We characterized cytogenetic, hematological, and immunophenotypic status in two female gas station attendants, who working in gas station with a proved harmful enviromental concentration of BTX. The following abnormalities were found: CCRs, a decrease in NK cells with abnormal CD16 expression, and early pregnancy loss.
It is well known that gas station workers are exposed to potentially harmful chemicals including BTX. However, benzene is considered the main carcinogenic agent (group 1 according to IARC) and studies associate this compound with acquired cytogenetic alterations [5,6,7]. Among various forms of benzene-induced genetic alterations, aneuploidy and chromosomal breakage are the most studied [4]. Chromosomal aberrations in peripheral blood lymphocytes of chronically benzene-exposed patients were previously documented [5,6,7]. Zhang et al. [5] reported dose-dependent chromosomal aneuploidies (mono- and trisomies) in the peripheral blood lymphocytes of workers exposed to benzene. In our study, we analyzed CAs only in three pairs of chromosomes, which make up 22.8% of the human genome. It’s a cheaper and faster test to estimate the DNA damage when compared to whole genome CA screening. Chromosomal aberrations (CAs) of high complexities could be detected in 1 out of 100 metaphases per patient (i.e. 1%). The rate of CCRs in normal controls lies between 0 and 0.5%, determined in 1000 metaphases, each [8]. In the present study, only 100 metaphases could be analyzed per case. Thus, the finding of one meta- phase with a CCR among 100 cells is at least noteworthy.
Even though CCR detection in peripheral blood is not directly correlated with enhanced cancer risk, it should be kept in mind that such CAs may indicate increased radio- and/or chemosensitivity. As tumors may be induced by environmental factors in combination with a special genetic susceptibility, the two cases reported may be at risk of acquiring malignancies [8].
As is well known, meiosis is a complex process controlled by different checkpoints, but males and females respond differently to meiotic disturbances [9]. During oogenesis, meiosis is generally pursued leading to the formation of aneuploid gametes or with single gene mutations.
Thus, in gametes, acquired genetic changes can be passed on to the next generation. Several epidemiological studies support the idea that genotoxic and nongenotoxic events following benzene exposure may be initiators of childhood leukemia in utero [10]. Another study on AML has shown that disease is usually initiated in utero because the leukemic translocations and other genetic changes are present in blood spots collected at birth [10, 11]. Also interesting is the fact that the majority of the CCR cases are reported in females ascertained through repeated spontaneous abortions or the birth of a malformed child [11].
Besides the detected CCRs pointing towards enhanced chemosensitivity, these two female workers had hematological and immunological abnormalities characterized by mild leukopenia (case 1) and NK abnormalities. There are some studies concerning benzene with hematological and immunological abnormalities in humans [12,13,14,15,16]. The effects of immunotoxicity induced by benzene are depression and alteration of both the immune system mediated by cells and the humoral system [15]. Lan et al. [13] observed that leucocytes, B and CD4+-T cell counts, were significantly decreased in workers exposed to benzene compared to the controls. In another study, the number of T lymphocytes, lymphocytes T CD4 and T CD8, and NK cells was reduced in the percentages and absolute numbers, and an increase in the monocyte count in workers during the period of exposure was found [15]. Thus, it was suggested that the depressive effect of benzene on the T and NK cells may be a factor of the probable carcinogenic activity of benzene through the immune system.
Natural killer (NK) cells are immune effector cells that recognize both virally infected and malignant target cells. Surprisingly, the results of the immunophenotypic analysis revealed NK CD56 positive (normal fluorescence) and CD16 negative in both cases, suggesting the presence of the rare subtype NK bright in the peripheral blood, which has low cytotoxic action [15]. It is possible that the action of BTX on the immune system had blocked the transition of immature CD56 bright cells into CD56 dim cells. In agreement with this finding, an 11 year follow up study showed that low NK cytotoxicity of peripheral blood lymphocytes correlates with an increased risk for cancer [16].
The identifications of chromosomal abnormalities and NK downregulation in the blood may be a new indicator for effective follow up of workers exposed to BTX, preventing diseases mainly important for females and their offspring. Further studies with a larger number of workers are necessary to confirm the results found.
