Chromosomal instability in amniocytes from fetuses of mothers who smoke

JAMA

Volumn 293, Issue 10, 2005, Pages 1212-1222

  De La Chica, Rosa Ana ^a   Ribas, Isabel ^b   Giraldo, Jesús ^a   Egozcue, Josep ^a   Fuster, Carme ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b Centro de Patologia Celular   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; ARTICLE; CHROMOSOMAL INSTABILITY; CHROMOSOME 11Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CONTROLLED STUDY; FEMALE; FETUS; GENOTOXICITY; HEMATOPOIESIS; HUMAN; LEUKEMOGENESIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SMOKING; STATISTICAL ANALYSIS; TOBACCO; AMNION FLUID; BLOOD DISEASE; CYTOLOGY; ENVIRONMENTAL EXPOSURE; MUTAGENESIS; PREGNANCY; PRENATAL EXPOSURE; PROSPECTIVE STUDY; RISK FACTOR;

ADULT; AMNIOCENTESIS; AMNIOTIC FLUID; CHROMOSOMAL INSTABILITY; CHROMOSOME BANDING; FEMALE; FETUS; HEMATOLOGIC NEOPLASMS; HUMANS; MATERNAL EXPOSURE; MUTAGENESIS; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; PROSPECTIVE STUDIES; RISK FACTORS; SMOKING;

EID: 14544280623     PISSN: 00987484     EISSN: None     Source Type: Journal    
DOI: 10.1001/jama.293.10.1212     Document Type: Article

References (35)

1. Vogler GP, Kozlowski LT. Differential influence of maternal smoking on infant birth weight: gene-environment interaction and targeted intervention. JAMA. 2002;287:241-242.
2. Ji BT, Shu XO, Linet MS, et al. Paternal cigarette smoking and the risk of childhood cancer among offspring of nonsmoking mothers. J Natl Cancer Inst. 1997;89:238-244.
3. Jalili T, Murthy GG, Schiestl RH. Cigarette smoke induces DNA deletions in the mouse embryo. Cancer Res. 1998;58:2633-2638.
4. Lackmann GM, Salzberger U, Tollner U, et al. Metabolites of a tobacco-specific carcinogen in urine from newborns. J Natl Cancer Inst. 1999;91:459-465.
5. Jauniaux E, Gulbis B, Acharya G, et al. Maternal tobacco exposure and cotinine levels in fetal fluids in the first half of pregnancy. Obstet Gynecol. 1999;93:25-29.
6. Milunsky A, Carmella SG, Ye M, et al. A tobacco-specific carcinogen in the fetus. Prenat Diagn. 2000;20:307-310.
7. Ban S, Cologne JB, Neriishi K. Effect of radiation and cigarette smoking on expression of FUdR-inducible common fragile sites in human peripheral lymphocytes. Mutat Res. 1995;334:197-203.
8. Pluth JM, Ramsey MJ, Tucker JD. Role of maternal exposures and newborn genotypes on newborn chromosome aberration frequencies. Mutat Res. 2000;465:101-111.
9. Rowland RE, Harding KM. Increased sister chromatid exchange in the peripheral blood lymphocytes of young women who smoke cigarettes. Hereditas. 1999;131:143-146.
10. Littlefield LG, Joiner EE. Analysis of chromosome aberrations in lymphocytes of long-term heavy smokers. Mutat Res. 1986;170:145-150.
11. Shulman LP, Elias S, Tharapel AT, et al. Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes. Am J Obstet Gynecol. 1991;165:1877-1880.
12. Salonen K, Lahdetie J. No effect of maternal smoking in early pregnancy observed on chromosome aberrations in chorionic villus samples. Mutat Res. 1993;298:285-289.
13. Liang KY, Zeger SL. Longitudinal data analysis using generalized linear models. Biometrika. 1986;73:13-22.
14. Bōhm U, Dahm PF, McAllister BF, et al. Identifying chromosomal fragile sites from individuals: a multinomial statistical model. Hum Genet. 1995;95:249-256.
15. Greenbaum IF, Fulton JK, White ED, et al. Minimum sample sizes for identifying chromosomal fragile sites from individuals: Monte Carlo estimation. Hum Genet. 1997;101:109-112.
16. Stokes ME, Davis CE, Koch GG. Categorical Data Analysis Using the SAS System. 2nd ed. Cary, NC: SAS Institute Inc; 2000.
17. Price PJ. Chromosome abnormalities in amniotic fluid cells in culture. Karyogram. 1988;14:10-11.
18. Kerber S, Held KR. Early genetic amniocentesis: 4 years' experience. Prenat Diagn. 1993;13:21-27.
19. Human Gene Mapping 11: London Conference (1991): Eleventh International Workshop on Human Gene Mapping: London, UK, August 18-22, 1991. Cytogenet Cell Genet. 1991;58:1-984.
20. Musthapa MS, Lohani M, Tiwari S, et al. Cytogenetic biomonitoring of Indian women cooking with biofuels: micronucleus and chromosomal aberration tests in peripheral blood lymphocytes. Environ Mol Mutagen. 2004;43:243-249.
21. Norppa H. Cytogenetic biomarkers. IARC Sci Publ. 2004:179-205.
22. Miguez L, Fuster C, Pérez MM, et al. Spontaneous chromosome fragility in chorionic villus cells. Early Hum Dev. 1991;26:93-99.
23. Caporossi D, Vernole P, Nicoletti B, et al. Characteristic chromosomal fragility of human embryonic cells exposed in vitro to aphidicolin. Hum Genet. 1995;96:269-274.
24. Stein CK, Glover TW, Palmer JL, et al. Direct correlation between FRA3B expression and cigarette smoking. Genes Chromosomes Cancer. 2002;34:333-340.
25. Spitz MR, Wei Q, Dong Q, et al. Genetic susceptibility to lung cancer: the role of DNA damage and repair. Cancer Epidemiol Biomarkers Prev. 2003;12:689-698.
26. Glover TW. Instability at chromosomal fragile sites. Recent Results Cancer Res. 1998;154:185-199.
27. Richards RI. Fragile and unstable chromosomes in cancer: causes and consequences. Trends Genet. 2001;17:339-345.
28. Anderson D, Zeiger E. Human monitoring. Environ Mol Mutagen. 1997;30:95-96.
29. Kolialexi A, Mavrou A, Tsenghi C, et al. Chromosome fragility and predisposition to childhood malignancies. Anticancer Res. 1998;18:2359-2364.
30. Sasco AJ, Vainio H. From in utero and childhood exposure to parental smoking to childhood cancer: a possible link and the need for action. Hum Exp Toxicol. 1999;18:192-201.
31. Chen CS, Sorensen PH, Domer PH, et al. Molecular rearrangements on chromosome 11q23 pre-dominate in infant acute lymphoblastic leukemia and are associated with specific biologic variables and poor outcome. Blood. 1993;81:2386-2393.
32. Pathology and genetics of tumours of haematopoietic and lymphoid tissues. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, eds. World Health Organization Classification of Tumors. Lyon, France: IARC Press; 2001:86.
33. Cox MC, Panetta P, Lo-Coco F, et al. Chromosomal aberration of the 11q23 locus in acute leukemia and frequency of MLL gene translocation: results in 378 adult patients. Am J Clin Pathol. 2004;122:298-306.
34. Hall GW. Childhood myeloid leukaemias. Best Pract Res Clin Haematol. 2001;14:573-591.
35. Ford AM, Ridge SA, Cabrera ME, et al. In utero rearrangements in the trithorax-related oncogene in infant leukaemias. Nature. 1993;363:358-360.