TitleDifferential modulation of dibenzo[def,p]chrysene transplacental carcinogenesis: maternal diets rich in indole-3-carbinol versus sulforaphane.
Publication TypeJournal Article
Year of Publication2013
AuthorsShorey, LE, Madeen, EP, Atwell, LL, Ho, E, Löhr, CV, Pereira, CB, Dashwood, RH, Williams, DE
JournalToxicol Appl Pharmacol
Volume270
Issue1
Pagination60-9
Date Published2013 Jul 01
ISSN1096-0333
KeywordsAnimals, Anticarcinogenic Agents, Benzopyrenes, Carcinogens, Diet, Female, Indoles, Isothiocyanates, Lung Neoplasms, Male, Maternal Nutritional Physiological Phenomena, Maternal-Fetal Exchange, Mice, Mice, 129 Strain, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, Pregnancy, Thiocyanates
Abstract

Cruciferous vegetable components have been documented to exhibit anticancer properties. Targets of action span multiple mechanisms deregulated during cancer progression, ranging from altered carcinogen metabolism to the restoration of epigenetic machinery. Furthermore, the developing fetus is highly susceptible to changes in nutritional status and to environmental toxicants. Thus, we have exploited a mouse model of transplacental carcinogenesis to assess the impact of maternal dietary supplementation on cancer risk in offspring. In this study, transplacental and lactational exposure to a maternal dose of 15mg/Kg B.W. of dibenzo[def,p]chrysene (DBC) resulted in significant morbidity of offspring due to an aggressive T-cell lymphoblastic lymphoma. As in previous studies, indole-3-carbinol (I3C, feed to the dam at 100, 500 or 1000ppm), derived from cruciferous vegetables, dose-dependently reduced lung tumor multiplicity and also increased offspring survival. Brussels sprout and broccoli sprout powders, selected for their relative abundance of I3C and the bioactive component sulforaphane (SFN), respectively, surprisingly enhanced DBC-induced morbidity and tumorigenesis when incorporated into the maternal diet at 10% wt/wt. Purified SFN, incorporated in the maternal diet at 400ppm, also decreased the latency of DBC-dependent morbidity. Interestingly, I3C abrogated the effect of SFN when the two purified compounds were administered in equimolar combination (500ppm I3C and 600ppm SFN). SFN metabolites measured in the plasma of neonates positively correlated with exposure levels via the maternal diet but not with offspring mortality. These findings provide justification for further study of the safety and bioactivity of cruciferous vegetable phytochemicals at supplemental concentrations during the perinatal period.

DOI10.1016/j.taap.2013.02.016
Alternate JournalToxicol. Appl. Pharmacol.
PubMed ID23566957
PubMed Central IDPMC3999518
Grant ListP01 CA090890 / CA / NCI NIH HHS / United States
P30 ES00210 / ES / NIEHS NIH HHS / United States
P01 CA90890 / CA / NCI NIH HHS / United States
T32 ES07060 / ES / NIEHS NIH HHS / United States
T35 ES007316 / ES / NIEHS NIH HHS / United States
P42 ES016465 / ES / NIEHS NIH HHS / United States
T32 ES007060 / ES / NIEHS NIH HHS / United States
P30 ES000210 / ES / NIEHS NIH HHS / United States