Application of the Yamanaka Transcription Factors Oct4, Sox2, Klf4, and c-Myc from the Laboratory to the Clinic

被引:17
|
作者
Aguirre, Marisol [1 ,2 ]
Escobar, Manuela [3 ]
Forero Amezquita, Sebastian [3 ]
Cubillos, David [3 ]
Rincon, Camilo [3 ]
Vanegas, Paula [3 ]
Tarazona, Maria Paula [3 ]
Atuesta Escobar, Sofia [3 ]
Blanco, Juan Camilo [3 ]
Celis, Luis Gustavo [3 ]
机构
[1] Fdn Valle Lili, Dept Genet, Cali 760026, Colombia
[2] Univ Icesi, Fac Med, Cali 760031, Colombia
[3] Univ Sabana, Fac Med, Km 7,Autopista Norte Bogota, Chia 250001, Colombia
关键词
cell- and tissue-based therapy; Oct4; Sox2; Klf4; c-Myc; cancer; neurodegenerative diseases; induced pluripotent stem cells; rejuvenation; PLURIPOTENT STEM-CELLS; HUMAN FIBROBLASTS; GENERATION; DIFFERENTIATION; MECHANISMS; INDUCTION; THERAPY; MOUSE; ALS;
D O I
10.3390/genes14091697
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The transcription factors Oct4, Sox2, Klf4, and c-Myc 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 Klf4 and c-Myc 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.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] Superoxide dismutase 1 expression is modulated by the core pluripotency transcription factors Oct4, Sox2 and Nanog in embryonic stem cells
    Solari, Claudia
    Victoria Petrone, Maria
    Vazquez Echegaray, Camila
    Soledad Cosentino, Maria
    Waisman, Ariel
    Francia, Marcos
    Baranao, Lino
    Miriuka, Santiago
    Guberman, Alejandra
    MECHANISMS OF DEVELOPMENT, 2018, 154 : 116 - 121
  • [32] The expression profile of Oct4 and Sox2 in the carcinogenesis of oral mucosa
    Qiao, Bin
    He, Baoxia
    Cai, Jinghua
    Yang, Wenli
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2014, 7 (01): : 28 - 37
  • [33] Oct4 and Sox2 are overexpressed in human neuroblastoma and inhibited by chemotherapy
    Yang, Shaobo
    Zheng, Jicui
    Ma, Yangyang
    Zhu, Haitao
    Xu, Ting
    Dong, Kuiran
    Xiao, Xianmin
    ONCOLOGY REPORTS, 2012, 28 (01) : 186 - 192
  • [34] Interplay of Oct4 with Sox2 and Sox17: a molecular switch from stem cell pluripotency to specifying a cardiac fate
    Stefanovic, Sonia
    Abboud, Nesrine
    Desilets, Stephanie
    Nury, David
    Cowan, Chad
    Puceat, Michel
    JOURNAL OF CELL BIOLOGY, 2009, 186 (05) : 665 - 673
  • [35] MicroRNA Replacing Oncogenic Klf4 and c-Myc for Generating iPS Cells via Cationized Pleurotus eryngii Polysaccharide-based Nanotransfection
    Deng, Wenwen
    Cao, Xia
    Chen, Jingjing
    Zhang, Zhijian
    Yu, Qingtong
    Wang, Yan
    Shao, Genbao
    Zhou, Jie
    Gao, Xiangdong
    Yu, Jiangnan
    Xu, Ximing
    ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (34) : 18957 - 18966
  • [36] Enhanced OCT4 transcriptional activity substitutes for exogenous SOX2 in cellular reprogramming
    Marthaler, Adele G.
    Adachi, Kenjiro
    Tiemann, Ulf
    Wu, Guangming
    Sabour, Davood
    Velychko, Sergiy
    Kleiter, Ingo
    Schoeler, Hans R.
    Tapia, Natalia
    SCIENTIFIC REPORTS, 2016, 6
  • [37] Comparison of Cellular Transforming Activity of OCT4, NANOG, and SOX2 in Immortalized Astrocytes
    Seo, Sunyoung
    Jeon, Hee-Young
    Kim, Hyunggee
    DNA AND CELL BIOLOGY, 2017, 36 (11) : 1000 - 1009
  • [38] Concomitant upregulation of nucleostemin and downregulation of Sox2 and Klf4 in gastric adenocarcinoma
    Asadi, Malek Hossein
    Derakhshani, Ali
    Mowla, Seyed Javad
    TUMOR BIOLOGY, 2014, 35 (07) : 7177 - 7185
  • [39] Rapid and efficient reprogramming of human amnion-derived cells into pluripotency by three factors OCT4/SOX2/NANOG
    Zhao, Hong-xi
    Li, Yang
    Jin, Hai-feng
    Xie, Li
    Liu, Chuang
    Jiang, Feng
    Luo, Ya-ning
    Yin, Guo-wu
    Li, Yi
    Wang, Jun
    Li, Ling-song
    Yao, Yuan-qing
    Wang, Xiao-hong
    DIFFERENTIATION, 2010, 80 (2-3) : 123 - 129
  • [40] Craniopharyngiomas Express Embryonic Stem Cell Markers (SOX2, OCT4, KLF4, and SOX9) as Pituitary Stem Cells but Do Not Coexpress RET/GFRA3 Receptors
    Garcia-Lavandeira, Montserrat
    Saez, Carmen
    Diaz-Rodriguez, Esther
    Perez-Romero, Sihara
    Senra, Ana
    Dieguez, Carlos
    Japon, Miguel A.
    Alvarez, Clara V.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (01) : E80 - E87