检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]昆明理工大学生命科学与技术学院,昆明650500
出 处:《中国细胞生物学学报》2016年第7期864-872,共9页Chinese Journal of Cell Biology
基 金:国家自然科学基金(批准号:81260351;81360162)资助的课题~~
摘 要:肿瘤坏死因子相关凋亡诱导配体(tumor necrosis factor related apoptosis inducing ligand,TRAIL)只有与细胞膜上死亡受体结合才能促使癌细胞凋亡,一旦细胞膜上的死亡受体发生缺失或失去活性,将使癌细胞对TRAIL极为耐受。近年来,对死亡受体的研究发现,死亡受体异常表达可能是死亡受体在细胞膜上发生功能性缺失的最主要原因。该文主要探究肿瘤细胞中死亡受体在转录调控、翻译后修饰、转运和内化过程中的异常情况,期望为今后研发克服TRAIL耐受的联合药物及癌症治疗提供参考。Tumor necrosis factor related apoptosis inducing ligand (TRAIL) can induce tumor apoptosis only after binding to its cognate death receptors (DRs) on the plasma membrane. The loss of DRs on the surface of cancer cells will result in tumor resistance to TRAIL-induced apoptosis and cell death. Recent studies have demonstrated that abnormal expression of death receptors may be the primary cause of the loss of cell surface death receptors. This review highlights the abnormal situation of death receptors in tumor cells, including the regulatory roles of transcription, post-translation modifications, trafficking and internalization, are possible mechanisms for the loss of death receptors in cell surface. This review provides a further reference theoretical basis for the development of multiple drugs combination therapy to overcome TRAIL resistance and to improve cancer therapy.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.28