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国家自然科学基金(30671958)

作品数:2 被引量:4H指数:1
相关作者:赵帆于继云崔健张纪岩更多>>
相关机构:军事医学科学院更多>>
发文基金:国家自然科学基金更多>>
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靶向肿瘤血管的抗体免疫治疗
2008年
肿瘤细胞引起多样性和易突变性很难直接用药物治疗,并且肿瘤细胞的耐药性也已成为治疗的一个瓶颈。靶向肿瘤血管的抗体治疗通过靶向实体肿瘤内血管内皮细胞生长增殖的相关靶点,切断肿瘤细胞的营养供应从而达到治疗肿瘤的目的。本文中总结了近年来世界各国已上市或处于临床阶段及实验室阶段的靶向肿瘤血管抗体药物,并阐述了该治疗策略的特点及部分抗体药物的作用机制,提出目前存在的问题和相关解决方法,为靶向肿瘤血管的抗体治疗研究提供一定的参考。
崔健赵帆张纪岩于继云
关键词:抗体药物免疫治疗
cAMP Modulates Macrophage Development by Suppressing M-CSF-Induced MAPKs Activation被引量:4
2008年
M-CSF is a key cytokine in macrophage development by inducing MAPKs activation, and cAMP can inhibit MAPKs activation induced by inflammatory stimuli. To explore the effects of cAMP on M-CSF-induced MAPKs activation and on macrophage development, the model of bone marrow-derived murine macrophages (BMMs) was used. The effects of cAMP on M-CSF-induced MAPKs activation were analyzed by Western blotting assay, and the effects of cAMP on CD14 and F4/80 expression during macrophage development were examined by FACS analysis. Macrophage morphology showed the successful establishment of the model of macrophage development. Western blotting assay revealed that M-CSF activated ERK, JNK and p38 in both mature and immature macrophages, and cAMP inhibited M-CSF-induced ERK, JNK and p38 activation in a time-dependent manner. FACS analysis revealed that macrophage development was impaired with cAMP pretreatment. In conclusion, cAMP modulates macrophage development by suppressing M-CSF-induced MAPKs activation. Cellular & Molecular Immunology.
Ning ZhuJian CuiChunxia QiaoYan LiYuanfang MaJiyan ZhangBeifen Shen
关键词:M-CSF
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