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PMID: 11751630 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras.

Genes & development ·Vol. 15 ·No. 24 ·2001-12-15 ·Pages 3243-8

Jackson EL, Willis N, Mercer K, Bronson RT, Crowley D, Montoya R, Jacks T, Tuveson DA

Abstract

Adenocarcinoma of the lung is the most common form of lung cancer, but the cell of origin and the stages of progression of this tumor type are not well understood. We have developed a new model of lung adenocarcinoma in mice harboring a conditionally activatable allele of oncogenic K-ras. Here we show that the use of a recombinant adenovirus expressing Cre recombinase (AdenoCre) to induce K-ras G12D expression in the lungs of mice allows control of the timing and multiplicity of tumor initiation. Through the ability to synchronize tumor initiation in these mice, we have been able to characterize the stages of tumor progression. Of particular significance, this system has led to the identification of a new cell type contributing to the development of pulmonary adenocarcinoma.

MeSH Terms
Adenocarcinoma/genetics,metabolism,pathology Animals Codon Disease Progression Gene Expression Genes, ras/genetics Immunoenzyme Techniques Integrases/metabolism Lung Neoplasms/genetics,metabolism,pathology Mice Mice, Knockout Models, Animal Mutation Proto-Oncogene Proteins p21(ras)/metabolism Time Factors Viral Proteins/metabolism
Chemicals
Codon Viral Proteins Cre recombinase Integrases Proto-Oncogene Proteins p21(ras)
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Jackson E L
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Willis N
Mercer K
Bronson R T
Crowley D
Montoya R
Jacks T
Tuveson D A
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Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
2001-12-15
Pages
3243-8
Language
English
Region
United States
NLM ID
8711660
PMCID
PMC312845
Subset
IM
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