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SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine
SATB2 (special AT-rich sequence-binding protein 2) is a member of the special AT-rich binding protein family. As a transcription regulator, SATB2 mainly integrates higher-order chromatin organization. SATB2 expression appears to be tissue- and stage-specific, and is governed by several cellular sign...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chongqing Medical University
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720659/ https://www.ncbi.nlm.nih.gov/pubmed/35005110 http://dx.doi.org/10.1016/j.gendis.2020.10.003 |
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author | Huang, Xia Chen, Qiuman Luo, Wenping Pakvasa, Mikhail Zhang, Yuxin Zheng, Liwen Li, Shuang Yang, Zhuohui Zeng, Huan Liang, Fang Zhang, Fugui Hu, Daniel A. Qin, Kevin H. Wang, Eric J. Qin, David S. Reid, Russell R. He, Tong-Chuan Athiviraham, Aravind El Dafrawy, Mostafa Zhang, Hongmei |
author_facet | Huang, Xia Chen, Qiuman Luo, Wenping Pakvasa, Mikhail Zhang, Yuxin Zheng, Liwen Li, Shuang Yang, Zhuohui Zeng, Huan Liang, Fang Zhang, Fugui Hu, Daniel A. Qin, Kevin H. Wang, Eric J. Qin, David S. Reid, Russell R. He, Tong-Chuan Athiviraham, Aravind El Dafrawy, Mostafa Zhang, Hongmei |
author_sort | Huang, Xia |
collection | PubMed |
description | SATB2 (special AT-rich sequence-binding protein 2) is a member of the special AT-rich binding protein family. As a transcription regulator, SATB2 mainly integrates higher-order chromatin organization. SATB2 expression appears to be tissue- and stage-specific, and is governed by several cellular signaling molecules and mediators. Expressed in branchial arches and osteoblast-lineage cells, SATB2 plays a significant role in craniofacial pattern and skeleton development. In addition to regulating osteogenic differentiation, SATB2 also displays versatile functions in neural development and cancer progression. As an osteoinductive factor, SATB2 holds great promise in improving bone regeneration toward bone defect repair. In this review, we have summarized our current understanding of the physiological and pathological functions of SATB2 in craniofacial and skeleton development, neurogenesis, tumorigenesis and regenerative medicine. |
format | Online Article Text |
id | pubmed-8720659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Chongqing Medical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-87206592022-01-07 SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine Huang, Xia Chen, Qiuman Luo, Wenping Pakvasa, Mikhail Zhang, Yuxin Zheng, Liwen Li, Shuang Yang, Zhuohui Zeng, Huan Liang, Fang Zhang, Fugui Hu, Daniel A. Qin, Kevin H. Wang, Eric J. Qin, David S. Reid, Russell R. He, Tong-Chuan Athiviraham, Aravind El Dafrawy, Mostafa Zhang, Hongmei Genes Dis Review Article SATB2 (special AT-rich sequence-binding protein 2) is a member of the special AT-rich binding protein family. As a transcription regulator, SATB2 mainly integrates higher-order chromatin organization. SATB2 expression appears to be tissue- and stage-specific, and is governed by several cellular signaling molecules and mediators. Expressed in branchial arches and osteoblast-lineage cells, SATB2 plays a significant role in craniofacial pattern and skeleton development. In addition to regulating osteogenic differentiation, SATB2 also displays versatile functions in neural development and cancer progression. As an osteoinductive factor, SATB2 holds great promise in improving bone regeneration toward bone defect repair. In this review, we have summarized our current understanding of the physiological and pathological functions of SATB2 in craniofacial and skeleton development, neurogenesis, tumorigenesis and regenerative medicine. Chongqing Medical University 2020-10-17 /pmc/articles/PMC8720659/ /pubmed/35005110 http://dx.doi.org/10.1016/j.gendis.2020.10.003 Text en © 2020 Chongqing Medical University. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Huang, Xia Chen, Qiuman Luo, Wenping Pakvasa, Mikhail Zhang, Yuxin Zheng, Liwen Li, Shuang Yang, Zhuohui Zeng, Huan Liang, Fang Zhang, Fugui Hu, Daniel A. Qin, Kevin H. Wang, Eric J. Qin, David S. Reid, Russell R. He, Tong-Chuan Athiviraham, Aravind El Dafrawy, Mostafa Zhang, Hongmei SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title | SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title_full | SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title_fullStr | SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title_full_unstemmed | SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title_short | SATB2: A versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
title_sort | satb2: a versatile transcriptional regulator of craniofacial and skeleton development, neurogenesis and tumorigenesis, and its applications in regenerative medicine |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720659/ https://www.ncbi.nlm.nih.gov/pubmed/35005110 http://dx.doi.org/10.1016/j.gendis.2020.10.003 |
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