MOZDARANI H. ON THE EFFECTS OF ARA-A AND ARA-C ON X-RAY INDUCED DNA LESIONS IN NORMAL HUMAN AND A-T CELLS: SIMILARITIES AND DIFFERENCES.. Med J Islam Repub Iran 1992; 6 (2) :123-127
URL:
http://mjiri.iums.ac.ir/article-1-1492-en.html
From the School of Medical Sciences, Tarbiat Modarres University, Tehran, Islamic Republic of Iran.
Abstract: (4167 Views)
A better understanding of the mechanism of chromosomal aberration
formation could be obtained by using DNA repair inhibitors. Immortalized
normal human (MRC 5 SVI) and ataxia telangiectasia ( AT 5 BIV A )
fibroblastic cell lines were treated with adenosine arabinoside (ara-A) and
cytosine arabinoside (ara-C), both potent inhibitors of DNA dsb repair,
alone or in combination with x-rays at G2 or S-phase of the cell cycle. The
length of G2-phase for both cell lines was determined by autoradiographic
labeling to be about 4.5-5 h. A similar result was obtained by scoring of
chromosomally damaged cells following treatment with ara-A or ara-C for
various time intervals before fixation. The results obtained in this study show
that in spite of many similarities between the action of ara-A and ara-C, e.g.,
inhibition of DNA synthesis cIastogenic effects at G2 and S-phase and also
lack of synergism as a possible consequence of these similarities, ara-A was
found to have a different effect on rejoining of x-ray induced DNA lesions
than that of ara-C. Ara-A caused inhibition of chromatid deletion rejoining,
interpreted as inhibition of rejoining of DNA dsb at all sampling times before
fixation, whereas ara-C showed a synergistic effect on radiation-induced
DNA lesions, resulting in an increased frequency of chromatid deletions.
Thus there appears that these inhibitors have different modes of action on
x-ray induced DNA lesions, which may suggest a peculiar and important
difference in the nature of these two nucIeosides.