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压力与癌症:机制、意义及未来方向。

Stress and cancer: mechanisms, significance and future directions.

作者信息

Eckerling Anabel, Ricon-Becker Itay, Sorski Liat, Sandbank Elad, Ben-Eliyahu Shamgar

机构信息

Sagol School of Neuroscience and School of Psychological Sciences, Tel Aviv University, Tel Aviv, Israel.

出版信息

Nat Rev Cancer. 2021 Dec;21(12):767-785. doi: 10.1038/s41568-021-00395-5. Epub 2021 Sep 10.

Abstract

The notion that stress and cancer are interlinked has dominated lay discourse for decades. More recent animal studies indicate that stress can substantially facilitate cancer progression through modulating most hallmarks of cancer, and molecular and systemic mechanisms mediating these effects have been elucidated. However, available clinical evidence for such deleterious effects is inconsistent, as epidemiological and stress-reducing clinical interventions have yielded mixed effects on cancer mortality. In this Review, we describe and discuss specific mediating mechanisms identified by preclinical research, and parallel clinical findings. We explain the discrepancy between preclinical and clinical outcomes, through pointing to experimental strengths leveraged by animal studies and through discussing methodological and conceptual obstacles that prevent clinical studies from reflecting the impacts of stress. We suggest approaches to circumvent such obstacles, based on targeting critical phases of cancer progression that are more likely to be stress-sensitive; pharmacologically limiting adrenergic-inflammatory responses triggered by medical procedures; and focusing on more vulnerable populations, employing personalized pharmacological and psychosocial approaches. Recent clinical trials support our hypothesis that psychological and/or pharmacological inhibition of excess adrenergic and/or inflammatory stress signalling, especially alongside cancer treatments, could save lives.

摘要

压力与癌症相互关联这一观念在大众话语中占据主导地位已有数十年。最近的动物研究表明,压力可通过调节癌症的大多数特征显著促进癌症进展,并且介导这些效应的分子和全身机制已得到阐明。然而,关于这种有害影响的现有临床证据并不一致,因为流行病学和减轻压力的临床干预对癌症死亡率产生了混合效应。在本综述中,我们描述并讨论了临床前研究所确定的具体介导机制以及相应的临床研究结果。我们通过指出动物研究所利用的实验优势,并讨论阻碍临床研究反映压力影响的方法学和概念性障碍,来解释临床前和临床结果之间的差异。我们建议通过针对癌症进展中更可能对压力敏感的关键阶段;从药理学上限制医疗程序引发的肾上腺素能 - 炎症反应;以及关注更脆弱的人群,采用个性化的药理学和心理社会方法等途径来规避这些障碍。最近的临床试验支持了我们的假设,即对过度的肾上腺素能和/或炎症应激信号进行心理和/或药理学抑制,尤其是在癌症治疗期间,可能挽救生命。

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