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Evaluation of cell types for assessment of cytogenetic damage in arsenic exposed population

DOI: 10.1186/1476-4598-7-45

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Abstract:

For literature review, we have searched the Pubmed database for English language journal articles using the following keywords: "arsenic", "micronuclei", "drinking water", and "human" in various combinations. We have selected 13 studies consistent with our inclusion criteria that measured micronuclei in either one or more of the above-mentioned three cell types, in human samples. Compared to urothelial and buccal mucosa cells, the median effect sizes measured by the difference between people with exposed and unexposed, lymphocyte based MN counts were found to be stronger. This general pattern pooled from 10 studies was consistent with our own set of three earlier studies. MN counts were also found to be stronger for lymphocytes even in arsenic-induced Bowen's patients (cases) compared to control individuals having arsenic-induced non-cancerous skin lesions.Overall, it can be concluded that MN in lymphocytes may be superior to other epithelial cells for studying arsenic-induced cytogenetic damage.Exposure to inorganic arsenic through drinking water results in cancers of skin, urinary bladder, liver and the lungs. Cytogenetic assays play an important role in toxicological hazard evaluation as the first step towards quantification of cancers. Various genetic toxicological end-points have been used as biomarkers to understand the biological effects of arsenic exposure [1]. Biomarkers serve as internal indicators of environmental or occupational exposures and have the potential for prevention of effects of carcinogen exposure by early detection [2]. Micronuclei are the potential biomarkers and traditionally been used for biomonitoring of genotoxic effects in humans [3]. Micronuclei are chromosomal fragments or the whole chromosomes that are not included in to the daughter nuclei during cell division and are incorporated as much smaller nuclei. The formation of MN is therefore induced by substances that cause breakage of chromosomes (clastogens) as well as by agents, whic

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