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Retinal determination gene networks: from biological functions to therapeutic strategies

The retinal determinant gene network (RDGN), originally discovered as a critical determinator in Drosophila eye specification, has become an important regulatory network in tumorigenesis and progression, as well as organogenesis. This network is not only associated with malignant biological behavior...

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Autores principales: Zhu, Shuangli, Li, Wanling, Zhang, Hao, Yan, Yuheng, Mei, Qi, Wu, Kongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906957/
https://www.ncbi.nlm.nih.gov/pubmed/36750914
http://dx.doi.org/10.1186/s40364-023-00459-8
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author Zhu, Shuangli
Li, Wanling
Zhang, Hao
Yan, Yuheng
Mei, Qi
Wu, Kongming
author_facet Zhu, Shuangli
Li, Wanling
Zhang, Hao
Yan, Yuheng
Mei, Qi
Wu, Kongming
author_sort Zhu, Shuangli
collection PubMed
description The retinal determinant gene network (RDGN), originally discovered as a critical determinator in Drosophila eye specification, has become an important regulatory network in tumorigenesis and progression, as well as organogenesis. This network is not only associated with malignant biological behaviors of tumors, such as proliferation, and invasion, but also regulates the development of multiple mammalian organs. Three members of this conservative network have been extensively investigated, including DACH, SIX, and EYA. Dysregulated RDGN signaling is associated with the initiation and progression of tumors. In recent years, it has been found that the members of this network can be used as prognostic markers for cancer patients. Moreover, they are considered to be potential therapeutic targets for cancer. Here, we summarize the research progress of RDGN members from biological functions to signaling transduction, especially emphasizing their effects on tumors. Additionally, we discuss the roles of RDGN members in the development of organs and tissue as well as their correlations with the pathogenesis of chronic kidney disease and coronary heart disease. By summarizing the roles of RDGN members in human diseases, we hope to promote future investigations into RDGN and provide potential therapeutic strategies for patients.
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spelling pubmed-99069572023-02-08 Retinal determination gene networks: from biological functions to therapeutic strategies Zhu, Shuangli Li, Wanling Zhang, Hao Yan, Yuheng Mei, Qi Wu, Kongming Biomark Res Review The retinal determinant gene network (RDGN), originally discovered as a critical determinator in Drosophila eye specification, has become an important regulatory network in tumorigenesis and progression, as well as organogenesis. This network is not only associated with malignant biological behaviors of tumors, such as proliferation, and invasion, but also regulates the development of multiple mammalian organs. Three members of this conservative network have been extensively investigated, including DACH, SIX, and EYA. Dysregulated RDGN signaling is associated with the initiation and progression of tumors. In recent years, it has been found that the members of this network can be used as prognostic markers for cancer patients. Moreover, they are considered to be potential therapeutic targets for cancer. Here, we summarize the research progress of RDGN members from biological functions to signaling transduction, especially emphasizing their effects on tumors. Additionally, we discuss the roles of RDGN members in the development of organs and tissue as well as their correlations with the pathogenesis of chronic kidney disease and coronary heart disease. By summarizing the roles of RDGN members in human diseases, we hope to promote future investigations into RDGN and provide potential therapeutic strategies for patients. BioMed Central 2023-02-08 /pmc/articles/PMC9906957/ /pubmed/36750914 http://dx.doi.org/10.1186/s40364-023-00459-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Zhu, Shuangli
Li, Wanling
Zhang, Hao
Yan, Yuheng
Mei, Qi
Wu, Kongming
Retinal determination gene networks: from biological functions to therapeutic strategies
title Retinal determination gene networks: from biological functions to therapeutic strategies
title_full Retinal determination gene networks: from biological functions to therapeutic strategies
title_fullStr Retinal determination gene networks: from biological functions to therapeutic strategies
title_full_unstemmed Retinal determination gene networks: from biological functions to therapeutic strategies
title_short Retinal determination gene networks: from biological functions to therapeutic strategies
title_sort retinal determination gene networks: from biological functions to therapeutic strategies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906957/
https://www.ncbi.nlm.nih.gov/pubmed/36750914
http://dx.doi.org/10.1186/s40364-023-00459-8
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