The induction of sister chromatid exchanges by dihydrodiols derived from 7,12-dimethylbenz[a]anthracene and 3-methylcholanthrene.

Abstract:

:The in vitro induction of sister chromatid exchanges (SCEs) in Chinese hamster ovary (CHO) cells by the polycyclic hydrocarbons, 7,12-dimethylbena[a]anthracene and 3-methylcholanthrene and some of the related dihydrodiols was investigated. Increased numbers of SCEs were seen in the chromosomes of cells exposed to non-K-region dihydrodiols. The most active compounds were the 3,4-dihydrodiol of 7,12-dimethylbenza[a]anthracene and the 7,8- and 9,10-dihydrodiols of 3-methylcholanthrene: the parent hydrocarbons and their corresponding K-region dihydrodiols were relatively less active. The results are consistent with others that suggest that the metabolic activation of both hydrocarbons proceeds through the conversion of non-K-region dihydrodiols into vicinal diol-epoxides.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Pal K,Grover PL,Sims P

doi

10.1016/s0304-3835(79)80075-0

keywords:

subject

Has Abstract

pub_date

1979-06-01 00:00:00

pages

45-9

issue

1

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(79)80075-0

journal_volume

7

pub_type

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