chi-Shuo, Wang, Yu-Ting, Li, Chia-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805692/
https://www.ncbi.nlm.nih.gov/pubmed/29422643
http://dx.doi.org/10.1038/s41598-018-21065-x
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author Lin, Kuo-Hua
Huang, Ming-Yii
Cheng, Wei-Chung
Wang, Shu-Chi
Fang, Shih-Hua
Tu, Hung-Pin
Su, Chia-Cheng
Hung, Yung-Li
Liu, Po-Len
Chen, Chi-Shuo
Wang, Yu-Ting
Li, Chia-Yang
author_facet Lin, Kuo-Hua
Huang, Ming-Yii
Cheng, Wei-Chung
Wang, Shu-Chi
Fang, Shih-Hua
Tu, Hung-Pin
Su, Chia-Cheng
Hung, Yung-Li
Liu, Po-Len
Chen, Chi-Shuo
Wang, Yu-Ting
Li, Chia-Yang
author_sort Lin, Kuo-Hua
collection PubMed
description Shikonin is a naphthoquinone isolated from the dried root of Lithospermum erythrorhizon, an herb used in Chinese medicine. Although several studies have indicated that shikonin exhibits antitumor activity in breast cancer, the mechanism of action remains unclear. In the present study, we performed transcriptome analysis using RNA-seq and explored the mechanism of action of shikonin in regulating the growth of different types of breast cancer cells. The IC(50) of shikonin on MCF-7, SKBR-3 and MDA-MB-231 cells were 10.3 μΜ, 15.0 μΜ, 15.0 μΜ respectively. Our results also demonstrated that shikonin arrests the progression of cell cycle and induces apoptosis in MDA-MB-231 cells. Using RNA-seq transcriptome analysis, we found 38 common genes that significantly express in different types of breast cancer cells under shikonin treatment. In particular, our results indicated that shikonin induces the expression of dual specificity phosphatase (DUSP)-1 and DUSP2 in both RNA and protein levels. In addition, shikonin also inhibits the phosphorylation of JNK and p38, the downstream signaling molecules of DUSP1 and DUSP2. Therefore, our results suggest that shikonin induces the expression of DUSP1 and DUSP2 which consequently switches off JNK and p38 MAPK pathways and causes cell cycle arrest and apoptosis in breast cancer cells.
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spelling pubmed-58056922018-02-16 RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment Lin, Kuo-Hua Huang, Ming-Yii Cheng, Wei-Chung Wang, Shu-Chi Fang, Shih-Hua Tu, Hung-Pin Su, Chia-Cheng Hung, Yung-Li Liu, Po-Len Chen, Chi-Shuo Wang, Yu-Ting Li, Chia-Yang Sci Rep Article Shikonin is a naphthoquinone isolated from the dried root of Lithospermum erythrorhizon, an herb used in Chinese medicine. Although several studies have indicated that shikonin exhibits antitumor activity in breast cancer, the mechanism of action remains unclear. In the present study, we performed transcriptome analysis using RNA-seq and explored the mechanism of action of shikonin in regulating the growth of different types of breast cancer cells. The IC(50) of shikonin on MCF-7, SKBR-3 and MDA-MB-231 cells were 10.3 μΜ, 15.0 μΜ, 15.0 μΜ respectively. Our results also demonstrated that shikonin arrests the progression of cell cycle and induces apoptosis in MDA-MB-231 cells. Using RNA-seq transcriptome analysis, we found 38 common genes that significantly express in different types of breast cancer cells under shikonin treatment. In particular, our results indicated that shikonin induces the expression of dual specificity phosphatase (DUSP)-1 and DUSP2 in both RNA and protein levels. In addition, shikonin also inhibits the phosphorylation of JNK and p38, the downstream signaling molecules of DUSP1 and DUSP2. Therefore, our results suggest that shikonin induces the expression of DUSP1 and DUSP2 which consequently switches off JNK and p38 MAPK pathways and causes cell cycle arrest and apoptosis in breast cancer cells. Nature Publishing Group UK 2018-02-08 /pmc/articles/PMC5805692/ /pubmed/29422643 http://dx.doi.org/10.1038/s41598-018-21065-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
Lin, Kuo-Hua
Huang, Ming-Yii
Cheng, Wei-Chung
Wang, Shu-Chi
Fang, Shih-Hua
Tu, Hung-Pin
Su, Chia-Cheng
Hung, Yung-Li
Liu, Po-Len
Chen, Chi-Shuo
Wang, Yu-Ting
Li, Chia-Yang
RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title_full RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title_fullStr RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title_full_unstemmed RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title_short RNA-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
title_sort rna-seq transcriptome analysis of breast cancer cell lines under shikonin treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805692/
https://www.ncbi.nlm.nih.gov/pubmed/29422643
http://dx.doi.org/10.1038/s41598-018-21065-x
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