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A method to establish a c-Myc transgenic mouse model of hepatocellular carcinoma

Hepatocellular carcinoma (HCC) remains one of the most lethal malignant cancers worldwide. HCC mouse models are widely used to explore the molecular pathogenesis of HCC and to test novel drug candidates. The advantages of this mouse model are as follows: • This method developed a H11(LNL-Myc) knock-...

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Detalles Bibliográficos
Autores principales: Mei, Yan, Zhou, Chao, Liang, Chao-Yong, Lu, Guan-Ming, Zeng, Mu-Sheng, Wang, Jin-Jin, Feng, Guo-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256637/
https://www.ncbi.nlm.nih.gov/pubmed/32489910
http://dx.doi.org/10.1016/j.mex.2020.100921
Descripción
Sumario:Hepatocellular carcinoma (HCC) remains one of the most lethal malignant cancers worldwide. HCC mouse models are widely used to explore the molecular pathogenesis of HCC and to test novel drug candidates. The advantages of this mouse model are as follows: • This method developed a H11(LNL-Myc) knock-in HCC mouse model by crossing H11(LNL-Myc) heterozygous mice with (albumin (Alb))-cre transgenic mice to generate c-Myc/Alb-cre double positive mice. • The c-Myc/Alb-cre double-positive mice exhibited a typical HCC phenotype, and showed accelerated tumor initiation and rapid HCC progression. Early stage HCC tumors (2–3 mm in diameter) were observed in male mice at the age of 47 days and in female mice at the age of 60 days. • Approximately 3 months later, the HCC tumors had progressed to a late stage (> 1 cm in diameter), and 100% of the male and female mice had HCC.