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Sox 转录因子家族:多能调节干细胞和祖细胞命运的因子。

The sox family of transcription factors: versatile regulators of stem and progenitor cell fate.

机构信息

Howard Hughes Medical Institute at Massachusetts General Hospital Cancer Center and Center for Regenerative Medicine, Boston, MA 02114, USA.

出版信息

Cell Stem Cell. 2013 Jan 3;12(1):15-30. doi: 10.1016/j.stem.2012.12.007.

DOI:10.1016/j.stem.2012.12.007
PMID:23290134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3608206/
Abstract

Sox family transcription factors are well-established regulators of cell fate decisions during development. Accumulating evidence documents that they play additional roles in adult tissue homeostasis and regeneration. Remarkably, forced expression of Sox factors, in combination with other synergistic factors, reprograms differentiated cells into somatic or pluripotent stem cells. Dysregulation of Sox factors has been further implicated in diseases including cancer. Here, we review molecular and functional evidence linking Sox proteins with stem cell biology, cellular reprogramming, and disease with an emphasis on Sox2.

摘要

Sox 家族转录因子是发育过程中细胞命运决定的重要调节因子。越来越多的证据表明,它们在成人组织稳态和再生中发挥额外的作用。值得注意的是,Sox 因子的强制表达,与其他协同因子结合,可将分化细胞重新编程为体干细胞或多能干细胞。Sox 因子的失调与包括癌症在内的疾病有关。在这里,我们回顾了 Sox 蛋白与干细胞生物学、细胞重编程和疾病的分子和功能证据,重点介绍 Sox2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/2ce0607d52a3/nihms-431222-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/7a3bdc7da44d/nihms-431222-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/46e6c84ea7b9/nihms-431222-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/e230cad540cb/nihms-431222-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/2ce0607d52a3/nihms-431222-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/7a3bdc7da44d/nihms-431222-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/46e6c84ea7b9/nihms-431222-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/e230cad540cb/nihms-431222-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ed9/3608206/2ce0607d52a3/nihms-431222-f0004.jpg

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Cell Stem Cell. 2013 Jan 3;12(1):88-100. doi: 10.1016/j.stem.2012.12.001. Epub 2012 Dec 20.
2
p27(Kip1) directly represses Sox2 during embryonic stem cell differentiation.p27(Kip1) 在胚胎干细胞分化过程中直接抑制 Sox2。
Cell Stem Cell. 2012 Dec 7;11(6):845-52. doi: 10.1016/j.stem.2012.09.014.
3
MEF promotes stemness in the pathogenesis of gliomas.
SOX2利用FOXA1作为异源转录伙伴来驱动去势抵抗性前列腺癌的增殖。
bioRxiv. 2025 Jul 19:2025.07.18.664790. doi: 10.1101/2025.07.18.664790.
4
TOX, through a glass, darkly.透过玻璃,隐约地看到“毒素”。
Front Immunol. 2025 Jul 17;16:1576468. doi: 10.3389/fimmu.2025.1576468. eCollection 2025.
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Biomolecules. 2025 Jul 18;15(7):1048. doi: 10.3390/biom15071048.
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TREM1 is essential for maintaining stemness of liver cancer stem-like cells in hepatocellular carcinoma.触发受体表达于髓系细胞-1(TREM1)对于维持肝细胞癌中肝癌干细胞样细胞的干性至关重要。
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