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Environmental and Molecular Mutagenesis - Legacy Tobacco ...

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495 - 1989 EMS Abstracts<br />

IONIZING RADIATION AND GENETIC RISKS : CURRENT STATUS NO `eS<br />

K . Sankaranarayanan, Daf'artment of Radiation Genetics <strong>and</strong> Chemical Hutagenesis,<br />

Sylvius Laboratories, State University of Leiden, Leiden, The Netherl<strong>and</strong>s<br />

Estimates of the risk of genetic disease in the progeny of parents or populations<br />

exposed to ionizing radiai>on are made on the basis of mutation data from animal<br />

experiments <strong>and</strong> using a number of assumptions to bridge the gap Tetween induced<br />

mutation <strong>and</strong> genetic disease in man . The natural prevalence of genetic <strong>and</strong> multifactorial<br />

diseases in the population provides not only a framework for risk perception,<br />

but also is used in the act¢ffl calculattde of risks .<br />

Current estimates of genetic risks relate primarily to expected increases in the<br />

frequencies of those diseases with Mendelian patterns of inheritance ; their natural<br />

prevalence is of the order of 1 .25% . However, for multifactorial diseases, whose<br />

natural life-time prevalence is well over 50%, no reliable estimates of risk can be<br />

made in view of the fact that the relationship between mutation <strong>and</strong> disease is not<br />

well-understood . Animal studies using multifactorial traits as indicators of genetic<br />

damage <strong>and</strong> the genetic studies of the Hiroshima <strong>and</strong> Nagasaki populations (in the latter<br />

two of the indicators used are multifactorial) have failed to demonstrate significant<br />

adverse effects as a result of radiation exposures . However, as is well-known,<br />

mutation studies with experimental mammals have provided good evidence for the induction<br />

of mutations . The possible reasons for these discrepancies will be briefly<br />

discussed . Additionally, the relevance of knowledge on the nature of spontaneous <strong>and</strong><br />

radiation-induced mutations in the context of risk estimation will be considered .<br />

496<br />

IMMUNOLOGIC METHONS FOR THE DETECTION OF CARCINOGEN ADDUCTS IN HUMANS<br />

R . M . Santella, Columbia University New York, NY<br />

Monoclonal ant,ibodies have been developed which recognize a number of<br />

carcinogen-DNA <strong>and</strong> protein adducts . These antibodies can be used in highly<br />

sensitive competitive enzyme linked immunosorbent assays (ELISA) to detect femtomole<br />

levels of adducts in human samples . With the most sensitive antibodies, DNK adducts<br />

in the range of 1/l0s nucleotides can be measured . In addition, antibodies to DNA<br />

adducts can be used to investigate localization of adducts in specific cell types .<br />

We have used antibodies recognizing the major edduct of benzo(a)pyrene (BP) to<br />

monitor adducts in lymphocyte DNA of foundry workers <strong>and</strong> smokers end nonsmokers .<br />

Adducts in lung tissue of cancer patients <strong>and</strong> placental tissue of smokers <strong>and</strong><br />

nonsmokers have also be analyzed . Because of antibody crossreactivity with<br />

structurally related adducts of other polycyclic aromatic hydrocarbons, this assay<br />

is not specific for BP adducts . Monoclonal antibodies against 8-methoxypsorelen-•DNA<br />

adducts have been used to monitor adducts in psoriasis patients treated with this<br />

chemotherapeutic agent . Immunofluoreacence staining of skin biopsies from patients<br />

demonstrated adduct localization to epidermal cells . Studies with antibodies to<br />

aflatoxin-Ri-DNA adducts were used to detect elevated levels of adducts in liver<br />

tissue from Taiwanese hopatocellular cancer patients . Adduct detection in humans is<br />

now established as a viable method for determination of exposure to certain chemical<br />

carcinogens . The relationship of adduct. measurements to risk requires further<br />

investigation .<br />

497<br />

CYrOGEMETIC RISK ASSES9Etfr OF OPERATI011 T/EATRE PERSOI~EL<br />

S .T . SANIHIYA . V. Padsrani <strong>and</strong> A. Raassh. Departsant of Genetics . University of Madras, Madras - 600 113<br />

(India) . Occupational health risk to personnel working in operation theatres have been extensively<br />

studied . Although results are controversial . many agree that they constitute a potentially risk group <strong>and</strong><br />

needs to be periodically aonitored . This is particularly relevant, to countries,Yhere safety NasurN<br />

at work places receive less priority than desired . Therefore, the present work is contemplated to assess<br />

cytoyenetic risk on anaesthetists <strong>and</strong> supportive staff aeployed in a major referral hospital of Madras .<br />

The study group consisted of 16 snaasthetists <strong>and</strong> 4 theatre assistants serving for 1-33 years (13 .50 s<br />

7 .6) in several surgical theatres, which do not have any scavenging device . N40, ether <strong>and</strong> halothane are<br />

being used aither singly or in combination . Control group (n - 20) consisted of persons with different<br />

occupational set up . satched for possible confounding variablas . Cytopenetic damage !s assessad in terms<br />

of chroaososal aberrations (CA) <strong>and</strong> sister chromatid exchanges (SCE) observed !n 48 <strong>and</strong> 72h lysphocyte<br />

cultures of peripheral blood . Stp-rise regression analysis was performed taking duration of service (xl),<br />

ege (x )u sex (x3) <strong>and</strong> saokinp status (x4) as indep<strong>and</strong>ent variables <strong>and</strong> risk aeasures (f setaphuas with<br />

<strong>and</strong> vi~hout gaps - CA (G .) <strong>and</strong> CA (G -) <strong>and</strong> SCE/cell) as dependent variables using SPSS . Only xl !s the<br />

significant determinant of the variation in CA . This accounted for 609 upvards of the variation . For<br />

SCE . both x) <strong>and</strong> x3 are significant detersinants. xl alone explained eef of the variation <strong>and</strong> both together<br />

accounted for about 915 of the variation !n SCE . 8ased on these findings, it is concluded that persons<br />

working in theatres devoid of scavenging measures are at potential risk of genetic damage which appears<br />

to increase with duration of service .<br />

analysis .<br />

Thanks to our Prof .P .M.Gopinath for encouragement <strong>and</strong> Dr .M .Laks)ranan . CMC. Vellore for Computer<br />

http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />

171

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