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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

机译:血管内皮生长因子和Nm23对非小细胞肺癌隐匿性转移诊断的预测价值

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摘要

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.
机译:我们评估了血管内皮生长因子(VEGF)和nml23表达与肺癌隐匿性微转移的关系。作为微转移的目的地,我们仔细检查了淋巴结(LN)和骨髓(BM)标本。对于LN,研究了122例接受过根治性手术的I期患者。关于BM,登记了I-IV期手术的203例患者。免疫组织化学抗细胞角蛋白染色用于检测癌细胞的微扩散。免疫组织化学研究了285例患者的主要部位的VEGF和nm23表达。 LN和BM的微传播患者百分比分别为28.7%和42.4%。 LN或BM微弥散患者的结局显着差于没有LN或BM微弥散的患者。原发性肿瘤内VEGF的增加和nm23表达的减少与LN和BM的微扩散显着相关。结果表明,使用这些生物标记物预测非小细胞肺癌系统性微转移的风险可能具有价值。

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