Expression of peroxisome proliferator activated receptor mRNA in normal and tumorigenic rodent mammary glands

被引:48
作者
Gimble, JM
Pighetti, GM
Lerner, MR
Wu, XY
Lightfoot, SA
Brackett, DJ
Darcy, K
Hollingsworth, AB
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Surg, Oklahoma City, OK 73190 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Cell Biol, Oklahoma City, OK 73190 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73190 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Inst Breast Hlth, Oklahoma City, OK 73190 USA
[5] Vet Affairs Med Ctr, Oklahoma City, OK 73104 USA
[6] Roswell Pk Canc Inst, Dept Expt Therapeut, Buffalo, NY 14263 USA
关键词
D O I
10.1006/bbrc.1998.9858
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peroxisome proliferator activated receptors (PPARs) alpha, beta/delta, and gamma are novel nuclear hormone receptors activated by long chain fatty acids and synthetic Ligands and which regulate lipid metabolism. Recent studies have detected PPAR gamma 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 alpha, beta/delta, and gamma mRNAs based on northern blot analysis. The PPAR gamma isoform was predominantly gamma 2 based on quantitative PCR analysis. During pregnancy and lactation, the PPAR alpha and gamma mRNAs decreased while the PPAR beta/delta mRNA remained relatively unchanged. NMuMG: cells, an epithelial Line derived from normal murine mammary gland, expressed PPAR alpha, beta/delta, and gamma mRNAs, independent of the presence or absence of compounds modifying PPAR activity. In rats, the physiologic expression pattern of PPAR gamma mRNA paralleled the murine model; levels were detected in virgin but not lactating mammary glands, In addition, the PPAR gamma 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. (C) 1998 Academic Press.
引用
收藏
页码:813 / 817
页数:5
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