Increased tumors but uncompromised fertility in the female descendants of mice exposed developmentally to diethylstilbestrol

被引:138
作者
Newbold, RR
Hanson, RB
Jefferson, WN
Bullock, BC
Haseman, J
McLachlan, JA
机构
[1] NIEHS, Dev Endocrinol Sect, Reprod Toxicol Grp, Toxicol Lab,Environm Toxicol Program, Res Triangle Pk, NC 27709 USA
[2] NIEHS, Biostat Branch, Environm Dis & Med Program, Res Triangle Pk, NC 27709 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Comparat Med, Winston Salem, NC 27103 USA
[4] Tulane Univ, Environm Endocrinol Lab, Tulane Xavier Ctr Bioenvironm Res, New Orleans, LA 70112 USA
[5] Tulane Univ, Dept Pharmacol, New Orleans, LA 70112 USA
关键词
D O I
10.1093/carcin/19.9.1655
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prenatal exposure to diethylstilbestrol (DES) has been associated with the subsequent development of reproductive tract abnormalities, including poor reproductive outcome and neoplasia, in experimental animals and humans. Experimental animal studies with chemical carcinogens have raised the possibility that adverse effects of DES may be transmitted to succeeding generations. To evaluate this possibility and to determine if there is a sensitive window of developmental exposure, outbred CD-I mice were treated with DES during three stages of development: group I was treated on days 9-16 of gestation (2.5, 5 or 10 mu g/kg maternal body wt), the time of major organogenesis; group II was treated once on day 18 of gestation (1000 mu g/kg maternal body wt) just prior to birth; group III was treated on days 1-5 of neonatal life (0.002 mu g/pup/day), Female mice (F1) in each group were raised to sexual maturity and bred to control males. As previously reported, fertility of the F1 DES-exposed females was decreased in all groups. Female offspring (DES lineage or F2) from these matings were raised to maturity and housed with control males for 20 weeks. The fertility of these DES lineage female mice was not affected by DES exposure of their 'grandmothers'. DES lineage mice were killed at 17-19 and 22-24 months of age. An increased incidence of malignant reproductive tract tumors, including uterine adenocarcinoma, was seen in DES lineage mice but not in corresponding controls; the range and prevalence of tumors increased with age. Because uterine adenocarcinomas were seen in all three DES groups, all developmental exposure periods were considered susceptible to the adverse effects of DES, These data suggest that the reduced fertility observed in the DES F1 female mice was not transmitted to their descendants; however, increased susceptibility to tumor formation is apparently transmitted to subsequent generations.
引用
收藏
页码:1655 / 1663
页数:9
相关论文
共 43 条
[1]  
Boyd J, 1996, CANCER-AM CANCER SOC, V77, P507, DOI 10.1002/(SICI)1097-0142(19960201)77:3<507::AID-CNCR12>3.0.CO
[2]  
2-8
[3]   DEVELOPMENTAL EFFECTS OF ENDOCRINE-DISRUPTING CHEMICALS IN WILDLIFE AND HUMANS [J].
COLBORN, T ;
SAAL, FSV ;
SOTO, AM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 101 (05) :378-384
[4]  
Colborn T., 1992, CHEM INDUCED ALTERAT
[5]  
Colborn T., 1996, OUR STOLEN FUTURE
[6]  
Couse JF, 1997, MOL CARCINOGEN, V19, P236, DOI 10.1002/(SICI)1098-2744(199708)19:4<236::AID-MC4>3.0.CO
[7]  
2-A
[8]   CYTOGENETIC ANALYSIS OF MURINE CELL-LINES FROM DIETHYLSTILBESTROL-INDUCED UTERINE ENDOMETRIAL ADENOCARCINOMAS [J].
ENDO, S ;
KODAMA, S ;
NEWBOLD, R ;
MCLACHLAN, J ;
BARRETT, JC .
CANCER GENETICS AND CYTOGENETICS, 1994, 74 (02) :99-103
[9]   INCIDENCE OF SPONTANEOUS NEOPLASTIC AND NONNEOPLASTIC LESIONS IN CHARLES RIVER CD-1(R) MICE VARIES WITH BREEDING ORIGIN [J].
ENGELHARDT, JA ;
GRIES, CL ;
LONG, GG .
TOXICOLOGIC PATHOLOGY, 1993, 21 (06) :538-541
[10]   ESTROGEN EFFECTS ON CHROMOSOME-NUMBER AND SISTER CHROMATID EXCHANGES IN UTERINE EPITHELIAL-CELLS AND KIDNEY-CELLS FROM NEONATAL MICE [J].
FORSBERG, JG .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1991, 11 (03) :135-146