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Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation
Synthetic lethality is a lethal phenomenon in which the occurrence of a single genetic event is tolerable for cell survival, whereas the co-occurrence of multiple genetic events results in cell death. The main obstacle for synthetic lethality lies in the tumor biology heterogeneity and complexity, t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470446/ https://www.ncbi.nlm.nih.gov/pubmed/32883316 http://dx.doi.org/10.1186/s13045-020-00956-5 |
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author | Topatana, Win Juengpanich, Sarun Li, Shijie Cao, Jiasheng Hu, Jiahao Lee, Jiyoung Suliyanto, Kenneth Ma, Diana Zhang, Bin Chen, Mingyu Cai, Xiujun |
author_facet | Topatana, Win Juengpanich, Sarun Li, Shijie Cao, Jiasheng Hu, Jiahao Lee, Jiyoung Suliyanto, Kenneth Ma, Diana Zhang, Bin Chen, Mingyu Cai, Xiujun |
author_sort | Topatana, Win |
collection | PubMed |
description | Synthetic lethality is a lethal phenomenon in which the occurrence of a single genetic event is tolerable for cell survival, whereas the co-occurrence of multiple genetic events results in cell death. The main obstacle for synthetic lethality lies in the tumor biology heterogeneity and complexity, the inadequate understanding of synthetic lethal interactions, drug resistance, and the challenges regarding screening and clinical translation. Recently, DNA damage response inhibitors are being tested in various trials with promising results. This review will describe the current challenges, development, and opportunities for synthetic lethality in cancer therapy. The characterization of potential synthetic lethal interactions and novel technologies to develop a more effective targeted drug for cancer patients will be explored. Furthermore, this review will discuss the clinical development and drug resistance mechanisms of synthetic lethality in cancer therapy. The ultimate goal of this review is to guide clinicians at selecting patients that will receive the maximum benefits of DNA damage response inhibitors for cancer therapy. |
format | Online Article Text |
id | pubmed-7470446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74704462020-09-08 Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation Topatana, Win Juengpanich, Sarun Li, Shijie Cao, Jiasheng Hu, Jiahao Lee, Jiyoung Suliyanto, Kenneth Ma, Diana Zhang, Bin Chen, Mingyu Cai, Xiujun J Hematol Oncol Review Synthetic lethality is a lethal phenomenon in which the occurrence of a single genetic event is tolerable for cell survival, whereas the co-occurrence of multiple genetic events results in cell death. The main obstacle for synthetic lethality lies in the tumor biology heterogeneity and complexity, the inadequate understanding of synthetic lethal interactions, drug resistance, and the challenges regarding screening and clinical translation. Recently, DNA damage response inhibitors are being tested in various trials with promising results. This review will describe the current challenges, development, and opportunities for synthetic lethality in cancer therapy. The characterization of potential synthetic lethal interactions and novel technologies to develop a more effective targeted drug for cancer patients will be explored. Furthermore, this review will discuss the clinical development and drug resistance mechanisms of synthetic lethality in cancer therapy. The ultimate goal of this review is to guide clinicians at selecting patients that will receive the maximum benefits of DNA damage response inhibitors for cancer therapy. BioMed Central 2020-09-03 /pmc/articles/PMC7470446/ /pubmed/32883316 http://dx.doi.org/10.1186/s13045-020-00956-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Topatana, Win Juengpanich, Sarun Li, Shijie Cao, Jiasheng Hu, Jiahao Lee, Jiyoung Suliyanto, Kenneth Ma, Diana Zhang, Bin Chen, Mingyu Cai, Xiujun Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title | Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title_full | Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title_fullStr | Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title_full_unstemmed | Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title_short | Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
title_sort | advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470446/ https://www.ncbi.nlm.nih.gov/pubmed/32883316 http://dx.doi.org/10.1186/s13045-020-00956-5 |
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