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Targeting DNA binding proteins for cancer therapy

Dysregulation or mutation of DNA binding proteins such as transcription factors (TFs) is associated with the onset and progression of various types of disease, including cancer. Alteration of TF activity occurs in numerous cancer tissues due to gene amplification, deletion, and point mutations, and...

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Detalles Bibliográficos
Autores principales: Shiroma, Yoshitomo, Takahashi, Ryou‐u, Yamamoto, Yuki, Tahara, Hidetoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156841/
https://www.ncbi.nlm.nih.gov/pubmed/32073717
http://dx.doi.org/10.1111/cas.14355
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author Shiroma, Yoshitomo
Takahashi, Ryou‐u
Yamamoto, Yuki
Tahara, Hidetoshi
author_facet Shiroma, Yoshitomo
Takahashi, Ryou‐u
Yamamoto, Yuki
Tahara, Hidetoshi
author_sort Shiroma, Yoshitomo
collection PubMed
description Dysregulation or mutation of DNA binding proteins such as transcription factors (TFs) is associated with the onset and progression of various types of disease, including cancer. Alteration of TF activity occurs in numerous cancer tissues due to gene amplification, deletion, and point mutations, and epigenetic modification. Although cancer‐associated TFs are promising targets for cancer therapy, development of drugs targeting these TFs has historically been difficult due to the lack of high‐throughput screening methods. Recent advances in technology for identification and selective inhibition of DNA binding proteins enable cancer researchers to develop novel therapeutics targeting cancer‐associated TFs. In the present review, we summarize known cancer‐associated TFs according to cancer type and introduce recently developed high‐throughput approaches to identify selective inhibitors of cancer‐associated TFs.
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spelling pubmed-71568412020-04-20 Targeting DNA binding proteins for cancer therapy Shiroma, Yoshitomo Takahashi, Ryou‐u Yamamoto, Yuki Tahara, Hidetoshi Cancer Sci Review Articles Dysregulation or mutation of DNA binding proteins such as transcription factors (TFs) is associated with the onset and progression of various types of disease, including cancer. Alteration of TF activity occurs in numerous cancer tissues due to gene amplification, deletion, and point mutations, and epigenetic modification. Although cancer‐associated TFs are promising targets for cancer therapy, development of drugs targeting these TFs has historically been difficult due to the lack of high‐throughput screening methods. Recent advances in technology for identification and selective inhibition of DNA binding proteins enable cancer researchers to develop novel therapeutics targeting cancer‐associated TFs. In the present review, we summarize known cancer‐associated TFs according to cancer type and introduce recently developed high‐throughput approaches to identify selective inhibitors of cancer‐associated TFs. John Wiley and Sons Inc. 2020-03-24 2020-04 /pmc/articles/PMC7156841/ /pubmed/32073717 http://dx.doi.org/10.1111/cas.14355 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Shiroma, Yoshitomo
Takahashi, Ryou‐u
Yamamoto, Yuki
Tahara, Hidetoshi
Targeting DNA binding proteins for cancer therapy
title Targeting DNA binding proteins for cancer therapy
title_full Targeting DNA binding proteins for cancer therapy
title_fullStr Targeting DNA binding proteins for cancer therapy
title_full_unstemmed Targeting DNA binding proteins for cancer therapy
title_short Targeting DNA binding proteins for cancer therapy
title_sort targeting dna binding proteins for cancer therapy
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156841/
https://www.ncbi.nlm.nih.gov/pubmed/32073717
http://dx.doi.org/10.1111/cas.14355
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