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Enhanced Deoxyribonuclease Activity in Human Transformed Cells and in Bloom's Syndrome Cells

โœ Scribed by Mauro Mezzina; Silvano Nocentini; Jeannette Nardelli; Georges Renault; Ethel Moustacchi; Alain Sarasin


Book ID
102944228
Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
568 KB
Volume
2
Category
Article
ISSN
0899-1987

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โœฆ Synopsis


Human hereditary diseases such as xeroderma pigmentosum, Fanconi's anemia, ataxia telangiectasia, and Bloom's syndrome are characterized by a proneness for developing cancer associated with abnormalities in the processing of DNA damage. The molecular defects responsible for predisposing human tissues t o cancer are still not well understood, despite the fact that a considerable amount o f work has already been done on this problem. In this paper, w e show that in human tumor cell lines, in cells transformed by DNA tumor viruses, and in cells derived from certain cancer-prone disorders, the level of activity o f a 42-kDa deoxyribonuclease is many times higher than in diploid untransformed control cells. This suggests that this activity is linked to, or may play a role in, malignant transformation.


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