Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
460<br />
_<br />
DETECTION OP MICRONUCLSI IN PERIPHERAL BLOOD LYMPHOCYTES OF PATIENTS WITH ESOPHAGEAL<br />
CANCER AND IMPROVEMENT OF THE METHOD . 2 . Qingfan, F . Shuli, <strong>and</strong> Y . Bin . Dept . of<br />
Pathology, Henan Medicaltniversity, 2hengzhou, Henan, P .R . China .<br />
Thirty-four cases of esophageal cancer were chosen for this study . Their age ranges<br />
from 30 to 75 . The diagnosis of the patients were confirmed by cytological examination<br />
in our department . They had not received radiotherapy, chemotherapy or other<br />
immunosuppressive agents recently . Thirty-four healthy persons were taken as the control .<br />
The method consists of taking 2 to 3 drops of blood from the ear lobe of the examined<br />
person, treating the blood sample with Tris-ammonium chloride buffer solution to hemolyze<br />
the red cells <strong>and</strong> then using the simplifled cytocentrifuge developed by the author to<br />
prepare the smears, the white cells can be concentrated <strong>and</strong> spread monolayerly onto a<br />
small area of the microscope slide, <strong>and</strong> the morphological details of the cells can be well<br />
preserved .' The background of the smear is clear, which facilitates scoring the<br />
micronuclei in lymphocytes . The normal range of micronuclei in lymphocytes in our study<br />
was 0-3 0/00 . It shows that the results of our improved method are similar to those with<br />
the ordinary method in which blood was taken by venous puncture . The improved method is<br />
not only fast <strong>and</strong> reliable, but liable to be accepted by the persona examined . The mean<br />
frequency of the micronuclei in the peripheral blood lymphocytes of the patients with<br />
esophageal cancer was 2 .8 0/00 as compared with 0 .832 0/00 in the control . The difference<br />
is statistically significant (p < 0 .001), but there is no marked specificity for the<br />
diagnosis of esophageal cancer, because the frequency in half of the patients with<br />
esophageal cancer is below 2 0/00, which superimposes with the control .<br />
461 The SOS Chromotest : an analysLs from published data on 430 chemio3ls.<br />
P . Quillardet, E. Touati <strong>and</strong> M. Hofnung . Institut Pasteur, UPMTG - CNRS UA271 - INSERM<br />
U 163 - Paris France .<br />
We have made use of an E. coli strain carrying a fusion of gene lacZ to gene 4fu1, one of the<br />
SOS gene, to devise a rapid assay for genotoxins : the SOS Chromotest (Quillardet et al ., Proc. Natl .<br />
Acad. Sci ., 79 : 5971, 1982 ; Mutation Res . 147: 65, 1985). The assay is performed in few hours <strong>and</strong><br />
involves simple enzymatic assays . It allows to classify compounds according to their SOS inducing<br />
potency (SOSIP), defined as their ability to induce the expression af the sfGl : aacZ fusion. To day,<br />
works from a number of laboratories using the SOS Chromotest have been published . We have<br />
reviewed data obtained with the SOS Chromotest on 430 chemicals issued from 40 publications arising<br />
from 20 different laboratories . This led us to evaluate further the potential of the SOS Chromotest to<br />
detect carcinogens <strong>and</strong> to compare its response to that of the Salmonella / microsome assay . The results<br />
confirm that in addition to its remarkable simplicity, the SOS Chromotest is a powerful method to<br />
detect <strong>and</strong> evaluate genotoxic agents<br />
462<br />
COOPERATIVE EFFECTS IN ASSAYS OF CHEMICAL MIXTURES OF ATMOSPHERIC POLLUTANTS .<br />
A .S . Raj <strong>and</strong> D .M . Logan . York University, North York, Ontario, Canada M3J 1P3<br />
Exposure to pollutants in natural atmospheres usually involves complex mixtures<br />
of chemicals rather than a single pollutant . In such cases risk assessment is<br />
difficult if not impossible because the chemicals may interact in several<br />
unpredictable ways . The object of this research is to measure chemical interactions<br />
in certain bioassaya <strong>and</strong> define quantitatively their cooperativity . Nine common<br />
atmospheric pollutants (4 promutagens, 1 direct acting mutagen <strong>and</strong> 4 non mutagens)<br />
have been tested alone <strong>and</strong> in combinations of two <strong>and</strong> three in the Ames <strong>and</strong> micronucleus<br />
assays . For each of the combinations a strictly additive dose response has<br />
been calculated <strong>and</strong> compared with the actual response . In the Ames assay most<br />
mixtures produce fewer revertants than predicted <strong>and</strong> this is not due to S9<br />
limitation . In cases where the predicted response is biphasic ag . BaP <strong>and</strong> DMBA due<br />
to different threshold dosages, the actual response is not biphasic but parallels<br />
that of the lower threshold chemical . In a few mixtures (three or more chemicals)<br />
inclusion of the direct acting mutagen 1-nitropyrene produces a highly synergietic<br />
response ie . more than 5 times the additive response . Weighting factors have been<br />
calculated for each chemical tested which can be used to predict the response of<br />
new mixtures of the chemicals . This approach should prove valuable in predicting<br />
the risk due to environmental pollutants .<br />
This research was supported by a grant from the Ontario Ministry of the Environment .<br />
http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />
1989 EMS Abstracts 159<br />
Notes