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PMID: 18344688 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

The let-7 microRNA reduces tumor growth in mouse models of lung cancer.

Cell cycle (Georgetown, Tex.) ·Vol. 7 ·No. 6 ·2008-03-15 ·Pages 759-64

Esquela-Kerscher A, Trang P, Wiggins JF, Patrawala L, Cheng A, Ford L, Weidhaas JB, Brown D, Bader AG, Slack FJ

Abstract

MicroRNAs have been increasingly implicated in human cancer and interest has grown about the potential to use microRNAs to combat cancer. Lung cancer is the most prevalent form of cancer worldwide and lacks effective therapies. Here we have used both in vitro and in vivo approaches to show that the let-7 microRNA directly represses cancer growth in the lung. We find that let-7 inhibits the growth of multiple human lung cancer cell lines in culture, as well as the growth of lung cancer cell xenografts in immunodeficient mice. Using an established orthotopic mouse lung cancer model, we show that intranasal let-7 administration reduces tumor formation in vivo in the lungs of animals expressing a G12D activating mutation for the K-ras oncogene. These findings provide direct evidence that let-7 acts as a tumor suppressor gene in the lung and indicate that this miRNA may be useful as a novel therapeutic agent in lung cancer.

MeSH Terms
Adenoviridae Administration, Intranasal Animals Cell Line, Tumor Cell Proliferation Genes, Tumor Suppressor Genetic Therapy/methods Genetic Vectors Humans Lung Neoplasms/genetics,therapy Mice MicroRNAs/administration & dosage,therapeutic use
Chemicals
MicroRNAs mirnlet7 microRNA, human
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Esquela-Kerscher Aurora
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA.
Trang Phong
Wiggins Jason F
Patrawala Lubna
Cheng Angie
Ford Lance
Weidhaas Joanne B
Brown David
Bader Andreas G
Slack Frank J
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1551-4005
Published
2008-03-15
Epub
2008-00-03
Pages
759-64
Language
English
Region
United States
NLM ID
101137841
Subset
IM
Grants
NIGMS NIH HHS · F32 GM071157 · United States
NCI NIH HHS · F32CA130376 · United States
NIGMS NIH HHS · F32GM071157 · United States
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