Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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1989 EMS Abstracts<br />
.feronucl.us tast. Mo direct DNA darsiai capacity aas observed of tAs Organic Notes<br />
axtracts of strsst soil sa.plss from all eight dist:iets . AowesY . Mutagsoieiq<br />
aftsr rtatiolic acti .atien <strong>and</strong> ckro .osesn brsakia= effects wrs exhibited by<br />
orpnic oztraeta of street soil sasplos fro . industrial <strong>and</strong> oe.mreial areas<br />
from four districts . Q"otoxicity wws correlated with ttr prsssncs of<br />
bsnso(a)pyr .as .<br />
330<br />
ASBES'T06 PSSOCIATID III.IS=NP HESOTF>ELICNGi : GCNSISTLNP CFROMOG0t9iL QiF,NM IN 1S2Ctt<br />
CELL LIAES FROtd SIX PATIENIS .<br />
Lirviairiaa, K .I ., PalirrShlun3, K . Tanmilehto, L ., 1Mattson, K ., Jantunen, K ., Husgafvel-<br />
Pursiainen, K . Insti . of Occupational Health <strong>and</strong> 1 Univ . Hospital, Helsinki, FICIIAND<br />
Exposure to asbestos fibers is lanwri to be associated with malignant mesotheliema in<br />
at least 80% of the tumor cases . Karyotypic studies of m3sothelioma tissues have<br />
revealed a variety of changes involving different duomosares . A consistent kazyotypic<br />
abnormality oa :mon to niesotheliomas has not been reported previously . We have chracterized<br />
cytogenetically seven mesothelio:na cell lines <strong>and</strong> a short-term eulture whic3i have<br />
been established in our laboratory from ttsnor tissue or pleural fluid sanples fram six<br />
patients with pleural malignant mesothelioma . All the cases of our study have a heavy<br />
asbestos exposure history . Complex structural <strong>and</strong> ntmerical abnannalities were observed<br />
in all the cultures studied. Excess chromatid material of the short atm of diranosams 5<br />
was consistently seen in the cells of five patients . In four of the cases, monoea :y of<br />
c:lrcc,nsane 13 was observed . Additionally, double minute chrarosaees or harogeniously<br />
staining regions were frequently noted . The observed specific absormalities eottman to<br />
several patients, e .g . the excess of the p-ana of chrarosans 5 <strong>and</strong> monosony of chratrosare<br />
13 suggest the importanee of these karyotypic changes in the development of malignant<br />
nesotheliana . We have shawm that asbestos <strong>and</strong> glass fibers are able to induce ctu :anosanal<br />
damage in human primary mesothelial cell cultures in vitro . The possible association of<br />
these findings with the kaYyotypic changes in turor cells remains to be solved .<br />
331<br />
A STUDY ON THE WORKERS OF COKING PLANT WITH MICRONUCLEUS (MN) FREQUENCY .<br />
FRAGILE SITES (FRR .) AND SISTER CHROMATID EXCHRNGE (SCE)<br />
Liu Yongchang . Shanxi Cancer InstitutQ,Taiyuan .Shanxi (PRC)<br />
In this study, thrQa experiments had been done in coking workers <strong>and</strong><br />
in normal control .ThQy were divided into 5 groups according to different<br />
testing spots : 1 . Workers of coking workshop ; 2 . Other workars . 3 .Staffs<br />
who were not in the workshop . 4 . The individuals of the steel institute .<br />
S .Normal control :ThQ results were as follow : 1 .Ths :data of MN frQquancw<br />
in sequence were 3 .13. 3 .25, 2 .21 . 2 .10, 0 .44 : 2 . The sequence of<br />
chromosome aberration (CR) were 4 .13, 5 .05, 1 .50 . 2 .?2 . 0 .20 . 3 . The<br />
sequence of SCE were 9 .60. . 8 .58 . 8 .88' . 6 .32 . 6 .40 .ThQra were significant<br />
differences among all these data . The concentration of Bap detected at<br />
this 5 spots list as logarithmic valua* 2 .38, 1 .78 . 1 .00 . 0 .59 . E .41,<br />
respectivnlu . Compared these data with MN . CA <strong>and</strong> SCE by means of<br />
correlation tast- the results showed that all were positive correlations<br />
TharQ were 251 fra. at all . 60% in the chromosome group A <strong>and</strong> 22X in<br />
group B . Of the 113 identified fra . . 34 .5X were inheritable (3p14) <strong>and</strong><br />
47 .78% were corresponding to the nonr<strong>and</strong>om carcinoma fra . .<br />
332<br />
CHROMATIN ALTERATIONS DURING EXCISION REPAIR<br />
M. Ljungman <strong>and</strong> G . Ahnstrbm, Department of Radiobiology, Arrheniua Laboratories for Natural Sdeneea,<br />
University of Stockholm, S-10961 Stockbolm,Sweden .<br />
DNA excision repair in mammalian cells scema to be associated with chromatin modification events . Cells<br />
exposed to ultraviolet light appear to undergo a general type of chromatin modification while methylmethane<br />
sulphonate treatment induce a more localized modification . It has been our Intention to further investigate the<br />
mechanismc of these chromatinmodityingeventsinmammalian ceDa .Inapreviousttudy, kinedaofrepairinduced<br />
DNA str<strong>and</strong> breaks were followed in Y79 hamster cell cultures treated with methylmethana aulphonate (Id1vIS) .<br />
The shapes of the DNA str<strong>and</strong> break curves when adding the drug 3-aminobenramide suggest that poly(ADPriboso)polymerase<br />
was involved in locally modifjdog the chromatin prior to the rejoining step . Thia modification<br />
might be required in order for the ligase to gain access to the repair site. To study ehromatin alterations associated<br />
with nucleotide excision repair in human fibroblasts, we used the DNA-damagiog agents bleomycin, gamma<br />
radiation <strong>and</strong>8-methoxypsoralen .Ithasbeenshownthatthese agents react preferentiallywith DNA in open regions<br />
of the chromatin. Thus, they are suitable for talnng'snapahots' of the chromatin, revealing how open its structure<br />
is at any particular time . Results obtained on cells undergoing repair after UV-'uradution indicate that the<br />
http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />
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