肿瘤医学治疗的个体化:是时候重新思考疾病概念以改善个体结果了。

IF 6.5 2区 医学 Q1 Medicine Epma Journal Pub Date : 2021-10-07 eCollection Date: 2021-12-01 DOI:10.1007/s13167-021-00254-1
Mariano Bizzarri, Valeria Fedeli, Noemi Monti, Alessandra Cucina, Maroua Jalouli, Saleh H Alwasel, Abdel Halim Harrath
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引用次数: 7

摘要

个性化肿瘤学领域的药理学发现议程是由寻找分子靶标决定的,这些靶标被认为是决定性地驱动肿瘤发展的。从这个角度来看,基因起着基本的“因果”作用,而细胞只是作为因果代理,即分子输入和有机体输出之间的中介。然而,随着时间的推移,在同一原发和转移性肿瘤中不断发生的基因组变化打破了仅基于基因组指纹进行个性化治疗的希望。事实上,目前的模型无法捕捉疾病爆发背后深不可测的复杂性,因为它们忽略了非遗传因素、环境约束和不同组织层次之间的相互作用。在此,我们假设一个全面的个性化模型应该将疾病视为一个“历史”过程,在这个过程中,不同的空间和时间分布的因素在多个组织层面上相互作用,这些因素共同与动态的基因表达模式相互作用。鉴于疾病是一个动态的、非线性的过程——而不是一个静态稳定的状态——治疗应该根据每种状态的“时间框架”来调整。这种方法可以帮助检测那些关键的转变,通过这些转变,系统可以接触到不同的吸引子,最终导致不同的结果——从疾病前的状态到明显的疾病状态,或者,或者,恢复。确定这些临界点可以证实预测、预防和个性化医学(PPPM/3PM)的预测和预防目标。然而,需要结合多组学方法、数据收集和网络分析重建(最终涉及创新的人工智能工具)来识别关键阶段和相关目标,这可能有助于患者分层和治疗个性化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Personalization of medical treatments in oncology: time for rethinking the disease concept to improve individual outcomes.

The agenda of pharmacology discovery in the field of personalized oncology was dictated by the search of molecular targets assumed to deterministically drive tumor development. In this perspective, genes play a fundamental "causal" role while cells simply act as causal proxies, i.e., an intermediate between the molecular input and the organismal output. However, the ceaseless genomic change occurring across time within the same primary and metastatic tumor has broken the hope of a personalized treatment based only upon genomic fingerprint. Indeed, current models are unable in capturing the unfathomable complexity behind the outbreak of a disease, as they discard the contribution of non-genetic factors, environment constraints, and the interplay among different tiers of organization. Herein, we posit that a comprehensive personalized model should view at the disease as a "historical" process, in which different spatially and timely distributed factors interact with each other across multiple levels of organization, which collectively interact with a dynamic gene-expression pattern. Given that a disease is a dynamic, non-linear process - and not a static-stable condition - treatments should be tailored according to the "timing-frame" of each condition. This approach can help in detecting those critical transitions through which the system can access different attractors leading ultimately to diverse outcomes - from a pre-disease state to an overt illness or, alternatively, to recovery. Identification of such tipping points can substantiate the predictive and the preventive ambition of the Predictive, Preventive and Personalized Medicine (PPPM/3PM). However, an unusual effort is required to conjugate multi-omics approaches, data collection, and network analysis reconstruction (eventually involving innovative Artificial Intelligent tools) to recognize the critical phases and the relevant targets, which could help in patient stratification and therapy personalization.

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来源期刊
Epma Journal
Epma Journal Medicine-Biochemistry (medical)
CiteScore
11.30
自引率
23.10%
发文量
0
期刊介绍: PMA Journal is a journal of predictive, preventive and personalized medicine (PPPM). The journal provides expert viewpoints and research on medical innovations and advanced healthcare using predictive diagnostics, targeted preventive measures and personalized patient treatments. The journal is indexed by PubMed, Embase and Scopus.
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