摘要
恶性胸腔积液(malignantpleuraleffusion.MPE)是恶性肿瘤晚期并发症之一。最新研究表明血管内皮生长因子(VEGF)是恶性胸水形成的关键介质。Yeh等对人肺腺癌及动物模型研究发现,恶性胸水的产生受到VEGF的调节,同时也观察到激活的Stat3(信号传导子及转录激活子蛋白)上调VEGF的表达。证实恶性胸水中存在持续激活的Stat3、高表达的IL-6和VEGF。因此他们假设自分泌IL-6激活Stat3,进而上调VEGF表达.参与恶性胸水的形成。本文就恶性胸水的诊断和治疗进展作一简要介绍:
出处
《现代医药卫生》
2009年第18期2816-2818,共3页
Journal of Modern Medicine & Health
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共引文献43
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