developmental and lactational exposure to dieldrin alters mammary tumorigenesis in her2neu transgenic mice发展和授乳的接触狄氏剂改变her2neu转基因小鼠乳腺肿瘤发生.pdfVIP
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developmental and lactational exposure to dieldrin alters mammary tumorigenesis in her2neu transgenic mice发展和授乳的接触狄氏剂改变her2neu转基因小鼠乳腺肿瘤发生
Developmental and Lactational Exposure to Dieldrin
Alters Mammary Tumorigenesis in Her2/neu Transgenic
Mice
Heather L. Cameron*, Warren G. Foster
Department of Obstetrics and Gynecology, McMaster University, Hamilton, Ontario, Canada
Abstract
Breast cancer is the most common cancer in Western women and while its precise etiology is unknown, environmental
factors are thought to play a role. The organochlorine pesticide dieldrin is a persistent environmental toxicant thought to
increase the risk of breast cancer and reduce survival in the human population. The objective of this study was to define the
effect of developmental exposure to environmentally relevant concentrations of dieldrin, on mammary tumor development
in the offspring. Sexually mature FVB-MMTV/neu female mice were treated with vehicle (corn oil), or dieldrin (0.45, 2.25, and
4.5 mg/g body weight) daily by gavage for 5 days prior to mating and then once weekly throughout gestation and lactation
until weaning. Dieldrin concentrations were selected to produce serum levels representative of human background body
burdens, occupational exposure, and overt toxicity. Treatment had no effect on litter size, birth weight or the number of
pups surviving to weaning. The highest dose of dieldrin significantly increased the total tumor burden and the volume and
number of tumors found in the thoracic mammary glands. Increased mRNA and protein expression of the neurotrophin
BDNF and its receptor TrkB was increased in tumors from the offspring of dieldrin treated dams. This study indicates that
developmental exposure to the environmental contaminant dieldrin causes increased tumor burden in genetically
predisposed mice. Dieldrin exposure also altered the expression of BNDF and TrkB, novel modulators of cancer
pathogenesis.
Citation: Came
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