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de novo CARCINOGENIC PANCREATIC CANCER CELL STRAIN

机译:从头开始致癌胰腺癌细胞株

摘要

PROBLEM TO BE SOLVED: To provide a pair of a pancreatic cancer model mouse having rapid oncogenicity and cancer cell proliferation potency and a model mouse serving as suitable control for the same, and to simultaneously establish a pancreatic cancer cell strain carcinogenic de novo and a suitable control strain for the same.;SOLUTION: A mating method utilizing a Cre system is used to prepare (a) a human pancreatic cancer model mouse holding "KrasG12D" and "tsA58Tag" and having rapid oncogenicity and (b) its control model mouse not holding the "KrasG12D" but holding only the "tsA58Tag", which are born from the same parents formed of a mouse having the "KrasG12D" and "tsA58Tag" and a mouse holding a Cre gene, and a "rapidly oncogenic pancreatic cancer model cell strain" and a "pancreatic ductal epithelial cell strain" serving as control are established from cells recovered from the mouse pancreas. It is further confirmed that a rapidly oncogenic pancreatic cancer model non-human animal pair can be created by transplanting each of these cell strains. The rapidly oncogenic human pancreatic cancer model mouse pair, the pancreatic cancer model non-human animal pair, and the "rapidly oncogenic pancreatic cancer model cell strain" pair are all excellent as human pancreatic cancer specific analysis tools and effective as a screening system of candidate substances of human pancreatic cancer specific anticancer agents.;COPYRIGHT: (C)2014,JPO&INPIT
机译:解决的问题:提供一对具有快速致癌性和癌细胞增殖潜能的胰腺癌模型小鼠和作为其合适对照的模型小鼠,并同时建立胰腺癌细胞株从头致癌和合适解决方案:采用Cre系统的交配方法用于制备(a)持有“ Kras G12D ”和“ tsA58Tag”并具有快速致癌性的人胰腺癌模型小鼠, (b)其控制模型鼠标不带有“ Kras G12D ”,而仅带有“ tsA58Tag”,它们是由具有“ Kras G12D”的鼠标形成的同一个亲本出生的。从小鼠胰腺中回收的细胞建立起具有Sup>和“ tsA58Tag”的小鼠以及具有Cre基因的小鼠,以及作为对照的“快速致癌胰腺癌模型细胞株”和“胰导管上皮细胞株”。进一步证实,可以通过移植这些细胞株中的每一个来产生快速致癌的胰腺癌模型非人类动物对。快速致癌的人类胰腺癌模型小鼠对,胰腺癌模型非人类动物对和“快速致癌的胰腺癌模型细胞株”对作为人类胰腺癌特异性分析工具均非常出色,并且可以作为候选筛选系统有效胰腺癌特异性抗癌药的化学物质;版权所有:(C)2014,日本专利商标局&INPIT

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