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Establishment and Characterization of Immortalized Miniature Pig Pancreatic Cell Lines Expressing Oncogenic K-Ras(G12D)

In recent decades, many studies on the treatment and prevention of pancreatic cancer have been conducted. However, pancreatic cancer remains incurable, with a high mortality rate. Although mouse models have been widely used for preclinical pancreatic cancer research, these models have many differenc...

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Detalles Bibliográficos
Autores principales: Yang, Hae-Jun, Song, Bong-Seok, Sim, Bo-Woong, Jung, Yena, Chae, Unbin, Lee, Dong Gil, Cha, Jae-Jin, Baek, Seo-Jong, Lim, Kyung Seob, Choi, Won Seok, Lee, Hwal-Yong, Son, Hee-Chang, Park, Sung-Hyun, Jeong, Kang-Jin, Kang, Philyong, Baek, Seung Ho, Koo, Bon-Sang, Kim, Han-Na, Jin, Yeung Bae, Park, Young-Ho, Choo, Young-Kug, Kim, Sun-Uk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700231/
https://www.ncbi.nlm.nih.gov/pubmed/33233448
http://dx.doi.org/10.3390/ijms21228820
Descripción
Sumario:In recent decades, many studies on the treatment and prevention of pancreatic cancer have been conducted. However, pancreatic cancer remains incurable, with a high mortality rate. Although mouse models have been widely used for preclinical pancreatic cancer research, these models have many differences from humans. Therefore, large animals may be more useful for the investigation of pancreatic cancer. Pigs have recently emerged as a new model of pancreatic cancer due to their similarities to humans, but no pig pancreatic cancer cell lines have been established for use in drug screening or analysis of tumor biology. Here, we established and characterized an immortalized miniature pig pancreatic cell line derived from primary pancreatic cells and pancreatic cancer-like cells expressing K-ras(G12D) regulated by the human PTF1A promoter. Using this immortalized cell line, we analyzed the gene expression and phenotypes associated with cancer cell characteristics. Notably, we found that acinar-to-ductal transition was caused by K-ras(G12D) in the cell line constructed from acinar cells. This may constitute a good research model for the analysis of acinar-to-ductal metaplasia in human pancreatic cancer.