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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KeAi Communications Co., Ltd.
2019
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oai:doaj.org-article:c65a4a41082d4663a0cc81b8d4f5703e2021-12-02T11:52:55ZCyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy2095-882X10.1016/j.cdtm.2019.08.006https://doaj.org/article/c65a4a41082d4663a0cc81b8d4f5703e2019-09-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2095882X19300714https://doaj.org/toc/2095-882XCurrent 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. Keywords: THZ1, Cyclin-dependent kinase 7, Cancer therapy, Transcription, Super-enhancerBin-Bin LiBo WangCheng-Ming ZhuDi TangJun PangJing ZhaoChun-Hui SunMiao-Juan QiuZhi-Rong QianKeAi Communications Co., Ltd.articleMedicine (General)R5-920ENChronic Diseases and Translational Medicine, Vol 5, Iss 3, Pp 155-169 (2019) |
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DOAJ |
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Medicine (General) R5-920 |
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Medicine (General) R5-920 Bin-Bin Li Bo Wang Cheng-Ming Zhu Di Tang Jun Pang Jing Zhao Chun-Hui Sun Miao-Juan Qiu Zhi-Rong Qian Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy |
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. Keywords: THZ1, Cyclin-dependent kinase 7, Cancer therapy, Transcription, Super-enhancer |
format |
article |
author |
Bin-Bin Li Bo Wang Cheng-Ming Zhu Di Tang Jun Pang Jing Zhao Chun-Hui Sun Miao-Juan Qiu Zhi-Rong Qian |
author_facet |
Bin-Bin Li Bo Wang Cheng-Ming Zhu Di Tang Jun Pang Jing Zhao Chun-Hui Sun Miao-Juan Qiu Zhi-Rong Qian |
author_sort |
Bin-Bin Li |
title |
Cyclin-dependent kinase 7 inhibitor THZ1 in cancer therapy |
title_short |
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_sort |
cyclin-dependent kinase 7 inhibitor thz1 in cancer therapy |
publisher |
KeAi Communications Co., Ltd. |
publishDate |
2019 |
url |
https://doaj.org/article/c65a4a41082d4663a0cc81b8d4f5703e |
work_keys_str_mv |
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1718394951640809472 |