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Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug

Triple negative breast cancer (TNBC) has the poorest prognosis of all types of breast cancer and currently lacks efficient targeted therapy. Chemotherapy is the traditional standard-of-care for TNBC, but is frequently accompanied by severe side effects. Despite the fact that high expression of stero...

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Autores principales: Song, Xianzhou, Zhang, Chengwei, Zhao, Mingkun, Chen, Hui, Liu, Xing, Chen, Jianwei, Lonard, David M., Qin, Li, Xu, Jianming, Wang, Xiaosong, Li, Feng, O’Malley, Bert W., Wang, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592245/
https://www.ncbi.nlm.nih.gov/pubmed/26431029
http://dx.doi.org/10.1371/journal.pone.0140011
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author Song, Xianzhou
Zhang, Chengwei
Zhao, Mingkun
Chen, Hui
Liu, Xing
Chen, Jianwei
Lonard, David M.
Qin, Li
Xu, Jianming
Wang, Xiaosong
Li, Feng
O’Malley, Bert W.
Wang, Jin
author_facet Song, Xianzhou
Zhang, Chengwei
Zhao, Mingkun
Chen, Hui
Liu, Xing
Chen, Jianwei
Lonard, David M.
Qin, Li
Xu, Jianming
Wang, Xiaosong
Li, Feng
O’Malley, Bert W.
Wang, Jin
author_sort Song, Xianzhou
collection PubMed
description Triple negative breast cancer (TNBC) has the poorest prognosis of all types of breast cancer and currently lacks efficient targeted therapy. Chemotherapy is the traditional standard-of-care for TNBC, but is frequently accompanied by severe side effects. Despite the fact that high expression of steroid receptor coactivator 3 (SRC–3) is correlated with poor survival in estrogen receptor positive breast cancer patients, its role in TNBC has not been extensively investigated. Here, we show that high expression of SRC–3 correlates with both poor overall survival and post progression survival in TNBC patients, suggesting that SRC–3 can serve as a prognostic marker for TNBC. Furthermore, we demonstrated that bufalin, a SRC–3 small molecule inhibitor, when introduced even at nM concentrations, can significantly reduce TNBC cell viability and motility. However, because bufalin has minimal water solubility, its in vivo application is limited. Therefore, we developed a water soluble prodrug, 3-phospho-bufalin, to facilitate its in vivo administration. In addition, we demonstrated that 3-phospho-bufalin can effectively inhibit tumor growth in an orthotopic TNBC mouse model, suggesting its potential application as a targeted therapy for TNBC treatment.
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spelling pubmed-45922452015-10-09 Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug Song, Xianzhou Zhang, Chengwei Zhao, Mingkun Chen, Hui Liu, Xing Chen, Jianwei Lonard, David M. Qin, Li Xu, Jianming Wang, Xiaosong Li, Feng O’Malley, Bert W. Wang, Jin PLoS One Research Article Triple negative breast cancer (TNBC) has the poorest prognosis of all types of breast cancer and currently lacks efficient targeted therapy. Chemotherapy is the traditional standard-of-care for TNBC, but is frequently accompanied by severe side effects. Despite the fact that high expression of steroid receptor coactivator 3 (SRC–3) is correlated with poor survival in estrogen receptor positive breast cancer patients, its role in TNBC has not been extensively investigated. Here, we show that high expression of SRC–3 correlates with both poor overall survival and post progression survival in TNBC patients, suggesting that SRC–3 can serve as a prognostic marker for TNBC. Furthermore, we demonstrated that bufalin, a SRC–3 small molecule inhibitor, when introduced even at nM concentrations, can significantly reduce TNBC cell viability and motility. However, because bufalin has minimal water solubility, its in vivo application is limited. Therefore, we developed a water soluble prodrug, 3-phospho-bufalin, to facilitate its in vivo administration. In addition, we demonstrated that 3-phospho-bufalin can effectively inhibit tumor growth in an orthotopic TNBC mouse model, suggesting its potential application as a targeted therapy for TNBC treatment. Public Library of Science 2015-10-02 /pmc/articles/PMC4592245/ /pubmed/26431029 http://dx.doi.org/10.1371/journal.pone.0140011 Text en © 2015 Song et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Song, Xianzhou
Zhang, Chengwei
Zhao, Mingkun
Chen, Hui
Liu, Xing
Chen, Jianwei
Lonard, David M.
Qin, Li
Xu, Jianming
Wang, Xiaosong
Li, Feng
O’Malley, Bert W.
Wang, Jin
Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title_full Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title_fullStr Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title_full_unstemmed Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title_short Steroid Receptor Coactivator-3 (SRC-3/AIB1) as a Novel Therapeutic Target in Triple Negative Breast Cancer and Its Inhibition with a Phospho-Bufalin Prodrug
title_sort steroid receptor coactivator-3 (src-3/aib1) as a novel therapeutic target in triple negative breast cancer and its inhibition with a phospho-bufalin prodrug
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592245/
https://www.ncbi.nlm.nih.gov/pubmed/26431029
http://dx.doi.org/10.1371/journal.pone.0140011
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