Retinal determination gene networks: from biological functions to therapeutic strategies

被引:0
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作者
Shuangli Zhu
Wanling Li
Hao Zhang
Yuheng Yan
Qi Mei
Kongming Wu
机构
[1] Tongji Hospital of Tongji Medical College,Department of Oncology
[2] Huazhong University of Science and Technology,Department of Geriatrics
[3] Tongji Hospital of Tongji Medical College,Cancer Center
[4] Huazhong University of Science and Technology,Cancer Center
[5] Shanxi Bethune Hospital,undefined
[6] Shanxi Academy of Medical Science,undefined
[7] Tongji Shanxi Hospital,undefined
[8] Third Hospital of Shanxi Medical University,undefined
[9] Tongji hospital of Tongji Medical College,undefined
[10] Huazhong University of Science and Technology,undefined
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关键词
The retinal determinant gene network; DACH1; SIX1; EYA1; Cancer; Chronic kidney disease; Coronary artery disease; Organ development;
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摘要
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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