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新冠病毒病(COVID-19)和胃肠道癌症的共同促成因素。

Contributing factors common to COVID‑19 and gastrointestinal cancer.

作者信息

Kostoff Ronald Neil, Briggs Michael Brandon, Kanduc Darja, Shores Darla Roye, Kovatsi Leda, Drakoulis Nikolaos, Porter Alan Leslie, Tsatsakis Aristidis, Spandidos Demetrios A

机构信息

School of Public Policy, Georgia Institute of Technology, Gainesville, VA 20155, USA.

Independent Consultant, Roscommon, MI 48653, USA.

出版信息

Oncol Rep. 2022 Jan;47(1). doi: 10.3892/or.2021.8227. Epub 2021 Nov 15.

Abstract

The devastating complications of coronavirus disease 2019 (COVID‑19) result from the dysfunctional immune response of an individual following the initial severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) infection. Multiple toxic stressors and behaviors contribute to underlying immune system dysfunction. SARS‑CoV‑2 exploits the dysfunctional immune system to trigger a chain of events, ultimately leading to COVID‑19. The authors have previously identified a number of contributing factors (CFs) common to myriad chronic diseases. Based on these observations, it was hypothesized that there may be a significant overlap between CFs associated with COVID‑19 and gastrointestinal cancer (GIC). Thus, in the present study, a streamlined dot‑product approach was used initially to identify potential CFs that affect COVID‑19 and GIC directly (i.e., the simultaneous occurrence of CFs and disease in the same article). The nascent character of the COVID‑19 core literature (~1‑year‑old) did not allow sufficient time for the direct effects of numerous CFs on COVID‑19 to emerge from laboratory experiments and epidemiological studies. Therefore, a literature‑related discovery approach was used to augment the COVID‑19 core literature‑based 'direct impact' CFs with discovery‑based 'indirect impact' CFs [CFs were identified in the non‑COVID‑19 biomedical literature that had the same biomarker impact pattern (e.g., hyperinflammation, hypercoagulation, hypoxia, etc.) as was shown in the COVID‑19 literature]. Approximately 2,250 candidate direct impact CFs in common between GIC and COVID‑19 were identified, albeit some being variants of the same concept. As commonality proof of concept, 75 potential CFs that appeared promising were selected, and 63 overlapping COVID‑19/GIC potential/candidate CFs were validated with biological plausibility. In total, 42 of the 63 were overlapping direct impact COVID‑19/GIC CFs, and the remaining 21 were candidate GIC CFs that overlapped with indirect impact COVID‑19 CFs. On the whole, the present study demonstrates that COVID‑19 and GIC share a number of common risk/CFs, including behaviors and toxic exposures, that impair immune function. A key component of immune system health is the removal of those factors that contribute to immune system dysfunction in the first place. This requires a paradigm shift from traditional Western medicine, which often focuses on treatment, rather than prevention.

摘要

2019冠状病毒病(COVID-19)的毁灭性并发症源于个体在初次感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)后功能失调的免疫反应。多种毒性应激源和行为导致潜在的免疫系统功能障碍。SARS-CoV-2利用功能失调的免疫系统引发一系列事件,最终导致COVID-19。作者此前已经确定了许多常见慢性病共有的一些促成因素(CFs)。基于这些观察结果,研究人员推测,与COVID-19相关的CFs和胃肠道癌(GIC)之间可能存在显著重叠。因此,在本研究中,最初使用了一种简化的点积方法来识别直接影响COVID-19和GIC的潜在CFs(即同一篇文章中CFs和疾病的同时出现)。COVID-19核心文献(约1年历史)的新生特性使得众多CFs对COVID-19的直接影响没有足够的时间从实验室实验和流行病学研究中显现出来。因此,采用了一种与文献相关的发现方法,用基于发现的“间接影响”CFs(在非COVID-19生物医学文献中识别出的CFs与COVID-19文献中显示的具有相同生物标志物影响模式,如炎症过度、凝血过度、缺氧等)来补充基于COVID-19核心文献的“直接影响”CFs。尽管有些是同一概念的变体,但在GIC和COVID-19之间共识别出约2250个候选直接影响CFs。作为概念共性的证明,选择了75个看起来有前景的潜在CFs,并通过生物学合理性验证了63个重叠的COVID-19/GIC潜在/候选CFs。在这63个中,总共有42个是重叠的直接影响COVID-19/GIC的CFs,其余21个是与间接影响COVID-19的CFs重叠的候选GIC CFs。总体而言,本研究表明,COVID-19和GIC有许多共同的风险/CFs,包括损害免疫功能的行为和有毒暴露。免疫系统健康的一个关键组成部分是首先消除那些导致免疫系统功能障碍的因素。这需要从通常侧重于治疗而非预防的传统西医模式转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/075e/8611322/2c6b57bd05e6/or-47-01-08227-g00.jpg

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