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The Predictive Value of Vascular Endothelial Growth Factor and Nm23 for the Diagnosis of Occult Metastasis in Non‐small Cell Lung Cancer

We assessed the association of vascular endothelial growth factor (VEGF) and nml23 expression with occult micrometastasis in lung cancer. As destination sites for micrometastasis, we scrutinized lymph node (LN) and bone marrow (BM) specimens. For LN, 122 stage I patients who had received curative op...

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Detalles Bibliográficos
Autores principales: Ohta, Yasuhiko, Nozaki, Zensei, Nozawa, Hiroshi, Kamesui, Tadashi, Tsunezuka, Yoshio, Oda, Makoto, Watanabe, Go
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926704/
https://www.ncbi.nlm.nih.gov/pubmed/11267948
http://dx.doi.org/10.1111/j.1349-7006.2001.tb01103.x
Descripción
Sumario:We assessed the association of vascular endothelial growth factor (VEGF) and nml23 expression with occult micrometastasis in lung cancer. As destination sites for micrometastasis, we scrutinized lymph node (LN) and bone marrow (BM) specimens. For LN, 122 stage I patients who had received curative operations were studied. As regards BM, 203 patients in stage I‐IV who underwent operations were registered. Immunohistochemical anti‐cytokeratin staining was used to detect microdissemination of cancer cells. The VEGF and the nm23 expression at the primary sites were immunohistochemically studied in 285 cases in total. The percentages of the patients with micro‐dissemination were 28.7% for LN and 42.4% for BM. The outcome for the patients with LN or BM microdissemination was significantly worse than that for patients without it. The increased VEGF and the decreased nm23 expression within primary tumors were significantly associated with LN and BM microdissemination. The results indicate possible value of using these biological markers to predict the risk of systemic micrometastasis in non‐small cell lung cancer.