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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Medical Association
2019
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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. |
format | Online Article Text |
id | pubmed-6926117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Chinese Medical Association |
record_format | MEDLINE/PubMed |
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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