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Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer

Triple-negative breast cancer (TNBC) cells lack the expression of ER, PR and HER2. Thus, TNBC patients cannot benefit from hormone receptor-targeted therapy as non-TNBC patients, but can only receive chemotherapy as the systemic treatment and have a worse overall outcome. More effective therapeutic...

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Autores principales: Yu, Yong, Qi, Jingjing, Xiong, Jieyi, Jiang, Liping, Cui, Di, He, Junlin, Chen, Ping, Li, Lianjie, Wu, Chenjie, Ma, Tonghui, Shao, Su, Wang, Jianjun, Yu, Dansong, Zhou, Bing, Huang, Dongsheng, Schmitt, Clemens A., Tao, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376470/
https://www.ncbi.nlm.nih.gov/pubmed/30809307
http://dx.doi.org/10.7150/thno.29520
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author Yu, Yong
Qi, Jingjing
Xiong, Jieyi
Jiang, Liping
Cui, Di
He, Junlin
Chen, Ping
Li, Lianjie
Wu, Chenjie
Ma, Tonghui
Shao, Su
Wang, Jianjun
Yu, Dansong
Zhou, Bing
Huang, Dongsheng
Schmitt, Clemens A.
Tao, Ran
author_facet Yu, Yong
Qi, Jingjing
Xiong, Jieyi
Jiang, Liping
Cui, Di
He, Junlin
Chen, Ping
Li, Lianjie
Wu, Chenjie
Ma, Tonghui
Shao, Su
Wang, Jianjun
Yu, Dansong
Zhou, Bing
Huang, Dongsheng
Schmitt, Clemens A.
Tao, Ran
author_sort Yu, Yong
collection PubMed
description Triple-negative breast cancer (TNBC) cells lack the expression of ER, PR and HER2. Thus, TNBC patients cannot benefit from hormone receptor-targeted therapy as non-TNBC patients, but can only receive chemotherapy as the systemic treatment and have a worse overall outcome. More effective therapeutic targets and combination therapy strategies are urgently needed to improve the treatment effectiveness. Methods: We analyzed the expression levels of EZH2 and TET1 in TCGA and our own breast cancer patient cohort, and tested their correlation with patient survival. We used TNBC and non-TNBC cell lines and mouse xenograft tumor model to unveil novel EZH2 targets and investigated the effect of EZH2 inhibition or TET1 overexpression in cell proliferation and viability of TNBC cells. Results: In TNBC cells, EZH2 decreases TET1 expression by H3K27me3 epigenetic regulation and subsequently suppresses anti-tumor p53 signaling pathway. Patients with high EZH2 and low TET1 presented the poorest survival outcome. Experimentally, targeting EZH2 in TNBC cells with specific inhibitor GSK343 or shRNA genetic approach could induce cell cycle arrest and senescence by elevating TET1 expression and p53 pathway activation. Using mouse xenograft model, we have tested a novel therapy strategy to combine GSK343 and chemotherapy drug Adriamycin and could show drastic and robust inhibition of TNBC tumor growth by synergistic induction of senescence and apoptosis. Conclusions: We postulate that the well-controlled dynamic pathway EZH2-H3K27me3-TET1 is a novel epigenetic co-regulator module and provide evidence regarding how to exploit it as a novel therapeutic target via its pivotal role in senescence and apoptosis control. Of clinical and therapeutic significance, the present study opens a new avenue for TNBC treatment by targeting the EZH2-H3K27me3-TET1 pathway that can modulate the epigenetic landscape.
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spelling pubmed-63764702019-02-26 Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer Yu, Yong Qi, Jingjing Xiong, Jieyi Jiang, Liping Cui, Di He, Junlin Chen, Ping Li, Lianjie Wu, Chenjie Ma, Tonghui Shao, Su Wang, Jianjun Yu, Dansong Zhou, Bing Huang, Dongsheng Schmitt, Clemens A. Tao, Ran Theranostics Research Paper Triple-negative breast cancer (TNBC) cells lack the expression of ER, PR and HER2. Thus, TNBC patients cannot benefit from hormone receptor-targeted therapy as non-TNBC patients, but can only receive chemotherapy as the systemic treatment and have a worse overall outcome. More effective therapeutic targets and combination therapy strategies are urgently needed to improve the treatment effectiveness. Methods: We analyzed the expression levels of EZH2 and TET1 in TCGA and our own breast cancer patient cohort, and tested their correlation with patient survival. We used TNBC and non-TNBC cell lines and mouse xenograft tumor model to unveil novel EZH2 targets and investigated the effect of EZH2 inhibition or TET1 overexpression in cell proliferation and viability of TNBC cells. Results: In TNBC cells, EZH2 decreases TET1 expression by H3K27me3 epigenetic regulation and subsequently suppresses anti-tumor p53 signaling pathway. Patients with high EZH2 and low TET1 presented the poorest survival outcome. Experimentally, targeting EZH2 in TNBC cells with specific inhibitor GSK343 or shRNA genetic approach could induce cell cycle arrest and senescence by elevating TET1 expression and p53 pathway activation. Using mouse xenograft model, we have tested a novel therapy strategy to combine GSK343 and chemotherapy drug Adriamycin and could show drastic and robust inhibition of TNBC tumor growth by synergistic induction of senescence and apoptosis. Conclusions: We postulate that the well-controlled dynamic pathway EZH2-H3K27me3-TET1 is a novel epigenetic co-regulator module and provide evidence regarding how to exploit it as a novel therapeutic target via its pivotal role in senescence and apoptosis control. Of clinical and therapeutic significance, the present study opens a new avenue for TNBC treatment by targeting the EZH2-H3K27me3-TET1 pathway that can modulate the epigenetic landscape. Ivyspring International Publisher 2019-01-24 /pmc/articles/PMC6376470/ /pubmed/30809307 http://dx.doi.org/10.7150/thno.29520 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Yu, Yong
Qi, Jingjing
Xiong, Jieyi
Jiang, Liping
Cui, Di
He, Junlin
Chen, Ping
Li, Lianjie
Wu, Chenjie
Ma, Tonghui
Shao, Su
Wang, Jianjun
Yu, Dansong
Zhou, Bing
Huang, Dongsheng
Schmitt, Clemens A.
Tao, Ran
Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title_full Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title_fullStr Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title_full_unstemmed Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title_short Epigenetic Co-Deregulation of EZH2/TET1 is a Senescence-Countering, Actionable Vulnerability in Triple-Negative Breast Cancer
title_sort epigenetic co-deregulation of ezh2/tet1 is a senescence-countering, actionable vulnerability in triple-negative breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376470/
https://www.ncbi.nlm.nih.gov/pubmed/30809307
http://dx.doi.org/10.7150/thno.29520
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