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MKC8866 通过抑制 IRE1 实现局部脑内抑制,从而增强体内胶质母细胞瘤对放疗/化疗的敏感性。

Local intracerebral inhibition of IRE1 by MKC8866 sensitizes glioblastoma to irradiation/chemotherapy in vivo.

机构信息

Inserm U1242, University of Rennes, Rennes, France; Centre de lutte contre le cancer Eugène Marquis, Rennes, France; Rennes Brain Cancer Team (REACT), 35000, Rennes, France; Neurosurgery Dept, University Hospital of Rennes, 35000, Rennes, France.

Inserm U1242, University of Rennes, Rennes, France; Centre de lutte contre le cancer Eugène Marquis, Rennes, France; Rennes Brain Cancer Team (REACT), 35000, Rennes, France.

出版信息

Cancer Lett. 2020 Dec 1;494:73-83. doi: 10.1016/j.canlet.2020.08.028. Epub 2020 Sep 1.

Abstract

Glioblastoma multiforme (GBM) is the most severe primary brain cancer. Despite an aggressive treatment comprising surgical resection and radio/chemotherapy, patient's survival post diagnosis remains short. A limitation for success in finding novel improved therapeutic options for such dismal disease partly lies in the lack of a relevant animal model that accurately recapitulates patient disease and standard of care. In the present study, we have developed an immunocompetent GBM model that includes tumor surgery and a radio/chemotherapy regimen resembling the Stupp protocol and we have used this model to test the impact of the pharmacological inhibition of the endoplasmic reticulum (ER) stress sensor IRE1, on treatment efficacy.

摘要

多形性胶质母细胞瘤(GBM)是最严重的原发性脑癌。尽管采用了包括手术切除、放射/化疗在内的积极治疗方案,但患者的诊断后生存时间仍然很短。在寻找新的改善这种疾病治疗方法的过程中,部分原因是缺乏能够准确再现患者疾病和标准治疗的相关动物模型。在本研究中,我们开发了一种免疫活性 GBM 模型,包括肿瘤手术和类似于 Stupp 方案的放射/化疗方案,我们使用该模型来测试内质网(ER)应激传感器 IRE1 的药理学抑制对治疗效果的影响。

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