摘要
目的:研究B F基因及其丝裂原活化蛋白/胞外信号调节激酶的激酶(mitogen-activated protein/extracellular signal-regulated kinase kinase,MEK)/细胞外信号调节激酶(extracellular signal-regulated kinase,ERK)信号通路与甲状腺乳头状癌发生的相关性及部分作用机制。方法:收集73例散发的甲状腺乳头状癌患者及16例同期甲状腺瘤患者(对照组)的临床资料及标本。采用免疫组织化学和免疫印迹法检测两组标本组织中的大鼠肉瘤蛋白(ratsarcoma,S),B F,MEK1/2和ERK1/2表达状况。结果:甲状腺乳头状癌组S,B F,pMEK1/2和pERK1/2表达水平明显高于甲状腺瘤组(P<0.05或P<0.01);甲状腺乳头状癌患者S,B F,pMEK1/2和pERK1/2表达与肿块大小、淋巴结转移以及临床分期相关(P<0.05或P<0.01)。结论:S,B F,pMEK1/2及pERK1/2可能与甲状腺乳头状癌发生及其淋巴结转移、临床分期相关;B F可能通过激活MEK/ERK信号通路而发挥其生物作用。
To determine the association between activity of BRAF and mitogen-activated protein/ extracellular signal-regulated kinase kinase (MEK) / extracellular signal-regulated kinase (ERK) signal pathway in papillary thyroid cancer and its mechanism. Methods: We collected the clinical data and blood samples from 73 cases of papillary thyroid cancer and another 16 cases of benign thyroid gland tumor, and detected the expression of rat sarcoma (RAS), BRAE MEK1/2, and ERK1/2 in all tumor specimens and benign thyroid tissues with immunohistochemistry and Western blot. Results: The expression of RAS, BRAF, pMEK1/2, and pERK1/2 protein in papillary thyroid cancer tissues was higher than those in the benign thyroid tissues(P〈0.05 or P〈0.01). The expression of RAS, BRAF, MEK1/2, and ERK1/2 was associated withthe tumor size, the lymph node metastasis, and the clinical stage of papillary thyroid cancer(P〈0.05 or P〈0.01). Conclusion: The expression of RAS, BRAF, pMEK1/2, and pERK1/2 is associated with the pathogenesis, the lymph node metastasis, and the clinical stage of papillary thyroid cancer. The MEK/ERK signaling pathway may be activated by BRAF in papillary thyroid cancer.
出处
《中南大学学报(医学版)》
CAS
CSCD
北大核心
2012年第9期889-894,共6页
Journal of Central South University :Medical Science
基金
湖南省发展与改革委员会资助项目(2009-1390)~~