项目名称: miR-29b/STAT3/GATA3正反馈环路逆转TAM极化并抑制尤文肉瘤恶性表型的机制研究
项目编号: No.81502329
项目类型: 青年科学基金项目
立项/批准年度: 2016
项目学科: 医药、卫生
项目作者: 张中卒
作者单位: 重庆医科大学
项目金额: 18万元
中文摘要: 尤文肉瘤(ES)是高度恶性的原发骨肿瘤,肿瘤相关巨噬细胞(TAM)在局部微环境中的浸润与肿瘤转移和复发相关,因此改善微环境中TAM浸润是治愈ES的关键。课题小组以转移与TAM浸润的相关性为切入点,发现并验证miR-29b与尤文肉瘤TAM浸润密切相关,而参与M2型极化作用的STAT3是miR-29b的靶基因之一,后者能够通过抑制GATA3表达进一步反馈抑制miR-29b的转录,我们推测miR-29b/STAT3/GATA3环路能够逆转尤文肉瘤TAM极化并抑制ES恶性生物学表型。研究拟以miR-29b为研究对象,分别在ES细胞系及荷瘤裸鼠中考察miR-29b对TAM介导的尤文肉瘤恶性生物学表型的影响;另一方面通过研究miR-29b对体外单核细胞极化及其分泌细胞因子的作用,检测其对TAM极化及表型的影响,并验证miR-29b/STAT3/GATA3通路在该作用中的调控机制。
中文关键词: 尤文肉瘤;肿瘤相关巨噬细胞;MiR-29b;信号通路;分子机制
英文摘要: Ewing sarcoma (ES) is a kind of primary bone tumor with great malignancy. Multiple tumor-associated macrophages (TAM) were reported to negatively related with tumor metastasis and recurrence. Thus, it is suggested to be a new way for ES therapy in the future. Considered the relationship between metastasis and TAM infiltration as the breakthrough point, we found and identified that miR-29b expression was closely related with the infiltration of TAM in the ES tissues. Interestingly, STAT3, which played a critical role in the regulation of macrophage polarization, was predicted to be a putative target gene of miR-29b. Moreover, through suppressing the expression of GATA3, overexpression of STAT3 suppressed the expression of miR-29b, which makes us to speculate that the feedback loop of miR-29b/STAT3/GATA3 might play an important role in the regulation of macrophage polarization and its-associated suppression on the malignant phenotype of ES. In this paper, we will further explore the effects of miR-29b on TAM-associated suppression on the malignant phenotype of ES, and further identify its influence on the macrophage polarization in ES cells and mice. Lastly, we will further verify whether miR-29b/STAT3/GATA3 loop was involved in the effects.
英文关键词: Ewing's sarcoma;Tumor associated macrophages;MiR-29b;Signal pathway;Molecular mechanism