Analysis of chromosome aberrations by FISH and Giemsa assays in lymphocytes of cancer patients undergoing whole-body irradiation: comparison of in vivo and in vitro irradiation

Abstract. Studies of the frequencies of chromosome exchange aberrations in peripheral lymphocytes provide useful Purpose : To study the cytogenetic eVects of fractionated radiobiodosimetric information (IAEA 1986, Darroudi therapy in peripheral blood lymphocytes of ve cancer patients. 2000). For individual dose estimation, a calibration In vitro experiments were performed in parallel using the same dose-response curve constructed for human lympho- patients undergoing protracted whole-body irradiGiemsa-stained preparations were used to score unstable ation at low doses before local radiotherapy at high aberrations following in vivo and in vitro exposure. dose. Results: A linear dose-response curve was determined for both dicentrics and translocations. The in vivo frequency of translocations was higher than for dicentrics. Dose-response curves Materials and methods generated for translocations following in vivo and in vitro irradiation yielded similar frequencies. In contrast, for dicentrics, in 2.1. Subjects vitro irradiation yielded a higher frequency when compared with data generated following in vivo exposure. The study was performed on ve patients aged Conclusions : For dose reconstruction purposes, translocations fre-23-70 years, one woman and four men, with quency seems to be a more adequate end-point than the scoring advanced cancers and distant metastases

НЕИММУННЫЙ ОТЁК ПЛОДА ПРИ ВНУТРИУТРОБНОЙ ИНФЕКЦИИ

Nonimmune hydrops fetalis (NIHF) may be due to congenital infections. This article examines the congenital infections associated with NIHF – parvovirus and syphilis. Particular attention is paid to data verification infection and specificity of morphological changes in the placenta.Внутриутробная инфекция может сопровождаться неиммунным отёком плода. В данной статье приводятся практические наблюдения случаев неиммунного отёка плода при парвовирусной инфекции и сифилисе. Особое внимание уделено верификации данных инфекций и специфичности морфологических изменений в плаценте

Intrauterine infections with nonimmune hydrops fetalis

Nonimmune hydrops fetalis (NIHF) may be due to congenital infections. This article examines the congenital infections associated with NIHF – parvovirus and syphilis. Particular attention is paid to data verification infection and specificity of morphological changes in the placenta

International study of factors affecting human chromosome translocations

Chromosome translocations in peripheral blood lymphocytes of normal, healthy humans increase with age, but the effects of gender, race, and cigarette smoking on background translocation yields have not been examined systematically. Further, the shape of the relationship between age and translocation frequency (TF) has not been definitively determined. We collected existing data from 16 laboratories in North America, Europe, and Asia on TFs measured in peripheral blood lymphocytes by fluorescence in situ hybridization whole chromosome painting among 1933 individuals. In Poisson regression models, age, ranging from newborns (cord blood) to 85 years, was strongly associated with TF and this relationship showed significant upward curvature at older ages versus a linear relationship (p < 0.001). Ever smokers had significantly higher TFs than non-smokers (rate ratio (RR) = 1.19, 95% confidence interval (CI), 1.09-1.30) and smoking modified the effect of age on TFs with a steeper age-related increase among ever smokers compared to non-smokers (p < 0.001). TFs did not differ by gender. Interpreting an independent effect of race was difficult owing to laboratory variation. Our study is three times larger than any pooled effort to date, confirming a suspected curvilinear relationship of TF with age. The significant effect of cigarette smoking has not been observed with previous pooled studies of TF in humans. Our data provide stable estimates of background TF by age, gender, race, and smoking status and suggest an acceleration of chromosome damage above age 60 and among those with a history of smoking cigarettes. © 2008 Elsevier B.V. All rights reserved