Bone metastasis of lung cancer in a mouse model with normal immune function / 南方医科大学学报
Journal of Southern Medical University
;
(12): 664-668, 2014.
Artigo
em Chinês
| WPRIM
| ID: wpr-249385
ABSTRACT
<p><b>OBJECTIVE</b>To establish a model bearing human lung cancer xenograft with bone metastasis in mice with normal immune function.</p><p><b>METHODS</b>Forty female C57BL/6J mice were randomly allocated into 4 equal groups, including a control group and 3 immunosuppression groups treated with low, moderate, and high doses of dexamethasone (50, 100, and 150 mg, respectively). Four days after immune suppression, the mice were subjected to percutaneous injection of1.0×10(9) L(-1) A549 cells into the tibial plateau, and the bone defects were assessed radiographically 28 days after modeling. HE staining and immunohistochemical staining were used to examine the tumor tissues and bone tissue damages.</p><p><b>RESULTS</b>In each of the 4 groups one mouse died during tumor cell injection. Only 1 mouse showed tumor formation in low-dose immunosuppression group, as compared to 7 and 4 in moderate- and high-dose immunosuppression groups. X-ray and microCT scan showed significant tibial bone destruction in moderate- and high-dose groups. The moderate- and high-dose groups showed similar ALP activities but both were significantly higher than those in the other two groups (P<0.05).</p><p><b>CONCLUSION</b>Immunosuppression with a moderate dose of dexamethasone results in longer survival time of the human lung cancer xenograft-bearing model mice as well as a higher tumor formation rate.</p>
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Patologia
/
Farmacologia
/
Neoplasias Ósseas
/
Dexametasona
/
Terapia de Imunossupressão
/
Linhagem Celular Tumoral
/
Modelos Animais de Doenças
/
Neoplasias Pulmonares
/
Camundongos Endogâmicos C57BL
/
Transplante de Neoplasias
Limite:
Animais
/
Feminino
/
Humanos
Idioma:
Chinês
Revista:
Journal of Southern Medical University
Ano de publicação:
2014
Tipo de documento:
Artigo
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