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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...

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Autores principales: Shahin, Rand, Aljamal, Salah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2022
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.
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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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