Document 3e7v7N02JDzg3OKn34MJ1GNeO

n CHEMICAL MANUFACTURERS ASSOCIATION AtC, August 30, *" *<> To: Vinyl Chloride Project Panel Vinyl Chloride Research Coordinators / Gentlemen: - .Jk'' Enclosed is your copy of the quarterly report describing research completed under the CMA agreement with the University of Louisville for the 1979 - 80 fiscal year. Under the research program entitled "Research Techniques;^ and Methods for Detection and Prevention of Carcinogenesis , in Industrial Workers", by Dr. Tamburro and his staff, progress^ : . ,is .reported for each component of this.overall program. , Sincerely, ' J. T. Seawell Project Administrator Vinyl Chloride Project JTStbj Enclosure 1825 Connecticut Avenue. NW Washington. DC 20009 Telephone 202/328-4200 Telex 89617 (CMA WSH) ucc 000346 UNIVERSITY OF LOUISVILLE LOUISVILLE, KENTUCKY 40232 SCHOOL OF MEDICINE DEPARTMENT OF MEDICINE DIGESTIVE DISEASES AND NUTRITION SECTION July 30, 1979 \ HEALTH SCIENCES CENTER WALNUT t PRESTON STREETS Mr. Joseph T. Seawall Program Manager Manufacturing Chemists Association 1825 Connecticut Avenue, N.W. Washington, D.C. 20009 I RE: Quarterly Report for the Manufacturing Chemists Association's Agreement with the University of Louisville for the 1979-80 Fiscal Year. Dear Mr. Seawall: The following described what has been completed during the past quarter of the Manufacturing Chemists Association's agreement with the University of Louisville entitled, "Research Techniques and Methods for Detection and Pre vention of Carcinogenesis in Industrial Workers". Progress for each technical proposal will be reported separately. Technical Proposal A -- Immunological Systems for the Detection of Vinyl Chloride and Other Chemical Injury. H. P. Fortwengler Fortwengler's laboratory has continued evaluating three Independent- aspects of the immune system of Industrial workers to determine whether cancer can be detected earlier or to identify those at . high risk. Part I. Evaluation of Immmocompetence- of Exposed to Vinyl Chloride^ Chronically The purpose of this study was to determine the lmmunocompetence of Individuals that have undergone prolonged exposure to VC monomer and have developed liver lesions which, in some Instances, are thought to presage the development of the cancer angiosarcoma. Inmiunologlcal assays that have demonstrated usefulness In Indicating Inmunodepression In cancer patients were used. These tests evaluated the immunocompatence of individuals with possible pre-malignant lesions or other liver disease as demonstrated by biopsy. A comparison of the employees with demonstrated disease versus those employees with no clinical or laboratory evidence of disease showed no Immunological difference between the two groups. A comparison of VC workers having high VC exposure (those with lifetime exposure above ucc 000347 Mr. Jos ph T. Seawell July 30, 1979 Page 2 the plant median VC exposure) with individuals having low exposure (below the plant median) demonstrated a slight pattern of immunodepresslon when lymphocytes were stimulated by PHA and Con-A. However, further evaluation of this data, even after additl nal immunological parameters were examined, indicated there is no statistical significance between the high and low exposure groups. We are putting together data for a publication that indicates that there is no residual immunological depression as a result of chronic exposure to increased levels of VC as determined by the standard battery of immunological tests. Part II. HLA Frequencies in V.C. Workers. The microdroplet lymphocyte cytotoxicity test has been used lii our laboratory to tissue type for 11 separate HLA-A antigens and 16 HLA-B antigens and their possible Increased association with angio sarcoma or other chemically-related diseases. An Increased number of tests have been completed: approximately 471 individuals from the Louisville vinyl chloride polymerization plant have had their lymphocytes Isolated and typed. Part III. A Search for Evidence of a VC-Induced Tumor Antigen. A comparison of the responses between vinyl chloride plant w rkers and normal non-chemical plant workers indicated that there were many people in the general population having reactivity to hepatic tissue antigens irrespective of whether these antigens were from liver angiosarcoma or normal liver. Non-tumor specific reactions of this type may be due to sensitization by "natural" means, injections of human or animal substances, transfusions, etc. Vinyl chloride workers were classified according to known VC exposure and tested for reactivity to reagents prepared from normal liver or angiosarcoma liver. Lymphocyte responses from all individuals tested having low VC exposure (below plant median exposure) were compared to responses from all individuals having high exposure. No quanti tative statistical differences were noted between the reactivities of the two groups. When viewed qualitatively, concomitant reactions by an individual's lymphocytes to both normal liver and angiosarcoma liver cannot be interpreted. Angiosarcoma reagent contains both normal and tumor antigen. Therefore, only those remaining individuals with reactions to either normal liver or angiosarcoma liver alone were compared further. The composition of that group of individuals reacting to the angiosarcoma liver reagent was striking--the only reactions ob tained against this tumor preparation were from individuals with high VC exposure. That la, the individuals reacting to the tumor antigen reagent were all from the high risk group. UCC 000348 Mr. Joseph T. Seawell July 30, 1979 Page 3 We have further determined that because of the small number of indi viduals reacting to angiosarcoma antigen,statistical validity of these results cannot be demonstrated. As a result, these data must be interpreted with caution. In addition to testing for evidence of reactions to an angiosarcoma antigen, we have found that the tumors contain increased amounts of a normally occurring antigen, coagulation Factor VIII. Factor VIII is a large protein, often called antihemophilic factor, which was demonstrated by Hoyer et al. to be found differentially in endothelial cells, platelets and megakaryocytes. We have found FVIII in endo thelial cells lining the lumens of arteries and veins in normal liver sectioa when stained with rabbit anti-Factor VIII and FITC-conjugated anti-rabbit IgG. Normal sinusoidal linings displayed scanty fluorescense. / Sections of angiosarcoma, however, demonstrated a strikingly In creased fluorescence which appeared lining enlarged sinusoids. The intensity and expanse of positive fluorescence seen in angiosarcoma tissue was never seen in sinusoids of normal liver. Control sections indicated that the fluorescence was due to a specific antibody t anti-Factor VIII. We, therefore, conclude that the cell which be comes neoplastic in hepatic angiosarcoma Is the sinusoidal endothelial cell rather than the sinusoidal Kupffer cell. Technical Proposal B -- Biochemical Enzymatic Systems for the Detection of Vinyl Chloride and Other Chemical Injury and Cancer Development in Industrial Workers. J. T. Du Various liver cell types (hepatocytes, Kupffer and endothelial cells) have been Isolated by enzyme digestion. The nonhepatocytes are being separated into Kupffer and endothelial cells by countercurrent elutrlation. Enzymatic studies of the detoxifying activities of the subcellular fractions of liver cells, both hepatocytic and mesenchymal, are In progress. Enzyme studies Include glutathione S-epoxide transferase (GEST), glutathione S-aralkyl transferase (GAST) end glutathione reductase (GH). In addition, mixed function oxidase (MFO), the microsomal enzyma responsible for oxidation of vinyl chloride, was also determined in Isolated hepatocytes and mesenchymal cells. The extent of contamination of hepatocytes In mesenchymal cell preparation was investigated by Van Berkel and Kostel's method (Biochemical Characteristics of Nonparenchymal Liver Cells In Kupffer Cells and Other Liver Sinusoidal Cells, p. 299-306, ed. Wlsse and Knook, Elsevier, North Holland Biochemical Press, 1977) and found not to be appreciable. The results showed that the mesen chymal cells had about half the GEST activity, 7Z the GAST activity, less than half the MFO activity and 73% the glutathione reductase as compared to that of the hepatocytes. This preliminary result supports our hypothesis that the reason the endothelial cells become tumorous rather than hepatocytes is that the endothelial cells do not have the ability (or have an Impaired ability) to detoxify vinyl chloride meta bolites. Further experiments using Isolated endothelial cells and labelled vinyl chloride metabolite can provide more definitive answers ucc 000349 Mr. Joseph T. Seawell July 30, 1979 Page 4 Technical Proposal C -- Glycosaminoglycan Changes in Earlier Detection of Fibrotic Injury and Hepatic Cancer. C. E. Kupchella The:objeCtive of this proposal is.to determine the usefulness of urinary and tissue glycosaminoglycan measurements in the detection of chemically-induced liver injury. A summary of the pertinent results follows: 1. Human hepatic angiosarcoma and fibrotic liver diseases are accompanied by elevated tissue GAGs. The GAGs in the angio sarcoma tumor tissue are different from those in fibrotic tissue adjacent to the tumor. 2. Angiosarcoma and hepatoma patients have characteristic urinary GAG patterns -- patterns not found in normal controls. 3. Heparin sulfate (a type of GAG) is elevated in hepatic tissue undergoing experimentally-induced fibrosis and heparin sulfate is elevated la the urine or experimental animals. Also, heparin sulfate and hyaluronic acid'levels -- but not heparin -- ara 3-4 times higher in experimentally transplanted hepatomas than In normal liver and urinary excretion reflects both the tumor GAG composition and the size of tumors. 4. Livers of animals bearing metastasizing hepatoma (5123tc) have 10-fold greater concentrations of a non-sulfated, neutral, uronlc, add-positive material than is found in the livers f animals bearing two other, non-metastlsizlng hepatomas. 5. Hepatic necrosis is accompanied by significant tissue GAG ele vations, but hepatic regeneration Is not. Gross (non-fraetloned) urinary GAG determinations give a better indication of liver disease than ultrasound analysis. However, modifications in GAG analysis must be evaluated further as to specificity and sensitivity. 6. Exacting urinary GAG analysis (fractionated) la potentially able to differentiate active from Inactive liver disease. PRACTICAL SIGNIFICANCE: These studies address the needs for: a. Useful screening teats for liver Injury and for active versus Inactive disease -- urine tests of the type to be evaluated obviously fit the ideal of being non-invaslve and having zero norbldlty/mortallty and not requiring "time off". b. Methods of therapeutic Intervention, i.e., the elucidation of the role of the GAGs in the pathogenesis of fibrotic liver dis ease may well lead to the identification of strategies by which fibrogenesis can be blocked and/or reversed. ucc 000350 Mr. Joseph T. Seawell July 30, 1979 Page 5 Technical Proposal D -- Histological Systems of Detection. C. H. Tamburro, R. Schrodt Drs. Schrodt and Tamburro continue to develop a means of analyzing light microscopic sections of liver tissue obtained from vinyl chloride workers to determine the feasibility of quantitating the amount of scar tissue In these individuals related to their exposure. Sinusoidal cell size and collagen deposits within the sinus ldal Space of Disse have been determined by utilizing a relatively newly developed Hewlett-Packard 9864-A digitizer and a 9815-A micro com puter. With this equipment, Schrodt and Tamburro have been able to quantitate the areas of trichrome stainable collagen (fibrosis) within biopsy samples. These morphometric analyses have been done on randomly selected fields from biopsies obtained during medical evaluation in vinyl chloride workers. There are now some 110 biopsies approximately 50 of which have been reviewed. Morphometric analysis, however, has had to be delayed since there was no known standards of normal human collagen content known for human adults. A study has been begun to determine the normal distribution and con tent of collagen at varying ages in normal individuals without history of chemical, viral or medical disease or injury of the liver. This study is one-third complete. Preliminary review of the data suggests that there may be an increase in the collagen deposition (fibrosis), in the normal human liver associated with age. If this holds true upon analysis after completion of the study, age corrected standards will have been established so that the data obtained from the vinyl chloride exposed human biopsies.may be accurately interpreted. Resumption of the morphometric analysis of the vinyl chloride exposed liver biopsies will be resumed upon completion of the normal control study. Technical Proposal E -- Chemical Systems of Detection of Toxicity of Vinyl Chloride. J. L. Wong This study of vinyl chloride toxlcity/carclnogeniclty has been j: nceraed with (1) the chemistry of vinyl chloride metabolism, l.e., tMrlttkfRl of the Intermediates and their reactions with cytoplasmic cheetPnAW and (2) the putative actions of the primary metabolites on nuclear materials. The chemical reactions of two putative meta bolites, chlorooxixane (COR) and chloroacetaldehyde (CAA) with sulfhydryls (detoxification) as well as with nucleic acid constituents (mutagenesis and carcinogenesis) have been studied in detail. Part I. Detoxification Study. A previous attempt by Gothe et al. to trap the putative metabolites COR and CAA in vitro from vinyl chloride with 3,4-dichlorobenzenethi 1 has led to the identification of the product as 3,4-dichlorophenylthioacetaldehyde. It was Interpreted to be indicative of the formation of either COR or CAA. We have defined this experiment fur ther. Thus, chlorooxirane in organic medium reacts slowly with 3,4dichlorobenzenethiol to form 2-(3,4-dichlorophenylthio)acetaldehyde ucc 000351 Mr. Joseph T. Seawell July 30, 1979 Page 6 as 80% of the products. This reaction at room temperature takes about 7 days. At 60'C the reaction is completed in 21 hours giving the same products. (In both cases some disulfide Cl^Ph-S-S-Ph-C^ and other unidentified polymeric materials are observed.) The identity of the product was established by comparison of gas chroma* tography retention time with an authentic example, by PMR and by mass spectrum. In aqueous acetone (2:1) or aqueous acetonitrile (3:1), the reaction is much faster. As pH 4, 55% conversion la observed in 15 min. which is the lifetime of COR under these conditions, and 80% conversion at pH 7. The sole product identified from these reactions by high pressure liquid chromatography is the aldehyde indicated. On the other hand, chloroacetaldehyde in CHCl. gives another addition product, which was identified by PMR andJIR and its facile reversion to the starting materials as 3,4-Cl2ph-S-CH(OH) CH2C1 In aqueous acetone or aqueous acetonitrile, CAA did not react,witn the thiol within 1/2 hour, indicating its lower reactivity to the aromatic. SH group compared to COR. These results, combined with the in vitro experiment by Gotha, have confirmed that chlorooxlran is an obligatory intermediate in the metabolism of vinyl chloride. The detoxification of chlorooxirane was also studied in aqueous media at different pH's. K-Acetylcysteine was used as a typical cellular sulfydryl compound involved in detoxification. In aqueous solutions at pH4 and 7, their reaction was extremely fast at room temperature, yielding N-acetylcysteine-S-acetaldehyde. It was identified by ^ and C NMR and characterized as the 2,4-dintrophenylhydrazon. derivative. This aldehyde la probably the precursor of the urinary metabolites, S-2-hydroxyethylcysteine and thlbdiglycollc acid. Thus, the metabolic pathway of VC as shown below is strongly substantiated. CH2 - CH - Cl~ C" - OH - Cl RSH 9- RS - CH2 - CBO VC COR R - Ac-NH-CH-CHgCOOH Ae-NH-CH-C^-S-CHgCHg-OH + COOH Ac-NH-CH-CHj-S-C^-COOH . COOH L-y Ss((CcHh,2cooh)2 RSH - N-acetylcysteine, cysteine, glutathione Part II. Mutagenesis and Carcinogenesis Study. The detection study of the putative action of vinyl chloride is based on the hypothesis that such action comes from the modification of the nucleic acid materials by the primary metabolites COR and CAA. Although UCC 000352 Mr. Joseph T. Seawell July 30, 1979 Page 7 CAA is long known to react with nucleic acid-bases such as cytosine and adenine to form the etheno derivatives, little is known about the reaction of CAA on the most reactive base guanine. To continue our study on CAA with guanine base using analytical tools such as HPLC, GC-MS and FT-NMR, we have found that the guanosine reaction is enormously complicated. The reaction is very dependent on pH. At pH 6.5, the linear-ethenoguanosine is the immediate product which can further react with CAA. There were also at least 2 other minor products when the aqueous reaction was titrated accurately to pH 7.00 + 0.01. There was one major product which is the same as one of the two minor products found at pH 6.3. This new major product is tentatively identified as the guanosine H*--acetaldehyde, an intermediate to the etheno derivative. The question of how does this etheno modification of the nucleic acid bases bring about physicochemical changes is also examined. By using 13C FT-NMR with the special technique DIS (Deuterium Inductive Shifts) In the undecouple mode, the chemical shifts of etheno-bases, nucleo sides, and deoxynucleosides were, assigned and compared. Some signi ficant electronic changes in the nuclei have been detected. Part III. Significance Broadly speaking, this study will lead to early detection and preven tion of industrial cancers. Our chemical methodologies (synthesis, structure, and analysis), applied as an Integral part of the multi disciplinary approach, will elucidate specific molecular events in the effects of vinyl monomers on Industrial workers. This information will form a rational basis for safe use of chemicals and design of preventive measures. Our molecular studies- also provide the oppor tunity to develop useful marker(s) in the form of metabolites in the pathogenesis of chemical Injury. Technical Proposal F -- Assays for the Carcinogenic Potential of Industrial Chemicals Utilizing Prokarystlc and Eukaryotic Systems. U. N. Streips In this quarter, we have primarily concentrated on the publication of our results, using data derived from our studies under the* MCA contract. These publications include one paper by Barnes, Sonnenfeld, and Streips.on our new Interferon assay. Also, there are two book chapters: 1) Streips, Laumbach, and Yasbln "Bacterial Mutation Monitors for Active Metabolites of Chemical Carcinogens: Bacillus Subtills Assays for Mutation and DNA Repair" and (2) a chapter in a handbook for industrial physicians co-authored by Tamburro, Wong, and Streips, "Approaches to Occupational Cancer". This activity Is equally vital to oiir research programs since it establishes our laboratories as leaders in the field of chemical carcinogenesis. The MCA has been acknowledged in all these publi cations . UCC 000353 Mr. Joseph T. Seawall July 30, 1979 Page 8 Technical Proposal G -- Tissue Antigens and Antibodies in the Detection of Vinyl Chloride Injury. Enrique Espinosa During this quarter part of the time was spent in the preparation and presentation of papers and manuscripts and In the continuation of part of our experimental work. Part I. Papers. Three of our papers which were referred to in the previous report were presented during the first week of April in the 1979 FASEB meetings, Dallas, Texas and one paper was presented on May 7 at the annual meeting^of the American Federation for Clinical Research, Washington, D.C. During the second week of June, wepresented the results obtained in our studies on the properties of cultured hepatoma cells at the 1979 Annual Meeting of the Tissue Culture Association, Seattle, Washington. Part IX. Experimental Work. Further tests have been performed on the serum and liver antigens of the celL sheets and supernatant fluids of cultured hepatoma cells (PLC/PRF/5). The cell monolayers were assayed separately from cul ture supernates. Four day cultures in J. Alexander medium were shifted to serum-free medium containing innulin (lOO ng/ml). Then dally harvests for five additional days were pooled; cell morphology remained excellent. These supernates were clarified by centrifugation and concentrated by ultrafiltration. The cells were scrap d from the vessels into a small volume of water, homogenized and clarified. These concentrates were then tested by agarose double lmmun diffusion against standard antiserums which were fully absorbed with fetal bovine serum. Both preparations were found to contain serum albumin, fibrinogen, transferrin, alpha-1 antitrypsin and alpha-2 macroglobulln but not inminoglobulins. This system may thus be used for the study of biosynthesis of serum proteins by hepatoma. The constituent of normal liver, liver-specific F antigen, had disappeared. Technical Proposal I -- Vinyl Chloride Metabolism in. Isolated Liver Cells. Richard C. Peldhoff Sophisticated equipment for the preparation of Isolated rat liver cells was ordered between March and May, 1979. Two of the scientific suppliers have yet to fill the orders for various production reasons. The majority of the equipment is present and wd anticipate being operatl nal in September. During the interim start-up period, we have proceeded to prepare and characterize specific antisera which will be used in the project. Rabbits were lmminized over a 2-month period and are being bled at 2-3 week intervals. The antisera is being further purified by ammonium sulfate precipitation and by ion-exchange chromatography. A quantitative "rocket" Immunoelectrophoresis assay has been set up to ucc 000354 Mr. Joseph T. Seawell July 30, 1979 Page 9 __ measure the antigen in nanogram quantities. Radioactive vinyl chloride metabolites will be incubated with isolated liver cells and the uptake. Intracellular transport and metabolism by various membrane and cytosol fractions will be investigated. This completes the quarterly report from the University of Louisvill Chemical Monomer Research Group. If there is need for further information or clarification, please do not hesitate to contact me. Sincerely yours. CHT:nlh KOVi-O Carlo H. Tamburro, M.D. Professor of Medicine Chief, Division of Digestive Diseases and Nutrition ucc 000355