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Neoplastic Transformation of Human Bronchial Cells by Lead Chromate Particles

机译:铬酸铅粒子对人支气管细胞的肿瘤转化

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摘要

Particulate hexavalent chromium (Cr(VI)) is a well-established human lung carcinogen with widespread exposure among people in occupational settings and the general public. However, no studies have examined the chromate-induced malignant transformation of human lung epithelial cells, its predominant target. Human papillomavirus–immortalized human bronchial epithelial (BEP2D) cells were used to better understand the mechanisms involved in human bronchial carcinogenesis induced by particulate chromate. We found that aneuploid cells increased in a concentration-dependent manner after chronic exposure to lead chromate. Moreover, chronic exposure to lead chromate induced BEP2D cell transformation. Transformed BEP2D cells developed through a series of sequential steps, including altered cell morphology, loss of cell contact inhibition and anchorage-independent growth. Specifically, a 5-day exposure to lead chromate induced foci formation with 0, 1, 5, and 10 μg/cm2 lead chromate inducing 0, 7, 3, and 15 foci in 10 dishes. Anchorage independence was observed in cell lines derived from these foci. These foci-derived cells also showed centrosome amplification and increases in aneuploid metaphases. Our study demonstrates that particulate Cr(VI) is able to transform human bronchial epithelial cells, and that chromosome instability may play an important role in particulate Cr(VI)-induced neoplastic transformation.
机译:六价铬颗粒(Cr(VI))是一种公认​​的人类肺致癌物,在职业环境和普通大众中广泛接触。但是,没有研究检查铬酸盐诱导的人肺上皮细胞(其主要靶标)的恶性转化。使用人乳头瘤病毒永生化的人支气管上皮细胞(BEP2D)可以更好地了解颗粒状铬酸盐诱导的人支气管癌变的机制。我们发现,慢性接触铬酸铅后,非整倍体细胞以浓度依赖的方式增加。此外,长期暴露于铬酸铅会诱导BEP2D细胞转化。转化的BEP2D细胞通过一系列连续步骤发育,包括改变的细胞形态,失去细胞接触抑制作用和不依赖锚定的生长。具体而言,暴露于铬酸铅的5天诱导了0、1、5和10μg/ cm 2 铬酸铅的灶形成,在10个皿中诱导了0、7、3和15灶。在源自这些病灶的细胞系中观察到了锚定独立性。这些灶源性细胞还显示了中心体扩增,并在非整倍体中期增加。我们的研究表明,微粒Cr(VI)能够转化人支气管上皮细胞,并且染色体不稳定可能在微粒Cr(VI)诱导的肿瘤转化中起重要作用。

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