Focal adhesion kinase inhibitors, a heavy punch to cancer
Abstract Kinases are the ideal druggable targets for diseases and especially were highlighted on cancer therapy. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase and its aberrant signaling extensively implicates in the progression of most cancer types, involving in cancer cell growth, a...
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2021
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oai:doaj.org-article:f8375424d64f46afbf8002a1c77b3cca2021-11-28T12:42:05ZFocal adhesion kinase inhibitors, a heavy punch to cancer10.1007/s12672-021-00449-y2730-6011https://doaj.org/article/f8375424d64f46afbf8002a1c77b3cca2021-11-01T00:00:00Zhttps://doi.org/10.1007/s12672-021-00449-yhttps://doaj.org/toc/2730-6011Abstract Kinases are the ideal druggable targets for diseases and especially were highlighted on cancer therapy. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase and its aberrant signaling extensively implicates in the progression of most cancer types, involving in cancer cell growth, adhesion, migration, and tumor microenvironment (TME) remodeling. FAK is commonly overexpressed and activated in a variety of cancers and plays as a targetable kinase in cancer therapy. FAK inhibitors already exhibited promising performance in preclinical and early-stage clinical trials. Moreover, substantial evidence has implied that targeting FAK is more effective in combination strategy, thereby reversing the failure of chemotherapies or targeted therapies in solid tumors. In the current review, we summarized the drug development progress, chemotherapy strategy, and perspective view for FAK inhibitors.Yueling WuNing LiChengfeng YeXingmei JiangHui LuoBaoyuan ZhangYing ZhangQingyu ZhangSpringerarticleFocal adhesion kinaseFAK inhibitorsCancer chemotherapyNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENDiscover Oncology, Vol 12, Iss 1, Pp 1-15 (2021) |
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Focal adhesion kinase FAK inhibitors Cancer chemotherapy Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Focal adhesion kinase FAK inhibitors Cancer chemotherapy Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Yueling Wu Ning Li Chengfeng Ye Xingmei Jiang Hui Luo Baoyuan Zhang Ying Zhang Qingyu Zhang Focal adhesion kinase inhibitors, a heavy punch to cancer |
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Abstract Kinases are the ideal druggable targets for diseases and especially were highlighted on cancer therapy. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase and its aberrant signaling extensively implicates in the progression of most cancer types, involving in cancer cell growth, adhesion, migration, and tumor microenvironment (TME) remodeling. FAK is commonly overexpressed and activated in a variety of cancers and plays as a targetable kinase in cancer therapy. FAK inhibitors already exhibited promising performance in preclinical and early-stage clinical trials. Moreover, substantial evidence has implied that targeting FAK is more effective in combination strategy, thereby reversing the failure of chemotherapies or targeted therapies in solid tumors. In the current review, we summarized the drug development progress, chemotherapy strategy, and perspective view for FAK inhibitors. |
format |
article |
author |
Yueling Wu Ning Li Chengfeng Ye Xingmei Jiang Hui Luo Baoyuan Zhang Ying Zhang Qingyu Zhang |
author_facet |
Yueling Wu Ning Li Chengfeng Ye Xingmei Jiang Hui Luo Baoyuan Zhang Ying Zhang Qingyu Zhang |
author_sort |
Yueling Wu |
title |
Focal adhesion kinase inhibitors, a heavy punch to cancer |
title_short |
Focal adhesion kinase inhibitors, a heavy punch to cancer |
title_full |
Focal adhesion kinase inhibitors, a heavy punch to cancer |
title_fullStr |
Focal adhesion kinase inhibitors, a heavy punch to cancer |
title_full_unstemmed |
Focal adhesion kinase inhibitors, a heavy punch to cancer |
title_sort |
focal adhesion kinase inhibitors, a heavy punch to cancer |
publisher |
Springer |
publishDate |
2021 |
url |
https://doaj.org/article/f8375424d64f46afbf8002a1c77b3cca |
work_keys_str_mv |
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1718407869720690688 |