网络驱动的癌细胞化身,用于 DNA 损伤反应抑制剂的组合发现和生物标记物鉴定。

IF 3.5 2区 生物学 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Orsolya Papp, Viktória Jordán, Szabolcs Hetey, Róbert Balázs, Valér Kaszás, Árpád Bartha, Nóra N Ordasi, Sebestyén Kamp, Bálint Farkas, Jerome Mettetal, Jonathan R Dry, Duncan Young, Ben Sidders, Krishna C Bulusu, Daniel V Veres
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引用次数: 0

摘要

联合疗法已被公认为癌症治疗的关键干预策略,有可能克服单一疗法的抗药性并提供更持久的疗效。然而,鉴于尚未开发的潜在靶点空间的规模以及由此产生的组合爆炸,确定有效的药物组合是一个关键的未满足需求,这一需求仍在不断发展。在本文中,我们展示了一种由网络生物学驱动、基于模拟的解决方案--Simulated Cell™。通过将 omics 数据与经过策划的信号传导网络整合在一起,我们可以准确、可解释地预测从大规模组合药物敏感性筛选中获得的横跨 97 个癌症细胞系的 684 种组合的 66,348 对组合-细胞系配对(BAC = 0.62,AUC = 0.7)。我们强调了与 DNA 损伤反应通路相互作用并被预测为具有协同作用的药物组合对,并通过深入的网络洞察来确定驱动组合协同作用的生物标志物。我们证明,癌细胞 "化身 "捕捉到了其体外对应物的生物复杂性,从而能够识别联合用药的通路级机制,为临床转化提供指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Network-driven cancer cell avatars for combination discovery and biomarker identification for DNA damage response inhibitors.

Network-driven cancer cell avatars for combination discovery and biomarker identification for DNA damage response inhibitors.

Combination therapy is well established as a key intervention strategy for cancer treatment, with the potential to overcome monotherapy resistance and deliver a more durable efficacy. However, given the scale of unexplored potential target space and the resulting combinatorial explosion, identifying efficacious drug combinations is a critical unmet need that is still evolving. In this paper, we demonstrate a network biology-driven, simulation-based solution, the Simulated Cell™. Integration of omics data with a curated signaling network enables the accurate and interpretable prediction of 66,348 combination-cell line pairs obtained from a large-scale combinatorial drug sensitivity screen of 684 combinations across 97 cancer cell lines (BAC = 0.62, AUC = 0.7). We highlight drug combination pairs that interact with DNA Damage Response pathways and are predicted to be synergistic, and deep network insight to identify biomarkers driving combination synergy. We demonstrate that the cancer cell 'avatars' capture the biological complexity of their in vitro counterparts, enabling the identification of pathway-level mechanisms of combination benefit to guide clinical translatability.

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来源期刊
NPJ Systems Biology and Applications
NPJ Systems Biology and Applications Mathematics-Applied Mathematics
CiteScore
5.80
自引率
0.00%
发文量
46
审稿时长
8 weeks
期刊介绍: npj Systems Biology and Applications is an online Open Access journal dedicated to publishing the premier research that takes a systems-oriented approach. The journal aims to provide a forum for the presentation of articles that help define this nascent field, as well as those that apply the advances to wider fields. We encourage studies that integrate, or aid the integration of, data, analyses and insight from molecules to organisms and broader systems. Important areas of interest include not only fundamental biological systems and drug discovery, but also applications to health, medical practice and implementation, big data, biotechnology, food science, human behaviour, broader biological systems and industrial applications of systems biology. We encourage all approaches, including network biology, application of control theory to biological systems, computational modelling and analysis, comprehensive and/or high-content measurements, theoretical, analytical and computational studies of system-level properties of biological systems and computational/software/data platforms enabling such studies.
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