首页> 外国专利> Method for screening anti-cancer material using mutant ?53 protein having gain-of-function which is a target protein as a mediator related to the suppression of cancer

Method for screening anti-cancer material using mutant ?53 protein having gain-of-function which is a target protein as a mediator related to the suppression of cancer

机译:使用具有作为目标蛋白的功能增强的突变型β53蛋白作为与癌症抑制有关的介质来筛选抗癌物质的方法

摘要

Mutant p53 protein of the invention is a target protein as a cancer-related inhibitory agent. Mutant p53 proteins of the present invention has a function to suppress the induced cell death as a function acquiring sex mutant protein, a STAT3 protein expression induction or activation of the STAT3 protein. Specifically, the mutant p53 protein of the present invention inhibit the cell death through activation STAT3 protein. With the mutant p53 protein of the present invention can develop effective cancer therapy or cancer therapy. According to the invention, wherein for cancer-cell mutant p53 protein having apoptotic function anticancer candidate key target protein as a utilization point complex, yet comprehensive action more than STAT3 using controlled in the previous stage high STAT3 expression and activity of a substance It may screen for an antitumor substance and to analyze its performance. ; Anaplastic thyroid cancer, p53 mutations, mutation function acquired gender, Miss sense mutations, glycine, valine, apoptosis inhibition, the target protein, the cancer therapeutic screening, STAT3 activation
机译:本发明的突变体p53蛋白是作为与癌症相关的抑制剂的靶蛋白。本发明的突变体p53蛋白具有获得性突变蛋白,STAT3蛋白表达诱导或STAT3蛋白激活的功能,具有抑制诱导的细胞死亡的功能。具体地,本发明的突变体p53蛋白通过激活STAT3蛋白来抑制细胞死亡。用本发明的突变体p53蛋白可以开发有效的癌症疗法或癌症疗法。根据本发明,其中对于具有凋亡功能的抗癌候选关键靶蛋白作为癌细胞利用点复合物的癌细胞突变体p53蛋白,在前一阶段通过控制STAT3的高表达和活性,可以发挥比STAT3更全面的作用。抗肿瘤物质并分析其性能。 ;间变性甲状腺癌,p53突变,获得性别的突变功能,有义突变,甘氨酸,缬氨酸,凋亡抑制,靶蛋白,癌症治疗筛选,STAT3激活

著录项

  • 公开/公告号KR101038570B1

    专利类型

  • 公开/公告日2011-06-02

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20080109816

  • 发明设计人 김태현;유영현;이상률;

    申请日2008-11-06

  • 分类号C07K14/00;C12N15/09;

  • 国家 KR

  • 入库时间 2022-08-21 17:50:12

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