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MCIR1: A patient-derived mantle cell lymphoma line for discovering new treatments for ibrutinib resistance
European Journal of Haematology ( IF 3.1 ) Pub Date : 2021-07-02 , DOI: 10.1111/ejh.13682 Xiaosheng Wu 1 , Kevin E Nowakowski 1 , Jithma P Abeykoon 1 , Michelle Manske 1 , Mary J Stenson 1 , Michael M Timm 2 , Curtis A Hanson 2 , Daniel L Van Dyke 2 , Surendra Dasari 3 , Thomas E Witzig 1
European Journal of Haematology ( IF 3.1 ) Pub Date : 2021-07-02 , DOI: 10.1111/ejh.13682 Xiaosheng Wu 1 , Kevin E Nowakowski 1 , Jithma P Abeykoon 1 , Michelle Manske 1 , Mary J Stenson 1 , Michael M Timm 2 , Curtis A Hanson 2 , Daniel L Van Dyke 2 , Surendra Dasari 3 , Thomas E Witzig 1
Affiliation
Despite the unprecedented success of ibrutinib in lymphoma therapy, the development of ibrutinib resistance due to acquired BTK or PLCγ2 mutations has become a new clinical problem. However, not all resistance is mediated by these mutations and these mechanisms are poorly understood due to a lack of study tools that truly recapitulate this clinical scenario.
中文翻译:
MCIR1:一种源自患者的套细胞淋巴瘤细胞系,用于发现伊布替尼耐药的新疗法
尽管依鲁替尼在淋巴瘤治疗中取得了空前的成功,但由于获得性BTK或PLCγ2突变引起的依鲁替尼耐药性的发展已成为一个新的临床问题。然而,并非所有的耐药性都是由这些突变介导的,而且由于缺乏真正概括这种临床情况的研究工具,这些机制也知之甚少。
更新日期:2021-09-10
中文翻译:
MCIR1:一种源自患者的套细胞淋巴瘤细胞系,用于发现伊布替尼耐药的新疗法
尽管依鲁替尼在淋巴瘤治疗中取得了空前的成功,但由于获得性BTK或PLCγ2突变引起的依鲁替尼耐药性的发展已成为一个新的临床问题。然而,并非所有的耐药性都是由这些突变介导的,而且由于缺乏真正概括这种临床情况的研究工具,这些机制也知之甚少。