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芳香烃受体激活至乳腺癌相关死亡的不良结局途径。

Adverse outcome pathway from activation of the AhR to breast cancer-related death.

机构信息

Université Paris Cité, T3S, INSERM UMR-S 1124, 45 rue des Saints Pères, Paris, France; Assistance Publique-Hôpitaux de Paris, European Hospital Georges-Pompidou, Gynecologic and Breast Oncologic Surgery Department, Paris, France.

Université Paris Cité, T3S, INSERM UMR-S 1124, 45 rue des Saints Pères, Paris, France.

出版信息

Environ Int. 2022 Jul;165:107323. doi: 10.1016/j.envint.2022.107323. Epub 2022 May 28.

DOI:10.1016/j.envint.2022.107323
PMID:35660951
Abstract

Adverse outcome pathways (AOPs) are formalized and structured linear concepts that connect one molecular initiating event (MIE) to an adverse outcome (AO) via different key events (KE) through key event relationships (KER). They are mainly used in eco-toxicology toxicology, and regulatory health issues. AOPs must respond to specific guidelines from the Organization for Economic Co-operation and Development (OECD) to weight the evidence between each KE. Breast cancer is the deadliest cancer in women with a poor prognosis in case of metastatic breast cancer. The role of the environments in the formation of metastasis has been suggested. We hypothesized that activation of the AhR (MIE), a xenobiotic receptor, could lead to breast cancer related death (AO), through different KEs, constituting a new AOP. An artificial intelligence tool (AOP-helpfinder), which screens the available literature, was used to collect all existing scientific abstracts to build a novel AOP, using a list of key words. Four hundred and seven abstracts were found containing at least a word from our MIE list and either one word from our AO or KE list. A manual curation retained 113 pertinent articles, which were also screened using PubTator. From these analyses, an AOP was created linking the activation of the AhR to breast cancer related death through decreased apoptosis, inflammation, endothelial cell migration, angiogenesis, and invasion. These KEs promote an increased tumor growth, angiogenesis and migration which leads to breast cancer metastasis and breast cancer related death. The evidence of the proposed AOP was weighted using the tailored Bradford Hill criteria and the OECD guidelines. The confidence in our AOP was considered strong. An in vitro validation must be carried out, but our review proposes a strong relationship between AhR activation and breast cancer-related death with an innovative use of an artificial intelligence literature search.

摘要

不利结局途径 (AOP) 是将一个分子起始事件 (MIE) 通过关键事件关系 (KER) 连接到一个不利结局 (AO) 的形式化和结构化的线性概念。它们主要用于生态毒理学、毒理学和监管健康问题。AOP 必须响应经济合作与发展组织 (OECD) 的特定准则,以权衡每个 KE 之间的证据权重。乳腺癌是女性中最致命的癌症,如果发生转移性乳腺癌,预后很差。环境在转移形成中的作用已被提出。我们假设,一种外源性受体 AhR 的激活(MIE)可能导致与乳腺癌相关的死亡(AO),通过不同的 KE,构成一个新的 AOP。一种人工智能工具 (AOP-helpfinder) 被用来筛选现有的文献,以收集所有现有的科学摘要,使用关键词列表来构建一个新的 AOP。发现了 407 篇摘要,其中至少包含我们 MIE 列表中的一个词,并且包含我们 AO 或 KE 列表中的一个词。通过手动编辑,保留了 113 篇相关文章,并使用 PubTator 对其进行了筛选。从这些分析中,创建了一个 AOP,将 AhR 的激活与乳腺癌相关的死亡联系起来,通过减少细胞凋亡、炎症、内皮细胞迁移、血管生成和侵袭。这些 KE 促进肿瘤生长、血管生成和迁移的增加,导致乳腺癌转移和乳腺癌相关的死亡。使用定制的布拉德福德-希尔标准和 OECD 指南对所提出的 AOP 的证据进行了权重评估。我们的 AOP 的置信度被认为是很强的。必须进行体外验证,但我们的综述提出了 AhR 激活与乳腺癌相关死亡之间的强烈关系,并创新性地使用了人工智能文献搜索。

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