【摘 要】
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Pancreatic cancer is one of the leading causes of cancer death.KRAS mutation is present in 95% of human pancreatic ductal adenocarcinoma (PDAC).Transgenic mouse models reveal that KRAS signaling is su
【机 构】
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Department of Pathology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences & P
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Pancreatic cancer is one of the leading causes of cancer death.KRAS mutation is present in 95% of human pancreatic ductal adenocarcinoma (PDAC).Transgenic mouse models reveal that KRAS signaling is sufficient to reprogram pancreatic cells into PDAC, but with a long latency.However, both mutations in KRAS and TP53,INK4a or SMAD4 result in a much earlier appearance of highly invasive and metastatic pancreatic cancer.To further investigate the molecular mechanisms of pancreatic cancer metastasis, we applied a genome-wide random mutagenesis strategy in a lowmetastatic mouse pancreatic cancer cell line Pan02,and implemented series of screening of metastatic conversions from low-metastatic to high metastatic potential using an orthotopic mouse model.
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