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以Survivin为靶标的肿瘤治疗策略
引用本文:殷海森,赵新颖,苏长.以Survivin为靶标的肿瘤治疗策略[J].第二军医大学学报,2016,37(3):342-348.
作者姓名:殷海森  赵新颖  苏长
作者单位:1. 福建医科大学附属第一医院,福州,350005;2. 第二军医大学东方肝胆外科医院分子肿瘤实验室,上海,200438;3. 福建医科大学附属第一医院,福州350005;第二军医大学东方肝胆外科医院分子肿瘤实验室,上海200438
摘    要:Survivin是凋亡抑制蛋白(inhibitor of apoptosis protein,IAP)家族的新成员,参与调控细胞重要的生理病理过程,具有抑制细胞凋亡、促进细胞增殖和肿瘤间质血管形成等作用.Survivin在正常终末分化组织中几乎检测不到,而在大多数肿瘤组织中高表达,其异常高表达与肿瘤的化疗耐药、肿瘤复发以及患者生存率密切相关.由于在肿瘤发生和发展中起重要作用,Survivin成为肿瘤基因诊治的理想靶点.本文将就Survivin分子功能、Survivin与肿瘤的关系以及与Survivin相关的肿瘤治疗策略作一综述.

关 键 词:survivin  启动子  肿瘤  细胞凋亡  自噬  靶向治疗
收稿时间:9/8/2015 12:00:00 AM
修稿时间:2015/12/15 0:00:00

Survivin-targeted tumor treatment strategy
YIN Hai-sen,ZHAO Xin-ying and SU Chang-qing.Survivin-targeted tumor treatment strategy[J].Academic Journal of Second Military Medical University,2016,37(3):342-348.
Authors:YIN Hai-sen  ZHAO Xin-ying and SU Chang-qing
Institution:Department of Molecular Oncology,Eastern Hepatobiliary Surgery Hospital,Second Military Medical University;The Affiliated First Hospital of Fujian Medical University,The Affiliated First Hospital of Fujian Medical University,Department of Molecular Oncology,Eastern Hepatobiliary Surgery Hospital,Second Military Medical University
Abstract:Survivin, the new member of inhibitors of apoptosis (IAP) family, regulates the essential cellular processes, including inhibiting cell apoptosis, promoting cell proliferation and tumor stromal angiogenesis. Survivin is undetectable in most terminally differentiated tissues, but upregulated in almost all types of human malignancies and its aberrant overexpression positively correlates with chemotherapy resistance, increased tumor recurrence and shortened patient survival. Because of its key role in tumor formation and development, survivin is considered as an ideal target for anticancer treatment. This review will discuss the molecular function of survivin, relationship between survivin and cancer biological characteristics, as well as the research progress of cancer therapy targeting survivin.
Keywords:survivin  cancer  apoptosis  autophagy  targeted therapy
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