Mezzina M, Nocentini S, Nardelli J, Renault G, Moustacchi E, Sarasin A
Laboratory of Molecular Genetics, Institut de Recherches Scientifiques sur le Cancer Villejuif, France.
Mol Carcinog. 1989;2(4):179-83. doi: 10.1002/mc.2940020402.
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 to cancer are still not well understood, despite the fact that a considerable amount of work has already been done on this problem. In this paper, we 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 of 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.
人类遗传性疾病,如着色性干皮病、范可尼贫血、共济失调毛细血管扩张症和布卢姆综合征,其特征是易于发生与DNA损伤处理异常相关的癌症。尽管已经在这个问题上做了大量工作,但导致人类组织易患癌症的分子缺陷仍未得到很好的理解。在本文中,我们表明,在人类肿瘤细胞系、由DNA肿瘤病毒转化的细胞以及源自某些易患癌症疾病的细胞中,一种42 kDa脱氧核糖核酸酶的活性水平比二倍体未转化对照细胞高许多倍。这表明这种活性与恶性转化有关,或者可能在恶性转化中起作用。