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Coal tar pitch extract could induce chromosomal instability of human bronchial epithelial cells mediated by spindle checkpoint-related proteins

机译:煤焦油沥青提取物可诱导纺锤体检查点相关蛋白介导的人支气管上皮细胞染色体不稳定

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摘要

Coal tar pitch (CTP) is a byproduct of coal tar distillation. The workers working with coal tar or in aluminum smelters, potrooms and carbon plants have the opportunities of exposing to coal tar pitch volatiles. Coal tar pitches from which polycyclic aromatic hydrocarbons (PAHs) originate have been shown to exhibit lung carcinogenicity in humans. Chromosomal instability (CIN) is a mechanism in carcinogenesis, however, whether CIN is involved in coal tar pitch-induced lung cancer remains elusive. In this present study, human bronchial epithelial cells (BEAS-2B) were first exposed to coal tar pitch extracts (CTPE) to induce a malignant transformation model. Then, the occurrence of severe chromosomal changes detected using G band, R band and multiplex fluorescence in situ hybridization (M-FISH) staining were examined. It was shown that more clones of transformed BEAS-2B cells at passage 30 following stimulation with CTPE were formed in the soft agar compared with the vehicle control. Moreover, the expression of the spindle checkpoint-related proteins, mitotic arrest defective 2 (Mad2), budding uninhibited in benzimidazole 1 (Bub1), and anaphase-promoting complex (APC), indicators of abnormal chromosomes and carcinogenesis, reduced in CTPE-treated BEAS-2B cells at Passage 30 compared with the vehicle control using real-time PCR and immunohistochemistry. In summary, exposure of BEAS-2B cells to CTPE may induce chromosomal instability through spindle checkpoint-related proteins.
机译:煤焦油沥青(CTP)是煤焦油蒸馏的副产物。在煤焦油或铝冶炼厂,车间和碳工厂中工作的工人有机会接触煤焦油沥青挥发物。多环芳烃(PAHs)来源的煤焦油沥青已显示出对人类的肺致癌性。染色体不稳定性(CIN)是致癌作用的机制,但是,CIN是否参与煤焦油沥青诱导的肺癌仍不清楚。在本研究中,首先将人支气管上皮细胞(BEAS-2B)暴露于煤焦油沥青提取物(CTPE)以诱导恶性转化模型。然后,检查了使用G条带,R条带和多重荧光原位杂交(M-FISH)染色检测到的严重染色体变化的发生。结果表明,与载剂对照相比,在CTPE刺激后的第30代中,在软琼脂中形成了更多的转化BEAS-2B细胞克隆。此外,经CTPE处理后,纺锤体检查点相关蛋白,有丝分裂阻滞缺陷2(Mad2),苯并咪唑1(Bub1)中不受抑制的出芽和后期促进复合物(APC)的表达,异常染色体的指示和致癌作用在CTPE处理中均降低与使用实时PCR和免疫组织化学的媒介物对照相比,第30代的BEAS-2B细胞。总之,将BEAS-2B细胞暴露于CTPE可能会通过纺锤体检查点相关蛋白诱导染色体不稳定。

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