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作 者:陶海[1] 郭卫春[1] Tao Hai;Guo Weichun(Department of Orthopaedics,Renmin Hospital of Wuhan University,Wuhan 430060)
机构地区:[1]武汉大学人民医院骨科,430060
出 处:《卒中与神经疾病》2020年第1期19-23,共5页Stroke and Nervous Diseases
基 金:国家自然科学基金(81341078)。
摘 要:目的探讨2-甲氧基雌二醇(2-ME)对神经胶质瘤U251细胞移植瘤的增殖抑制、凋亡及可能的分子机制。方法构建胶质瘤裸鼠移植瘤模型,经2-ME治疗后分别记录移植瘤的重量、体积;通过移植瘤HE、免疫组化、TUNEL染色分析2-ME对移植瘤的增殖抑制、凋亡及对Bcl-2、VEGF表达水平的影响;检测2-ME对裸鼠肝肾功能的影响。结果 2-ME对肿瘤的体积和重量均有抑制作用;HE染色显示实验组出现不同程度的肿瘤细胞密度减低;免疫组化染色显示,随着2-ME水平的升高,肿瘤组织内Bcl-2、VEGF的表达水平逐渐下降;TUNEL染色显示2-ME诱导裸鼠移植瘤组织细胞凋亡;肝肾功能检测未见损害发生。结论 2-ME在体内能有效抑制胶质瘤移植瘤的生长、诱导其凋亡,其抗肿瘤作用可能与Bcl-2、VEGF表达水平有关,且无明显毒副作用。Objective To investigate the proliferation inhibition, apoptosis and possible molecular mechanism of 2-methoxyestradiol(2-ME) on glioma xenograft tumor. Methods The xenograft model of glioma in nude mice was constructed in vivo. After treatment with 2-ME, the weight and volume of the xenograft tumor were recorded. The effects of 2-ME on proliferation inhibition, apoptosis and expression of Bcl-2 and VEGF in xenograft tumors were analyzed by HE, immunohistochemistry and TUNEL staining experiments. Liver and kidney function test in nude mice. Results 2-ME inhibited the volume and weight of tumors;HE staining showed that the experimental group showed different degrees of tumor cell density reduction,the results of immunohistochemistry showed that the expression of Bcl-2 and VEGF decreased gradually with the increase of 2-ME concentration. TUNEL staining showed that 2-ME induced apoptosis of xenograft tumor cells in nude mice,no damage occurred in liver and kidney function tests. Conclusion 2-ME could effectively inhibit the proliferation and induced apoptosis of glioma xenografts, and its anti-tumor effect might be related to Bcl-2 and VEGF, and no obvious side effects.
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