Rafazi Parisasadat, Bagheri Zeinab, Haghi-Aminjan Hamed, Rahimifard Mahban, Ahvaraki Akram
Department of Cell and Molecular Biology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran 1983969411, Iran.
Pharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.
Toxicol Rep. 2024 Oct 1;13:101757. doi: 10.1016/j.toxrep.2024.101757. eCollection 2024 Dec.
Precancerous cells are present in all human bodies. Various environmental triggers can promote the development of cancer. Microplastics, an emerging concern, may potentially act as one such trigger, contributing to cancer initiation or progression. Studies have confirmed the presence of microplastics within the human body. This raises concerns about their potential toxicity and health risks. In the present study, we aimed to investigate the impact of polyethylene microplastics (PE-MPs) within the size range of 37-75 microns on glioblastoma cancer cells. Initially, we assessed the short-term effects of six different concentrations of PE-MPs (20 mg/mL, 10 mg/mL, 5 mg/mL, 2.5 mg/mL, 1.25 mg/mL, and 0.62 mg/mL) on the U87 glioblastoma cell line. The results demonstrated that PE-MPs exposure led to an increase in cell proliferation compared to the untreated control group. Based on these findings, we decided to further explore the long-term effects of PE-MPs on U87 cancer cells. To evaluate the long-term effects, U87 glioblastoma cells were continuously exposed to 0.005 g of PE-MPs over an extended period of 26 days. Chronic exposure to PE-MPs significantly increased the proliferative and migratory capacities of U87 cells compared to the unexposed control group. Furthermore, continuous PE-MPs exposure altered the behavior and morphological characteristics of U87 cells. These cells exhibited a propensity to aggregate and form colonies within the culture flask. The formation of spheroid structures was also observed in the PE-MPs-exposed cell population. The results of this research indicate that polyethylene microplastics can promote the progression of glioblastoma cancer.
癌前细胞存在于所有人的体内。各种环境诱因可促进癌症的发展。微塑料作为一个新出现的问题,可能会成为这样一种诱因,促使癌症发生或发展。研究已证实在人体内存有微塑料。这引发了人们对其潜在毒性和健康风险的担忧。在本研究中,我们旨在调查尺寸范围为37 - 75微米的聚乙烯微塑料(PE - MPs)对胶质母细胞瘤癌细胞的影响。最初,我们评估了六种不同浓度(20毫克/毫升、10毫克/毫升、5毫克/毫升、2.5毫克/毫升、1.25毫克/毫升和0.62毫克/毫升)的PE - MPs对U87胶质母细胞瘤细胞系的短期影响。结果表明,与未处理的对照组相比,暴露于PE - MPs会导致细胞增殖增加。基于这些发现,我们决定进一步探究PE - MPs对U87癌细胞的长期影响。为评估长期影响,U87胶质母细胞瘤细胞在26天的较长时间内持续暴露于0.005克PE - MPs。与未暴露的对照组相比,长期暴露于PE - MPs显著提高了U87细胞的增殖和迁移能力。此外,持续暴露于PE - MPs改变了U87细胞的行为和形态特征。这些细胞表现出在培养瓶内聚集并形成集落的倾向。在暴露于PE - MPs的细胞群体中还观察到了球体结构的形成。本研究结果表明,聚乙烯微塑料可促进胶质母细胞瘤癌症的发展。