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生成用于临床前研究的胶质母细胞瘤患者来源颅内异种移植物。

Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies.

机构信息

Department of Neurological Surgery, Case Western Reserve University and University Hospitals Cleveland, OH 44106, USA.

Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Int J Mol Sci. 2020 Jul 20;21(14):5113. doi: 10.3390/ijms21145113.

Abstract

Glioblastoma multiforme (GBM) is the most malignant primary brain cancer affecting adults. Therapeutic options for GBM have remained the same for over a decade with no significant improvement. Many therapies that are successful in culture have failed in patients, likely due to the complex microenvironment in the brain, which has yet to be reproduced in any culture model. Furthermore, the high passage number of cultured cells and clonal selection fail to recapitulate the molecular and genomic signatures of GBM. We have established orthotopic patient-derived xenografts (PDX) from 37 GBM patients with human GBM. Of the 69 patient samples analyzed, we were successful in passaging 37 lines three or more generations (53.6%). After phenotypic characterization of the xenografted tumor tissue, two different growth patterns emerged highly invasive or localized. The phenotype was dependent on malignancy and previous treatment of the patient from which the xenograft was derived. Physiologically, mice exhibited symptoms more quickly with each subsequent passage, particularly in the localized tumors. Study of these physiologically relevant human xenografts in mice will enable therapeutic screenings in a microenvironment that more closely resembles GBM and may allow development of individualized patient models which may eventually be used for simulating treatment.

摘要

多形性胶质母细胞瘤(GBM)是影响成年人的最恶性原发性脑癌。GBM 的治疗选择十年来一直没有改变,没有显著改善。许多在培养中成功的疗法在患者中失败了,这可能是由于大脑中复杂的微环境尚未在任何培养模型中重现。此外,培养细胞的高传代数和克隆选择未能重现 GBM 的分子和基因组特征。我们从 37 名 GBM 患者中建立了原位患者来源的异种移植物(PDX)。在分析的 69 个患者样本中,我们成功地传代了 37 条线三代或三代以上(53.6%)。在异种移植肿瘤组织的表型特征分析后,出现了两种不同的生长模式:高度侵袭性或局限性。表型取决于肿瘤的恶性程度和患者的先前治疗。在生理上,随着每一次后续传代,老鼠的症状出现得更快,尤其是在局限性肿瘤中。在小鼠中研究这些生理相关的人源异种移植物将能够在更接近 GBM 的微环境中进行治疗筛选,并可能开发出个体化的患者模型,最终可能用于模拟治疗。

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