细颗粒物(PM2.5)促进 A549 肺癌细胞的化疗抗性和侵袭性表型。

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2024-05-04 DOI:10.1016/j.taap.2024.116955
Zaira Colín-Val , Guillermo Flores-Navarro , Leticia Rocha-Zavaleta , Diana Xochiquetzal Robledo-Cadena , Raúl Omar Quintana-Belmares , Rebeca López-Marure
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引用次数: 0

摘要

肺癌是最具侵袭性的恶性肿瘤之一,死亡率很高。在大城市,颗粒物(PM)是一种常见的空气污染物。空气动力学尺寸≤2.5 μm(PM2.5)的高浓度可吸入颗粒物与肺癌的发病率和死亡率有关。在这项研究中,我们探讨了 PM2.5 对肺癌细胞行为的影响。为此,我们将 A549 细胞长期暴露于在墨西哥城收集到的浓度不断升高的 PM2.5,然后评估细胞增殖、化学反应、迁移、侵袭、球形体形成以及 P-糖蛋白和 N-粘连蛋白的表达。长期暴露于1微克/平方厘米的PM2.5会刺激A549细胞的增殖、迁移和化学抗性,并上调P-糖蛋白和N-粘附蛋白的表达。与对照细胞相比,PM2.5 还能诱导更大的多细胞肿瘤球(MCTS)和更少的崩解。因此,这些结果表明,暴露于空气中的城市污染物PM2.5的肺癌患者可能会发展出更具侵袭性的肿瘤表型,细胞增殖、迁移和化疗抵抗力增强。
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Fine particulate matter (PM2.5) promotes chemoresistance and aggressive phenotype of A549 lung cancer cells

Lung cancer is one of the most aggressive malignancies with a high mortality rate. In large cities, particulate matter (PM) is a common air pollutant. High PM levels with aerodynamic size ≤2.5 μm (PM2.5) associates with lung cancer incidence and mortality. In this work, we explored PM2.5 effects on the behavior of lung cancer cells. To this, we chronically exposed A549 cells to increasing PM2.5 concentrations collected in México City, then evaluating cell proliferation, chemoresponse, migration, invasion, spheroid formation, and P-glycoprotein and N-cadherin expression. Chronic PM2.5 exposure from 1 μg/cm2 stimulated A549 cell proliferation, migration, and chemoresistance and upregulated P-glycoprotein and N-cadherin expression. PM2.5 also induced larger multicellular tumor spheroids (MCTS) and less disintegration compared with control cells. Therefore, these results indicate lung cancer patients exposed to airborne PM2.5 as urban pollutant could develop more aggressive tumor phenotypes, with increased cell proliferation, migration, and chemoresistance.

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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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