Mouse model for lung tumorigenesis through Cre/lox controlled sporadic activation of the K-Ras oncogene.

Abstract:

:The onset of human lung cancer occurs through sequential mutations in oncogenes and tumor suppressor genes. Mutations in K-Ras play a prominent role in human non-small cell lung cancer. We have developed a mouse lung tumor model in which K-Ras can be sporadically activated through Cre-lox mediated somatic recombination. Adenoviral mediated delivery of Cre recombinase in lung epithelial cells gave rise to rapid onset of tumorigenesis, yielding pulmonary adenocarcinomas with 100% incidence after a short latency. The lung tumor lesions shared many features with human non-small cell lung cancer. Our data show that sporadic expression of the K-Ras oncogene is sufficient to elicit lung tumorigenesis. Therefore this model has many advantages over conventional transgenic models used thus far.

journal_name

Oncogene

journal_title

Oncogene

authors

Meuwissen R,Linn SC,van der Valk M,Mooi WJ,Berns A

doi

10.1038/sj.onc.1204837

subject

Has Abstract

pub_date

2001-10-04 00:00:00

pages

6551-8

issue

45

eissn

0950-9232

issn

1476-5594

journal_volume

20

pub_type

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