TY - JOUR
T1 - Expression of peroxisome proliferator activated receptor mRNA in normal and tumorigenic rodent mammary glands
AU - Gimble, Jeffrey M.
AU - Pighetti, Gina M.
AU - Lerner, Megan R.
AU - Wu, Xiying
AU - Lightfoot, Stan A.
AU - Brackett, Daniel J.
AU - Darcy, Kathleen
AU - Hollingsworth, Alan B.
N1 - Funding Information:
1This work was supported by IDEA grant RP950166 from the Department of Defense Breast Cancer Initiative, the University of Oklahoma Breast Health Research Endowment Fund, and the Department of Veterans Affairs Medical Research Service.
PY - 1998/12/30
Y1 - 1998/12/30
N2 - The peroxisome proliferator activated receptors (PPARs) α, β/δ, and γ are novel nuclear hormone receptors activated by long chain fatty acids and synthetic ligands and which regulate lipid metabolism. Recent studies have detected PPARγ mRNA in human mammary tumor cell lines. The current study examined the expression profile of PPAR mRNAs in normal and malignant rodent mammary tissues. Virgin murine mammary glands contained PPAR α, β/δ, and γ mRNAs based on northern blot analysis. The PPARγ isoform was predominantly γ2 based on quantitative PCR analysis. During pregnancy and lactation, the PPARα and γ mRNAs decreased while the PPAR β/δ mRNA remained relatively unchanged. NMuMG cells, an epithelial line derived from normal murine mammary gland, expressed PPAR α, β/δ, and γ mRNAs, independent of the presence or absence of compounds modifying PPAR activity. In rats, the physiologic expression pattern of PPARγ mRNA paralleled the murine model; levels were detected in virgin but not lactating mammary glands. In addition, the PPARγ mRNA was not detected in several histologically distinct 7,12-dimethylbenz(a)anthracene induced mammary tumors. These findings suggest that PPARs may regulate mammary epithelial and stromal cell function in response to physiologic or pathologic stimuli that profoundly alter lipid metabolism.
AB - The peroxisome proliferator activated receptors (PPARs) α, β/δ, and γ are novel nuclear hormone receptors activated by long chain fatty acids and synthetic ligands and which regulate lipid metabolism. Recent studies have detected PPARγ mRNA in human mammary tumor cell lines. The current study examined the expression profile of PPAR mRNAs in normal and malignant rodent mammary tissues. Virgin murine mammary glands contained PPAR α, β/δ, and γ mRNAs based on northern blot analysis. The PPARγ isoform was predominantly γ2 based on quantitative PCR analysis. During pregnancy and lactation, the PPARα and γ mRNAs decreased while the PPAR β/δ mRNA remained relatively unchanged. NMuMG cells, an epithelial line derived from normal murine mammary gland, expressed PPAR α, β/δ, and γ mRNAs, independent of the presence or absence of compounds modifying PPAR activity. In rats, the physiologic expression pattern of PPARγ mRNA paralleled the murine model; levels were detected in virgin but not lactating mammary glands. In addition, the PPARγ mRNA was not detected in several histologically distinct 7,12-dimethylbenz(a)anthracene induced mammary tumors. These findings suggest that PPARs may regulate mammary epithelial and stromal cell function in response to physiologic or pathologic stimuli that profoundly alter lipid metabolism.
UR - http://www.scopus.com/inward/record.url?scp=0032583608&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1998.9858
DO - 10.1006/bbrc.1998.9858
M3 - Article
C2 - 9918810
AN - SCOPUS:0032583608
SN - 0006-291X
VL - 253
SP - 813
EP - 817
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -