Promotion by polychlorinated biphenyls of lung and liver tumors in mice

Anderson, LM; Logsdon, D; Ruskie, S; Fox, SD; Issaq, HJ; Kovatch, RM; Riggs, CM

HERO ID

201385

Reference Type

Journal Article

Year

1994

Language

English

PMID

7955061

HERO ID 201385
In Press No
Year 1994
Title Promotion by polychlorinated biphenyls of lung and liver tumors in mice
Authors Anderson, LM; Logsdon, D; Ruskie, S; Fox, SD; Issaq, HJ; Kovatch, RM; Riggs, CM
Journal Carcinogenesis
Volume 15
Issue 10
Page Numbers 2245-2248
Abstract Polychlorinated biphenyls (PCB), which are tumor promoters, have been found in human tissues for decades. Their contribution to cancer risk may only now start to appear, due to long human cancer latency and the nature of tumor promotion. Epidemiological associations have been seen between PCB exposure or tissue content and cancer at several sites. In rodents, tumor promotion by PCBs has been little studied in tissues other than liver. Previously, in an experiment modeling infant carcinogen exposure following PCBs received in milk, lung and liver tumors, initiated neonatally in mice by the environmental nitrosamine N-nitrosodimethylamine (NDMA), were promoted by later treatment with Aroclor 1254. The present study was undertaken to confirm and characterize the effects of Aroclor 1254 on tumor number, latency, size and malignancy. Male Swiss mice were given NDMA on postnatal day 4 and Aroclor 1254 (250 mg/kg) on day 8, and killed at intervals. Eight PCB congeners were quantified in the carcasses. Incidences of mice with NDMA-initiated lung tumors at 28 weeks of age were increased 2.5-fold by PCBs. Multiplicities of lung tumors were enhanced four-fold by PCBs at 28 and 52 weeks. By 72 weeks tumor numbers were similar in the NDMA-only and NDMA-PCB groups. Liver tumors first occurred in significant numbers at 52 weeks and only in mice receiving both NDMA and PCBs. As for the lung, at 72 weeks the incidence was high in both the NDMA-only and NDMA-PCB groups. Sizes of tumors and liver carcinoma incidence were not altered by PCB treatment. Carcass analysis revealed a significant positive association between lung tumor numbers at 28 weeks and relative percentage of 2,2',4,4',5-pentachlorobiphenyl, with no other correlations. The results confirm that PCBs promote lung as well as liver tumors, by triggering the early appearance of latent initiated tumors otherwise presenting in old age.
Pmid 7955061
Wosid WOS:A1994PM73300028
Is Certified Translation No
Dupe Override No
Comments N1-OctAN-7955061N1-Anderson, L MLogsdon, DRuskie, SFox, S DIssaq, H JKovatch, R MRiggs, C MComparative StudyEnglandCarcinogenesisCarcinogenesis. 1994 Oct;15(10):2245-8.N1-engAD-Laboratory of Comparative Carcinogenesis, National Cancer Institute, Frederick Cancer Research and Development Center, Ft Detrick, MD 21702-1201.ID-92
Is Public Yes
Language Text English
Keyword Animals; Body Burden; Dimethylnitrosamine; Female; Liver Neoplasms, Experimental/*chemically induced; Lung Neoplasms/*chemically induced; Male; Mice; Mice, Inbred Strains; Polychlorinated Biphenyls/*toxicity
Is Qa No