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b HKOSgS015 41870 2 ENHANCED CELLULAR BINDING AND PENETRATION OF NUCLEIC ACIDS CAUSED BY CHEMICAL
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HKOSgS015
41870 2
ENHANCED CELLULAR BINDING AND PENETRATION OF NUCLEIC ACIDS
CAUSED BY CHEMICAL AND PHYSICAL CARCINOGERS E~D MUTAGENS
PROC AM ASSoc.CANcER RES 17(0): 8; 1976
KUBINSKI, H/ MORIN, NM, ZELDIN, PE/ WEIIIHOUSE, S, FOTI, M
MEETING ABSTRACT: THE INITIAL OBSERVATION THAT A CARCINOGENIC
CHEMICAL, 1,3-PROPANE SULTONE~ INCREASES BINDING AND
PENETRATION OF DNA AND RNA TO EHRLICH ASCITES TUMOR CELLS IN
VITRO PROMPTED A COMPARISON OF THE EFFECTS OF OTHER
CARCINOGENS AND MUTAGENS IN'THE PRESENT INVESTIGATION, OVER
30 CHEMICALS WERE TESTED.
FINDINGS: NUCLEIC ACID ATTACHMENT TO AND SUBSEQUENT
PENETRATION INTO BOTH EUKARYOTIC AND PROKARYOTIC CELLS WAS
SIGNIFICANTLY ENHANCED BY ALL ULTIMATE CARCINOGENS.
FORMATION OF ARTIFICIAL NUCLEOPROTEINS BY ADDITION OF: A
BASIC PROTEIN TO THE REACTION MIXTURE FURTHER INCREASED THE
BINDING.
!IONULTIMATE DERIVATIVES AND NONCARCINOGENIC AND NONMUTAGENIC
CCMF'OUNDS HAD NO EFFECT, BUT PRECARCINOGENS AND INTERMEDIATE
CARCINOGENIC FORMS WERE ACTIVATED BY RAT DR MOUSE LIVER
EXTRACTS.
DNA IRRADIATED WITH ULTRAVIOLET LIGHT REACTED WITH THE CELLS
IN A MANNER SIMILAR TO THAT OF UNIRRADIATED CONTROL.
IRRADIATION IN THE PRESENCE OF LYSOZYME, HOWEVER~ ENHANCED
CELLULAR BINDING MORE THAN 20°FOLD.
C~l-R 9B I]OHG 01057

HKOSgS016
41870
DISCUSSION: SUCH INCREASED ATTACHMENT AND PENETRATION OF
NUCLEIC ACIDS CAUSED BY CHEMICAL AND PHYSICAL CARCINOGENS
CAN PLAY ,'. ROLE DURING THE PROCESS OF TUMOR INDUCTION.
OBSERVATIONS REPORTED HERE MAY FORM A 3ASI$ FOR DEVELOPING
A SIMPLE AND REPRODUCIBLE TEST SYSTEM FOR SCREENING OF
CARCINOGENIC AND MUTAGENIC COMPOUNDS.
/VOS/
(PRESENTED AT THE 67TH ANNUAL ~ETIN6 OF THE ~RICAN
ASSOCIATION FOR CANCER RESEARCH AND THE ~TH ANNUAL MEETING
OF THE AMERICAN SOCIETY OF CLINICAL 0NCOLOGY, TORONTO,
CANAJ~A, MAY 4-8, 1976,)
U WISC, M~ISOR, WIS/
U WISC, MADISOR, WIS
MEETING ABSTRACT, BIOCHEMICAL STUDY A, GENETIC STUDY A,
IN VITRO STUDY A, R J~DIATION STUDY A/ CYTOCHEMICAL STUDY A,
MICE, RATS, CARCINOOENICITY TESTING A, CARCINOGENESIS
MECHANISMS A, CARCINOGENS BIOASSAY A, CHEMICAL CARCINOGENESIS,
PHYSICAL CARCINOGENS, SCREENING TEST A, NUCLEIC ACID BINDING As
D~IA BINDING, ~IA BINDING, PROTEIN BINDING, CHEMICAL
BINDING, LIVER CELLS A, CARCINOGENS ACTIVATION A, CARCINOGENS
ACTION MECHANISMS A, CARCINOGENS BIOLOGICAL ACTIVITY,
CARCINOGENS METABOLIC EFFECTS A, NUCLEOPROTEIN A,
CARCINOGENS POTENCY A, CARCINOGENS PROMOTERS A, CARCINOGENS
CYTOTOXIClTY A, CHEMICAL MUTAGENS, CELL CHANGES A/
EHRLICH ASCITES TUMOR CELLS, CARCINOGENS CHEMICAL PROPERTIES,
CARCINOGENS PHYSICAL PROPERTIES, NUCLEIC ACID
METABOLISM DISORDERS, NUCLEIC ACID ~J3NORMALITIESj LIVER CELL
CHANGES A, LIVER EXTRACTS A, CELL IRRADIATION A,
CIR 9E~ CDHG 0"1050

HK0595~t7
41870
TUMOR INDUCTION HI, LYSOZYME A, CELL DNA CHANGES A, CELL R~A
CHANGES A, CELL NUCLEIC ACID CHANGES A, CELL PROTEIN CHANGES,
CARCINOGENS BINDI:rG A//
ENGLISH LANGUAGE, MADISON WI£ RESIDENCE, USA RESXDENCE~
GRANTOR USPHS, CONFERENCE, TORONTO CANADA, AMER ASSN CANCER
RE$, AMER SOC CLINICAL ONCOLOGY, TEMPLE UNIV
C~TF~ 9B 130lql~ 01059
