INVOLVEMENT OF A NON-BAY-REGION DIOL-EPOXIDE IN THE FORMATION OF BENZ(A)ANTHRACENE-DNA ADDUCTS IN A RAT-LIVER MICROSOMAL SYSTEM

被引:23
作者
MACNICOLL, AD
COOPER, CS
RIBEIRO, O
GERVASI, PG
HEWER, A
WALSH, C
GROVER, PL
SIMS, P
机构
[1] Chester Beatty Research Institute, Institute of Cancer Research: Royal Cancer Hospital, London, SW3 6JB England, Fulham Road
关键词
D O I
10.1016/0006-291X(79)91548-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The metabolic activation of benz(a)anthracene was investigated by incubating [3H]-benz(a)anthracene with DNA, a NADPH-generating system and rat-liver microsomes. When hydrolysates of the DNA were chromatographed on Sephadex LH20 columns, three hydrocarbon-nucleoside adduct peaks were resolved and these were further examined using HPLC. One adduct probably results from the reaction of the non-bay-region diol-epoxide r-8,t-9-dihydroxy-t-10,11-oxy-8,9,10,11-tetrahydrobenz(a)anthracene (anti-BA-8,9-diol 10,11-oxide) with DNA. The other two adducts did not co-chromatograph with adducts formed from any of the four possible isomeric diolepoxides that can be formed in the 8,9,10,11-ring of benz(a)anthracene. © 1979.
引用
收藏
页码:490 / 497
页数:8
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