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Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies
Bringing to a halt the cell cycle in mitosis and interfering with its normal progression is one of the most successful anti-cancer strategies used nowadays. Classically, several kinds of anti-cancer drugs like taxanes and vinca alkaloids directly inhibit microtubules during cell division. These drug...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890118/ https://www.ncbi.nlm.nih.gov/pubmed/35251692 http://dx.doi.org/10.2144/fsoa-2021-0116 |
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author | Shahin, Rand Aljamal, Salah |
author_facet | Shahin, Rand Aljamal, Salah |
author_sort | Shahin, Rand |
collection | PubMed |
description | Bringing to a halt the cell cycle in mitosis and interfering with its normal progression is one of the most successful anti-cancer strategies used nowadays. Classically, several kinds of anti-cancer drugs like taxanes and vinca alkaloids directly inhibit microtubules during cell division. These drugs exhibit serious side effects, most importantly, severe peripheral neuropathies. Alternatively, KSP inhibitors are grasping a lot of research attention as less toxic mitotic inhibitors. In this review, we track the medicinal chemistry developmental stages of KSP inhibitors. Moreover, we address the challenges that are faced during the development of KSP inhibitor therapy for cancer and future insights for the latest advances in research that are directed to find active KSP inhibitor drugs. |
format | Online Article Text |
id | pubmed-8890118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88901182022-03-04 Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies Shahin, Rand Aljamal, Salah Future Sci OA Review Bringing to a halt the cell cycle in mitosis and interfering with its normal progression is one of the most successful anti-cancer strategies used nowadays. Classically, several kinds of anti-cancer drugs like taxanes and vinca alkaloids directly inhibit microtubules during cell division. These drugs exhibit serious side effects, most importantly, severe peripheral neuropathies. Alternatively, KSP inhibitors are grasping a lot of research attention as less toxic mitotic inhibitors. In this review, we track the medicinal chemistry developmental stages of KSP inhibitors. Moreover, we address the challenges that are faced during the development of KSP inhibitor therapy for cancer and future insights for the latest advances in research that are directed to find active KSP inhibitor drugs. Future Science Ltd 2022-02-21 /pmc/articles/PMC8890118/ /pubmed/35251692 http://dx.doi.org/10.2144/fsoa-2021-0116 Text en © 2022 Dr Rand Omar Shahin https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Review Shahin, Rand Aljamal, Salah Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title | Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title_full | Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title_fullStr | Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title_full_unstemmed | Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title_short | Kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
title_sort | kinesin spindle protein inhibitors in cancer: from high throughput screening to novel therapeutic strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890118/ https://www.ncbi.nlm.nih.gov/pubmed/35251692 http://dx.doi.org/10.2144/fsoa-2021-0116 |
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