Open AccessCarbon Disulfide (CS2) Induced Chromosomal Alterations and Apoptosis in Circulated Blood Lymphocytes of Personnel Working in Viscose Industry
Author(s) -
Manikantan Pappuswamy,
Rajkumar Sundaram,
Harishankar M Kuppanna,
Thirunavukkarasu Periyasamy
Publication year - 2018
Publication title -
asian pacific journal of cancer biology
Language(s) - English
Resource type - Journals
ISSN - 2538-4635
DOI - 10.31557/apjcb.2018.3.1.17-24
Subject(s) - sister chromatid exchange , carbon disulfide , genotoxicity , apoptosis , flow cytometry , dna damage , comet assay , chemistry , toxicology , sister chromatids , andrology , lymphocyte , microbiology and biotechnology , genetics , immunology , dna , medicine , biology , biochemistry , toxicity , gene , chromosome , organic chemistry
Background and objective: Carbon disulfide (CS2) is a naturally occurring chemical substance in the environment and also an important endogenous substance in the human body. This study was done to collect data on the effects and to find a possible relationship between in-vivo CS2 induced apoptosis and genotoxic effects.Material and method: Circulated blood lymphocytes (PBL) of 41 workers occupationally exposed to Carbon disulfide (CS2) in viscose industry were investigated. The participants involved three groups. The first group included 41 participants exposed to CS2 together with various confounding factors; the second group comprised of 41 participants who were inhabitant of viscose industry and were partially exposed to CS2 in long periods; and third group consisting 41 participants as control group who were not exposed to any kind of chemicals and radiation hazards. Ambient air concentrations of CS2 were measured in different workplaces. Measures of genotoxicity included the determination of the frequencies of chromosomal aberrations (CA), sister-chromatid exchange (SCE), HPRT mutations (variant frequency, VF), and measurement of UV-induced unscheduled DNA-repair synthesis (UDS). The percentages of premature centromere division (PCD) and of cells with a high frequency of SCE (HF/SCE) were also scored. Apoptosis and c l proliferation were determined by flow cytometry.Results: In both CS2 exposed groups, the apoptotic activity and the CA levels in PBLs were significantly higher than in controls. CA was mostly breaks of the chromatid type. In group II, CA was slightly lower in comparison with group I, which can be attributed to a different rate of elimination of damaged lymphocytes as a consequence of CS2 induced apoptotic activity.Conclusion: The results demonstrate that exposure to CS2 induced apoptosis and CA, indicating an excess cancer risk among participants occupationally exposed to CS2. The results also emphasized the importance of the measurement of occupationally exposed pollutants such as CS2 in order to avoid genotoxic effects in the workers.