机器学习辅助的临床前胶质瘤建模系统综述:实践是否随着时代而变化?

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-12-28 eCollection Date: 2024-01-01 DOI:10.1093/noajnl/vdae193
Theodore C Hirst, Emma Wilson, Declan Browne, Emily S Sena
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引用次数: 0

摘要

背景:尽管我们对胶质母细胞瘤病理生理的认识有所提高,但近年来在治疗方面没有重大进展。动物模型是研究癌症生物学及其治疗的重要工具,但也有已知的局限性。胶质母细胞瘤建模技术在本世纪取得了进展,尽管尚不清楚这些技术已被采用到何种程度。方法:我们使用旨在识别所有报道动物胶质瘤实验的出版物的术语检索Pubmed和EMBASE,使用机器学习算法辅助筛选。我们回顾了1000篇文章样本的全文,然后使用这些发现来显示所有包含的摘要,以评估整个数据集的建模应用程序。结果:检索到26 201篇出版物,其中13 783篇纳入筛选。自动筛选灵敏度高,但特异性有限。我们观察到传统细胞系范式的优势和先进肿瘤模型系统的出现被细胞系实验量的大量增加所掩盖。很少有研究在体内使用一个以上的模型,大多数出版物没有验证关键的遗传特征。结论:先进模型在肿瘤和疾病再现方面具有明显的优势,并且在很大程度上没有取代传统细胞系,传统细胞系存在许多严重缺陷,限制了它们在现代动物研究中的生存能力。明智地使用先进的模型或更多相关的细胞系可能会提高未来动物胶质母细胞瘤实验的翻译相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A machine learning-assisted systematic review of preclinical glioma modeling: Is practice changing with the times?

Background: Despite improvements in our understanding of glioblastoma pathophysiology, there have been no major improvements in treatment in recent years. Animal models are a vital tool for investigating cancer biology and its treatment, but have known limitations. There have been advances in glioblastoma modeling techniques in this century although it is unclear to what extent they have been adopted.

Methods: We searched Pubmed and EMBASE using terms designed to identify all publications reporting an animal glioma experiment, using a machine learning algorithm to assist with screening. We reviewed the full text of a sample of 1000 articles and then used the findings to inform a screen of all included abstracts to appraise the modeling applications across the entire dataset.

Results: The search identified 26 201 publications of which 13 783 were included at screening. The automated screening had high sensitivity but limited specificity. We observed a dominance of traditional cell line paradigms and the emergence of advanced tumor model systems eclipsed by a large increase in the volume of cell line experiments. Few studies used more than 1 model in vivo and most publications did not verify critical genetic features.

Conclusions: Advanced models have clear advantages in terms of tumor and disease recapitulation and have largely not replaced traditional cell lines which have a number of critical deficiencies that limit their viability in modern animal research. The judicious use of advanced models or more relevant cell lines might improve the translational relevance of future animal glioblastoma experimentation.

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CiteScore
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