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苯代谢产物对苯二酚和苯三酚诱导的1、5、6、7、8、9、11、12和21号染色体的非随机非整倍性。

Nonrandom aneuploidy of chromosomes 1, 5, 6, 7, 8, 9, 11, 12, and 21 induced by the benzene metabolites hydroquinone and benzenetriol.

作者信息

Zhang Luoping, Yang Wei, Hubbard Alan E, Smith Martyn T

机构信息

Division of Environmental Health Sciences, School of Public Health, University of California, Berkeley, California 94720, USA.

出版信息

Environ Mol Mutagen. 2005 May;45(4):388-96. doi: 10.1002/em.20103.

Abstract

The loss and gain of whole chromosomes (aneuploidy) is common in the development of leukemia and other cancers. In acute myeloid leukemia, the loss (monosomy) of chromosomes 5 and 7 and the gain (trisomy) of chromosome 8 are common clonal chromosomal abnormalities. Here, we have tested the hypothesis that metabolites of the human leukemogen benzene cause a higher rate of gain and loss among the chromosomes involved in leukemogenesis and, as such, are nonrandom and selective in their effects. Human peripheral blood was exposed to two metabolites of benzene, namely, hydroquinone (HQ) and benzenetriol (BT), and the ploidy status of nine different chromosomes (1, 5, 6, 7, 8, 9, 11, 12, and 21) was examined using fluorescence in situ hybridization of metaphase spreads. Poisson regression was used to provide interpretable incidence rate ratios and corresponding P values for all nine chromosomes. Statistically significant differences were found between the sensitivity of the nine chromosomes to gain or loss. Chromosomes 5 and 7 were highly sensitive to loss following HQ and BT exposure, whereas chromosomes 7, 8, and 21 were highly sensitive to gain in comparison to other chromosomes. Significant support for the a priori hypothesis that chromosomes 5 and 7 are more sensitive to loss induced by HQ and BT than the other seven chromosomes was also obtained. These data support the notion that benzene metabolites affect the ploidy status of specific chromosomes more than others and may initiate or promote leukemia induction through these specific effects.

摘要

整条染色体的丢失和增加(非整倍性)在白血病和其他癌症的发展过程中很常见。在急性髓系白血病中,5号和7号染色体的丢失(单体性)以及8号染色体的增加(三体性)是常见的克隆性染色体异常。在此,我们检验了这样一个假设:人类白血病致癌物苯的代谢产物会导致白血病发生过程中涉及的染色体出现更高频率的增减,并且其作用具有非随机性和选择性。将人类外周血暴露于苯的两种代谢产物,即对苯二酚(HQ)和苯三酚(BT),并使用中期染色体铺展的荧光原位杂交技术检测九条不同染色体(1、5、6、7、8、9、11、12和21)的倍性状态。采用泊松回归分析为所有九条染色体提供可解释的发病率比值及相应的P值。结果发现九条染色体在增减敏感性方面存在统计学显著差异。暴露于HQ和BT后,5号和7号染色体对丢失高度敏感,而与其他染色体相比,7号、8号和21号染色体对增加高度敏感。同时也获得了有力证据支持先验假设,即5号和7号染色体比其他七条染色体对HQ和BT诱导的丢失更敏感。这些数据支持了这样一种观点,即苯代谢产物对特定染色体倍性状态的影响大于其他染色体,并可能通过这些特定作用引发或促进白血病的发生。

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