Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignancies

The RB1 gene is frequently mutated in human cancers but its role in tumorigenesis remains incompletely defined. Using an induced pluripotent stem cell (iPSC) model of hereditary retinoblastoma (RB), we report that the spliceosome is an up-regulated target responding to oncogenic stress in RB1-mutant...

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Detalles Bibliográficos
Autores principales: Tu, Jian, Huo, Zijun, Yu, Yao, Zhu, Dandan, Xu, An, Huang, Mo-Fan, Hu, Ruifeng, Wang, Ruoyu, Gingold, Julian A., Chen, Yi-Hung, Tsai, Kuang-Lei, Forcioli-Conti, Nicolas R., Huang, Sarah X. L., Webb, Thomas R., Su, Jie, Bazer, Danielle A., Jia, Peilin, Yustein, Jason T., Wang, Lisa L., Hung, Mien-Chie, Zhao, Zhongming, Huff, Chad D., Shen, Jingnan, Zhao, Ruiying, Lee, Dung-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Biological Sciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169787/
https://www.ncbi.nlm.nih.gov/pubmed/35412907
http://dx.doi.org/10.1073/pnas.2117857119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169787/
https://www.ncbi.nlm.nih.gov/pubmed/35412907
http://dx.doi.org/10.1073/pnas.2117857119

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