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The UPF1 RNA Surveillance Gene is Commonly Mutated in Pancreatic Adenosquamous Carcinoma

Pancreatic adenosquamous carcinoma (ASC) is an enigmatic and aggressive tumor that has a worse prognosis and higher metastatic potential than its adenocarcinoma counterpart. Here we report that ASC tumors frequently harbor somatically acquired mutations in the UPF1 gene, which encodes the core compo...

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Detalles Bibliográficos
Autores principales: Liu, Chen, Karam, Rachid, Zhou, YingQi, Su, Fang, Ji, Yuan, Li, Gang, Xu, GuoTong, Lu, LiXia, Wang, ChongRen, Song, MeiYi, Zhu, JingPing, Wang, YiRan, Zhao, YiFan, Foo, Wai Chin, Zuo, Mingxin, Valasek, Mark A, Javle, Milind, Wilkinson, Miles F, Lu, YanJun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048332/
https://www.ncbi.nlm.nih.gov/pubmed/24859531
http://dx.doi.org/10.1038/nm.3548
Descripción
Sumario:Pancreatic adenosquamous carcinoma (ASC) is an enigmatic and aggressive tumor that has a worse prognosis and higher metastatic potential than its adenocarcinoma counterpart. Here we report that ASC tumors frequently harbor somatically acquired mutations in the UPF1 gene, which encodes the core component of the nonsense-mediated RNA decay (NMD) pathway. These tumor-specific mutations alter UPF1 RNA splicing and perturb NMD, leading to upregulated levels of NMD substrate mRNAs. UPF1 mutations are the first known unique molecular signatures of ASC.