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Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy

Current cancer therapies have encountered adverse response due to poor therapeutic efficiency, severe side effects and acquired resistance to multiple drugs. Thus, there are urgent needs for finding new cancer-targeted pharmacological strategies. In this review, we summarized the current understandi...

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Detalles Bibliográficos
Autores principales: Li, Bin-Bin, Wang, Bo, Zhu, Cheng-Ming, Tang, Di, Pang, Jun, Zhao, Jing, Sun, Chun-Hui, Qiu, Miao-Juan, Qian, Zhi-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Medical Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926117/
https://www.ncbi.nlm.nih.gov/pubmed/31891127
http://dx.doi.org/10.1016/j.cdtm.2019.08.006
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author Li, Bin-Bin
Wang, Bo
Zhu, Cheng-Ming
Tang, Di
Pang, Jun
Zhao, Jing
Sun, Chun-Hui
Qiu, Miao-Juan
Qian, Zhi-Rong
author_facet Li, Bin-Bin
Wang, Bo
Zhu, Cheng-Ming
Tang, Di
Pang, Jun
Zhao, Jing
Sun, Chun-Hui
Qiu, Miao-Juan
Qian, Zhi-Rong
author_sort Li, Bin-Bin
collection PubMed
description Current cancer therapies have encountered adverse response due to poor therapeutic efficiency, severe side effects and acquired resistance to multiple drugs. Thus, there are urgent needs for finding new cancer-targeted pharmacological strategies. In this review, we summarized the current understanding with THZ1, a covalent inhibitor of cyclin-dependent kinase 7 (CDK7), which demonstrated promising anti-tumor activity against different cancer types. By introducing the anti-tumor behaviors and the potential targets for different cancers, this review aims to provide more effective approaches to CDK7 inhibitor-based therapeutic agents and deeper insight into the diverse tumor proliferation mechanisms.
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spelling pubmed-69261172019-12-30 Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy Li, Bin-Bin Wang, Bo Zhu, Cheng-Ming Tang, Di Pang, Jun Zhao, Jing Sun, Chun-Hui Qiu, Miao-Juan Qian, Zhi-Rong Chronic Dis Transl Med Perspective Current cancer therapies have encountered adverse response due to poor therapeutic efficiency, severe side effects and acquired resistance to multiple drugs. Thus, there are urgent needs for finding new cancer-targeted pharmacological strategies. In this review, we summarized the current understanding with THZ1, a covalent inhibitor of cyclin-dependent kinase 7 (CDK7), which demonstrated promising anti-tumor activity against different cancer types. By introducing the anti-tumor behaviors and the potential targets for different cancers, this review aims to provide more effective approaches to CDK7 inhibitor-based therapeutic agents and deeper insight into the diverse tumor proliferation mechanisms. Chinese Medical Association 2019-10-18 /pmc/articles/PMC6926117/ /pubmed/31891127 http://dx.doi.org/10.1016/j.cdtm.2019.08.006 Text en © 2019 Chinese Medical Association. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Perspective
Li, Bin-Bin
Wang, Bo
Zhu, Cheng-Ming
Tang, Di
Pang, Jun
Zhao, Jing
Sun, Chun-Hui
Qiu, Miao-Juan
Qian, Zhi-Rong
Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title_full Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title_fullStr Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title_full_unstemmed Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title_short Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy
title_sort cyclin-dependent kinase 7 inhibitor thz1 in cancer therapy
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926117/
https://www.ncbi.nlm.nih.gov/pubmed/31891127
http://dx.doi.org/10.1016/j.cdtm.2019.08.006
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