Lung cancer is the leading cause of cancer-related death in the United States despite recent advances in our understanding of this challenging disease. An animal model for high-throughput screening of therapeutic agents for advanced lung cancer could help promote the development of more successful treatment interventions. To develop our orthotopic lung cancer model, luciferase-expressing A549 cancer cells were injected into the mediastinum of athymic nude mice. To determine whether the model would allow easy monitoring of response to therapeutic interventions, tumors were treated with 30 mg/kg Paclitaxel or were irradiated with 5 fractions of 2 Gy, and tumor burden was monitored using bioluminescence imaging. Evidence of radiation-induced lung injury was assessed using immunohistochemical staining for phospho-Smad2/3 and cleaved caspase-3. We found that tumor implantation recapitulated advanced human lung cancer as evidenced by tumor establishment and proliferation within the mediastinum. The tumor responded to Paclitaxel or radiation as shown by decreased tumor bioluminescence and improved overall survival. Immunohistochemistry revealed increased phospho-Smad2/3 and cleaved caspase-3 in irradiated lungs, consistent with radiation-induced lung injury. This orthotopic lung cancer model may help provide a method to assess therapeutic interventions in a preclinical setting that recapitulates locally advanced lung cancer.
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1 October 2011
Research Article|
June 10 2011
A Novel Bioluminescence Orthotopic Mouse Model for Advanced Lung Cancer
Bo Li;
Bo Li
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Artour Torossian;
Artour Torossian
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Wenyan Li;
Wenyan Li
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Stephen Schleicher;
Stephen Schleicher
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Kathy Niu;
Kathy Niu
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Nicholas J. Giacalone;
Nicholas J. Giacalone
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Sung June Kim;
Sung June Kim
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Heidi Chen;
Heidi Chen
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Adriana Gonzalez;
Adriana Gonzalez
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Luigi Moretti;
Luigi Moretti
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
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Bo Lu
Bo Lu
1
Department of Radiation Oncology, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
1 Current address and address for correspondence: Department of Radiation Oncology, Thomas Jefferson University & Hospitals, G-301 Bodine Cancer Center, 111 S. 11th St., Philadelphia, PA 19107; e-mail: bo.lu@jefferson.edu.
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Radiat Res (2011) 176 (4): 486–493.
Article history
Received:
January 12 2011
Accepted:
April 20 2011
Citation
Bo Li, Artour Torossian, Wenyan Li, Stephen Schleicher, Kathy Niu, Nicholas J. Giacalone, Sung June Kim, Heidi Chen, Adriana Gonzalez, Luigi Moretti, Bo Lu; A Novel Bioluminescence Orthotopic Mouse Model for Advanced Lung Cancer. Radiat Res 1 October 2011; 176 (4): 486–493. doi: https://doi.org/10.1667/RR2565.1
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