C. Tanzarella
Nuclear Regulatory Commission
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Featured researches published by C. Tanzarella.
Mutation Research | 1989
Francesca Degrassi; Rosella De Salvia; C. Tanzarella; Fabrizio Palitti
The induction of chromosomal aberrations and sister-chromatid exchanges (SCE) was studied in human lymphocyte cultures treated with camptothecin (CM), an inhibitor of mammalian topoisomerase I. While no chromosome-type aberrations were found in G1-treated cells, instead there was a dose-dependent induction of chromatid-type aberrations. These types of chromosomal alteration were not induced during the treatment itself but during the S phase, as CM is not efficiently removed with the normal washing procedure after treatment.
Mutation Research | 1985
G. Obea; G. Palitti; C. Tanzarella; Francesca Degrassi; R. De Salvia
Restriction endonucleases (REs) are able to induce chromosomal aberrations in Chinese hamster ovary (CHO) cells. The G1 phase of the cell cycle seems to be especially sensitive for the induction of chromosomal aberrations by REs. The different capacities of REs to induce chromosomal aberrations are probably correlated with the number of recognition sites in the genome.
Mutation Research | 2012
F. Berardinelli; D. Nieri; A. Sgura; C. Tanzarella; Antonio Antoccia
Many and varied are the proposed mechanisms that lead to resistance to ionizing radiation treatment. Among them, an inverse relationship between telomere length and radioresistance has been recently advanced. Investigating such a relationship in TK6 lymphoblasts, we found that clones originating from cells survived to 4Gy of X-rays showed a significantly higher telomere length when compared with clones grown from untreated cells. The lengthening observed was not attributable to a radiation-induced increase in telomerase activity, as demonstrated by TRAP assay performed in the dose range of 1-10Gy. Given the evidence that TK6 whole population was characterized by heterogeneity in cellular mean telomere length and telomere loss, we tested the hypothesis that a process of selection may favour cells with longer telomeres (more radioresistant cells) following exposure to irradiation. In order to do this 15 independent TK6 clones were selected and characterized for telomere length and loss on the basis of q-FISH and flow-FISH analysis. Among the screened clones four characterized by long telomeres and four characterized by short telomeres were tested for their radiosensitivity by means of clonogenic assay. The results obtained showed that, in our experimental conditions (cellular model, radiation doses) no significant correlation was observed between radiosensitivity and mean telomere lengths, whereas a positive correlation was observed with respect to telomere loss. Overall, these results indicate that telomere loss and not mean telomere length plays a critical role in the phenomenon of radiosensitivity/radioresistance.
Mutation Research\/genetic Toxicology | 1984
F. Degrassi; G. Fabri; F. Palitti; A. Paoletti; R. Ricordy; C. Tanzarella
To evaluate the possible genetic consequences of the industrial exposure among the vulcanizers of a rubber plant we measured the in vivo levels of chromosomal aberrations and sister-chromatid exchanges in peripheral lymphocytes of 34 vulcanizers and in an adequate control population. The observed chromosomal aberration frequencies were 1.9 +/- 1.4 aberrations/100 cells in the exposed group and 2.1 +/- 1.5 aberrations/100 cells in the controls. No difference was found between the two groups for the mean value of sister-chromatid exchanges (5.2 +/- 1.3 in the exposed, 5.2 +/- 0.7 in the control group). Cigarette-smoking was clearly associated with increased sister-chromatid exchange frequencies both in the exposed and in the control groups, while chromosomal aberration frequencies were not correlated with smoking habits.
Mutation Research\/genetic Toxicology | 1995
Daniela Modesti; C. Tanzarella; Francesca Degrassi
Nitrilotriacetic acid (NTA), a chelating agent, was tested for its ability to induce chromosomal damage in Chinese hamster cells. The chemical was shown to exert a weak genotoxic activity increasing the frequency of micronuclei after prolonged treatments. The analysis of kinetochore containing-micronuclei showed that NTA prevailingly induces chromosomal aberrations as compared to chromosome loss in hamster cells. Furthermore, immunostaining with an alpha-tubulin antibody showed clear alterations in the interphase microtubule network of cells treated for 24 h with 3 mM NTA. The microtubule effects of the chemical may be partly responsible for its cytotoxic effects.
Mutagenesis | 1986
C. Tanzarella; R. De Salvia; Francesca Degrassi; F. Palitti; H.C. Andersson; K. Hansson; B.A. Kihlman
Mutagenesis | 1995
Antonio Antoccia; L. Chessa; R. Ricordy; C. Tanzarella
Mutation Research\/environmental Mutagenesis and Related Subjects | 1984
F. Palitti; Renata Cozzi; Mario Fiore; P. Mosesso; R. Ricordy; C. Tanzarella
Mutation Research | 1979
C. Tanzarella; A. Modesti; R. De Salvia; E. Vitagliano
Mutagenesis | 1996
A. Sgura; R. Meschini; Antonio Antoccia; F. Palitti; G. Obe; C. Tanzarella