Spontaneous neoplasm incidences in Fischer 344 rats and B6C3F1 mice in two-year carcinogenicity studies:: A National Toxicology Program update

被引:204
作者
Haseman, JK [1 ]
Hailey, JR [1 ]
Morris, RW [1 ]
机构
[1] NIEHS, Biostat Branch, Res Triangle Pk, NC 27709 USA
关键词
tumor incidence; historical control data; F344; rats; B6C3F(1) mice; National Toxicology Program;
D O I
10.1177/019262339802600318
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Spontaneous neoplasm rates were determined for control Fischer 344 (F344) rats and B6C3F(1) mice from 2-yr rodent carcinogenicity studies carried out by the National Toxicology Program (NTP). The most frequently occurring neoplasms in untreated male F344 rats were testicular adenoma (89.1%), mononuclear cell leukemia (50.5%), adrenal gland pheochromocytoma (31.9%), and pituitary gland neoplasms (30.4%). For untreated female F344 rats, the most frequently occurring neoplasms were pituitary gland neoplasms (54.2%); mammary gland fibroadenoma (41.2%), and mononuclear cell leukemia (28.1%). The: most frequently occurring neoplasms in untreated male B6C3F, mice were liver adenoma/carcinoma (42.2%), lung adenoma/carcinoma (20.5%), and malignant lymphoma (8.3%). For untreated female B6C3F, mice, the most frequently occurring neoplasms were liver adenoma/carcinoma (23.6%), malignant lymphoma (20.9%), and pituitary gland adenoma/carcinoma (14.8%). The tumor rates observed in feeding study (untreated) and inhalation study (chamber) control rats were generally similar. The major exceptions were pituitary gland tumors and testicular adenoma in male F344 rats. The overall incidence of testicular adenoma was much lower in chamber controls (69.4%) than in feeding study controls (89.1%), whereas pituitary gland neoplasms showed the opposite trend (60.7% vs 30.4%). The most likely explanation for this difference is related to the individual housing of chamber controls and the group housing of feeding study controls. Differences in diagnostic criteria may influence reported tumor rates. To ensure consistency and comparability of tumor diagnosis from study to study, the NTP uses rigorous histopathology quality assurance and peer review procedures. Biological factors such as body weight may also affect tumor incidence. For example, increased body weights are associated with increased incidences of certain site-specific neoplasms, especially pituitary gland and mammary gland neoplasms in rats and liver tumors in mice. The presence of Helicobacter hepaticus has been associated with an increased incidence of liver neoplasms in male B6C3F, mice. Other factors that may produce differences in control tumor rates from study to study include diet, environmental factors, genetic drift, study duration, and survival differences. The NTP database provides historical control data that may be useful in the evaluation of possible chemically related changes in tumor incidence. However, it is essential that the study being evaluated be comparable to those in the NTP database with respect to those factors that are known to influence tumor occurrence.
引用
收藏
页码:428 / 441
页数:14
相关论文
共 46 条
  • [1] The sensitivity of the NTP bioassay for carcinogen hazard evaluation can be modulated by dietary restriction
    Abdo, KM
    Kari, FW
    [J]. EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 1996, 48 (2-3) : 129 - 137
  • [2] FDA points-to-consider documents: The need for dietary control for the reduction of experimental variability within animal assays and the use of dietary restriction to achieve dietary control
    Allaben, WT
    Turturro, A
    Leakey, JEA
    Seng, JE
    Hart, RW
    [J]. TOXICOLOGIC PATHOLOGY, 1996, 24 (06) : 776 - 781
  • [3] [Anonymous], [No title captured]
  • [4] [Anonymous], 1985, HDB CARCINOGEN TESTI
  • [5] BOORMAN GA, 1986, MANAGING CONDUCT DAT, P271
  • [6] SPONTANEOUS NEOPLASMS IN B6C3F1 MICE
    CHANDRA, M
    FRITH, CH
    [J]. TOXICOLOGY LETTERS, 1992, 60 (01) : 91 - 98
  • [7] Chemicals associated with decreases in the incidence of mononuclear cell leukemia in the Fischer rat
    Elwell, MR
    Dunnick, JK
    Hailey, JR
    Haseman, JK
    [J]. TOXICOLOGIC PATHOLOGY, 1996, 24 (02) : 238 - 245
  • [8] GART J, 1986, SCI PUBLICATION INT, V79
  • [9] GART JJ, 1979, J NATL CANCER I, V62, P957
  • [10] NEOPLASTIC AND NONNEOPLASTIC LESIONS IN AGING F344 RATS
    GOODMAN, DG
    WARD, JM
    SQUIRE, RA
    CHU, KC
    LINHART, MS
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1979, 48 (02) : 237 - 248