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A mouse model for EML4-ALK-positive lung cancer.

EML4-ALK is a fusion-type protein tyrosine kinase that is generated in human non-small-cell lung cancer (NSCLC) as a result of a recurrent chromosome inversion, inv (2)(p21p23). Although mouse 3T3 fibroblasts expressing human EML4-ALK form transformed foci in culture and s.c. tumors in nude mice, it has remained unclear whether this fusion protein plays an essential role in the carcinogenesis of NSCLC. To address this issue, we have now established transgenic mouse lines that express EML4-ALK specifically in lung alveolar epithelial cells. All of the transgenic mice examined developed hundreds of adenocarcinoma nodules in both lungs within a few weeks after birth, confirming the potent oncogenic activity of the fusion kinase. Although such tumors underwent progressive enlargement in control animals, oral administration of a small-molecule inhibitor of the kinase activity of ALK resulted in their rapid disappearance. Similarly, whereas i.v. injection of 3T3 cells expressing EML4-ALK induced lethal respiratory failure in recipient nude mice, administration of the ALK inhibitor effectively cleared the tumor burden and improved the survival of such animals. These data together reinforce the pivotal role of EML4-ALK in the pathogenesis of NSCLC in humans, and they provide experimental support for the treatment of this intractable cancer with ALK inhibitors.

Pubmed ID: 19064915

Authors

  • Soda M
  • Takada S
  • Takeuchi K
  • Choi YL
  • Enomoto M
  • Ueno T
  • Haruta H
  • Hamada T
  • Yamashita Y
  • Ishikawa Y
  • Sugiyama Y
  • Mano H

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

December 16, 2008

Associated Grants

None

Mesh Terms

  • 3T3 Cells
  • Animals
  • Carcinoma, Non-Small-Cell Lung
  • Disease Models, Animal
  • Humans
  • Lung Neoplasms
  • Mice
  • Mice, Transgenic
  • Oncogene Proteins, Fusion
  • Protein Kinase Inhibitors