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Gut:BTK激酶与食管癌

2017-08-24 zhangfan MedSci原创

研究认为BTK激酶是有效的抗食道癌靶点,目前ibrutinib治疗MYC 和(或) ERBB2过表达的中晚期食管癌的II期临床研究正在进行中

食管癌是全球癌症相关死亡的第七大因素,该疾病复发频繁且治疗选择有限。近日研究人员对食管癌相关生物标志物进行了研究。研究人员将17个食管癌细胞系的基因组图谱与小分子抑制剂药物敏感性数据相结合,确定与癌症驱动基因相关的药物敏感效应。研究同时考察了肿瘤细胞系RNA干扰数据,以确定候选基因依赖性或可作为治疗靶点的可能性。研究发现BTK 激酶具有潜在的食道癌治疗效果,BTK/ERBB2激酶抑制剂ibrutinib可显著抑制食道癌模型的疾病进展,在MYC以及ERBB2过表达细胞系中,ibrutinib 可以降低ERK介导的信号转导,抑制cMYC磷酸化,减低MYC蛋白水平,引起G1细胞周期阻滞和凋亡。研究认为BTK激酶是有效的抗食道癌靶点,目前ibrutinib治疗MYC 和(或) ERBB2过表达的中晚期食管癌的II期临床研究正在进行中。原始出处:Irene Yushing Chong et al. Mapping genetic vulnerabilities reveals BTK as a novel therapeutic target in oesophageal cancer . Gu

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    2017-09-07 1771ae4158m

    学习一下很不错

    0

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    2017-08-26 zhouqu_8
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    2017-08-26 redcrab
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    2017-08-26 fengting7
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objectType=article, channel=null, level=null, likeNumber=42, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/NUyjXTCJjo7cJ6ejWUr2nIia8qOvAKNdLHr32Df6G8iaoaOx6pHaoiacwp26DaslxZHCGbibZhhCGven4rvmWP60GahtzgFjgCjR/0, createdBy=6b111703011, createdName=有备才能无患, createdTime=Thu Aug 24 23:06:14 CST 2017, time=2017-08-24, status=1, ipAttribution=)]
    2017-08-25 刘煜

    学习了谢谢分享

    0

  6. 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    2017-08-25 明月清辉

    谢谢分享.学习了

    0

  7. 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    2017-08-25 龙胆草

    学习谢谢分享

    0

  8. 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    2017-08-25 yfjms

    学习了

    0

  9. 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    2017-08-25 luominglian113

    学习了.谢谢分享

    0

  10. 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    2017-08-24 有备才能无患

    研究认为BTK激酶是有效的抗食道癌靶点.目前ibrutinib治疗MYC和(或)ERBB2过表达的中晚期食管癌的II期临床研究正在进行中.

    0

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近日,来自莱斯特大学和莱斯特医院的研究人员通过研究共同宣布了一项重大的科研进展,研究人员对急性期间病人进行临床试验发现,一种特殊新药可以帮助治疗化疗耐受的慢性淋巴细胞性白血病和非霍奇金淋巴瘤,相关研究刊登于国际著名杂志Blood上。这是该药的首个人体研究。研究人员观察了新型抑制剂药物ONO/GS-4059在治疗对当前化疗耐受的慢性淋巴细胞性白血病和非霍奇金淋巴瘤患者中的反应。药物ONO/GS-40

PNAS:酶BTK在抗病毒感染中发挥关键作用

身体对入侵的细菌或病毒产生的初始反应是由先天免疫系统调控着的,在这种免疫系统中,细胞分泌出被称作细胞因子的信号分子从而促进炎症产生和对被身体识别为外来物质的靶标发动一般性反击。比如,蛋白Toll样受体3(Toll-like receptor 3, TLR3)有助于启动对抗病毒的先天免疫反应。 如今,来自新加坡科技研究局(A*STAR)下属的生物处理科技研究院的Kong-Peng Lam和同事们证

Clin Cancer Res:Ibrutinib治疗能抑制BTK和VLA-4依赖粘附的慢性淋巴细胞白血病

目的:Ibrutinib导致慢性淋巴细胞白血病(CLL)患者瞬态淋巴球增多,这发生于药物开始的几小时内,是因为从淋巴组织进入血液中有细胞流出。因此,我们试图探讨ibrutinib对体内慢性淋巴细胞白血病细胞迁移和粘附的影响。实验设计:在研究-起始的II期试验阶段,患者接受单一剂量ibrutinib(420毫克每天)。收集预处理的和治疗期间来自体内的功能分析的连续血液样本。结果:慢性淋巴细胞白血病细

Arthritis Rheumatol:自身免疫性疾病患者外周血B淋巴细胞Bruton酪氨酸激酶活性增强

这些数据表明人类自身免疫性疾病的特征在于BTK活性增强,BTK活性增强不仅与自身抗体形成并且与T细胞活性有关。

Sci Rep:中科院刘青松教授研发出治疗类风湿性关节炎的BTK抑制剂

近日,国际学术权威刊物自然出版集团旗下子刊《Scientific Reports》杂志在线发表了中国科学院合肥物质科学研究院强磁场科学中心研究员刘青松、刘静课题组与安徽医科大学教授魏伟课题组合作发展了一种新型的针对治疗类风湿性关节炎的BTK激酶抑制剂CHMFL-BTK-11。研究题为Irreversible inhibition of BTK kinase by a novel highly se

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