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山中因子 、 、 、 和 从实验室到临床的应用。

Application of the Yamanaka Transcription Factors , , , and from the Laboratory to the Clinic.

机构信息

Department of Genetics, Fundación Valle del Lili, Cali 760026, Colombia.

Faculty of Medicine, Universidad Icesi, Cali 760031, Colombia.

出版信息

Genes (Basel). 2023 Aug 26;14(9):1697. doi: 10.3390/genes14091697.


DOI:10.3390/genes14091697
PMID:37761837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10531188/
Abstract

The transcription factors , , , and enable the reprogramming of somatic cells into induced pluripotent cells. Reprogramming generates newly differentiated cells for potential therapies in cancer, neurodegenerative diseases, and rejuvenation processes. In cancer therapies, these transcription factors lead to a reduction in the size and aggressiveness of certain tumors, such as sarcomas, and in neurodegenerative diseases, they enable the production of dopaminergic cells in Parkinson's disease, the replacement of affected neuronal cells in olivopontocerebellar atrophy, and the regeneration of the optic nerve. However, there are limitations, such as an increased risk of cancer development when using and and the occurrence of abnormal dyskinesias in the medium term, possibly generated by the uncontrolled growth of differentiated dopaminergic cells and the impairment of the survival of the new cells. Therefore, the Yamanaka transcription factors have shown therapeutic potential through cell reprogramming for some carcinomas, neurodegenerative diseases, and rejuvenation. However, the limitations found in the studies require further investigation before the use of these transcription factors in humans.

摘要

转录因子 、 、 、 和 能够将体细胞重编程为诱导多能干细胞。重编程可产生新的分化细胞,用于癌症、神经退行性疾病和衰老过程的潜在治疗。在癌症治疗中,这些转录因子可导致某些肿瘤(如肉瘤)的大小和侵袭性降低,在神经退行性疾病中,它们可促使帕金森病中产生多巴胺能细胞,替代橄榄桥脑小脑萎缩中受影响的神经元细胞,并使视神经再生。然而,也存在一些限制,例如使用 和 时癌症发展风险增加,以及中期出现异常运动障碍,可能是由分化的多巴胺能细胞不受控制的生长和新细胞存活受损引起的。因此,Yamanaka 转录因子通过细胞重编程在一些癌症、神经退行性疾病和衰老方面显示出了治疗潜力。然而,在这些转录因子应用于人类之前,研究中发现的这些局限性需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/293512de125b/genes-14-01697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/f00a9dff45dc/genes-14-01697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/8fe2b4c189e6/genes-14-01697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/3b2dcb3cdca0/genes-14-01697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/293512de125b/genes-14-01697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/f00a9dff45dc/genes-14-01697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/8fe2b4c189e6/genes-14-01697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/3b2dcb3cdca0/genes-14-01697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec5/10531188/293512de125b/genes-14-01697-g004.jpg

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本文引用的文献

[1]
Gene Therapy-Mediated Partial Reprogramming Extends Lifespan and Reverses Age-Related Changes in Aged Mice.

Cell Reprogram. 2024-2

[2]
Generation of an induced pluripotent stem cell line SDPHi002-A from a patient with lung cancer.

Stem Cell Res. 2023-6

[3]
Induced Pluripotent Stem Cells and Their Applications in Amyotrophic Lateral Sclerosis.

Cells. 2023-3-22

[4]
Early Life Reprogramming-Based Treatment Promotes Longevity.

Cell Reprogram. 2023-2

[5]
Generation of neural organoids for spinal-cord regeneration via the direct reprogramming of human astrocytes.

Nat Biomed Eng. 2023-3

[6]
Age reprogramming: cell rejuvenation by partial reprogramming.

Development. 2022-11-15

[7]
Amyotrophic lateral sclerosis.

Lancet. 2022-10-15

[8]
CHD4 mediates SOX2 transcription through TRPS1 in luminal breast cancer.

Cell Signal. 2022-12

[9]
SOX2 regulates paclitaxel resistance of A549 non‑small cell lung cancer cells via promoting transcription of ClC‑3.

Oncol Rep. 2022-10

[10]
Induced neural stem cells from Macaca fascicularis show potential of dopaminergic neuron specification and efficacy in a mouse Parkinson's disease model.

Acta Histochem. 2022-8

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