摘要
目的探讨脾酪氨酸激酶(Syk)和血管内皮生长因子(VEGF)-C在胰腺癌中的表达变化及其与淋巴转移的关系。方法应用免疫组化技术检测40例胰腺癌组织、正常胰腺组织和慢性胰腺炎组织中Syk和VEGF-C的表达情况。结果慢性胰腺炎、正常胰腺组织均表达Syk,其表达阳性率分别为77.8%、100%;在胰腺癌中多呈中等或弱阳性表达,阳性率为27.5%,显著低于前两者(P〈0.01)。Syk与肿瘤的发生部位、分化程度和淋巴结转移无关,而与TNM分期有关,Ⅰ~Ⅱ期者表达明显高于Ⅲ~Ⅳ期者(P〈0.05)。胰腺癌组织中VEGF—C阳性率为73%(29/40)。VEGF—C表达阳性者,淋巴结转移显著增多(P〈0.05)。VEGF—C与Syk的表达具有显著相关性(P=0.019)。结论Syk在胰腺癌中表达减低或缺失,与胰腺癌的发展显著相关,VEGF-C主要参与胰腺癌淋巴管生成的调控并促讲淋巴转移.在胰腺痛的侵袭和转移讨稗中Svk与VEGF—C且有协同作用.
Objective To investigate the expression of Syk and VEGF-C in pancreatic cancer and relation to lymphatic metastasis. Method The expression of Syk and VEGF-C was assayed by means of immunohistochemistry in 40 pancreatic carcinomas,9 chronic inflammation and 8normal tissues. Results The positive rates of Syk were 27.5% ,77. 8% and 100% ,respectively in pancreatic cancer, chronic inflammation and normal tissues. The expression of Syk in pancreatic cancer was significantly lower than that in other two kinds of tissues ( P 〈 0. 01 ). There was no correlation between Syk expression and the site,differentiation and metastasis. Syk in Ⅰ -Ⅱ stages of pancreatic cancer showed stronger expression than that in Ⅲ-Ⅳ stages. The positive rate of VEGF-C was 73% in pancreatic cancer. The positive lymph node in positive VEGF-C group were higher than that in the negative group (P 〈 0. 05). There was significant correlation between Syk and VEGF-C expression in pancreatic cancer (P = 0. 019). Conclusions The expression of Syk in pancreatic cancer is significantly lower, which is related to development of pancreatic cancer. VEGF-C participats in the regulation of lymphangiogenisis,induces lymphangiogenisis in pancreatic cancer, and promotes the tumor lymphatic metastasis. Syk and VEGF-C have the effect of mutual cooperation in the process of pancreatic cancer.
出处
《山东医药》
CAS
北大核心
2008年第21期29-31,共3页
Shandong Medical Journal
基金
国家自然科学基金资助项目(30571712)
山东省中青年科学家科技奖励基金资助项目(2005BS03003)
山东省医药卫生科研资助项目(2005HW133)
关键词
胰腺肿瘤
脾酪氨酸激酶
血管内皮生长因子
淋巴转移
pancreatic neoplasm
spleen tyrosine kinase
vascular endothelial growth factor
lymphatic metastasis