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1.
Clin Transl Oncol ; 17(7): 511-20, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25532485

ABSTRACT

INTRODUCTION: In the mammary gland, the involution that occurs when lactation ends is an important period for cancer development. We have previously demonstrated stromal-epithelium interactions evaluating conditioned medium of adipose tissue on breast epithelial metalloproteases activity (Creydt et al., Clin Transl Oncol 15:124-131, 2013). Here, we evaluated the effects of conditioned medium of breast epithelial mammary cells on stromal cells. MATERIALS AND METHODS: Conditioned medium from normal murine mammary gland cell line (NMuMG) and conditioned medium proteins were obtained. Then, they were evaluated on modulation of adipocyte differentiation, using 3T3-L1 cell line. RESULTS: We described, for the first time, that breast epithelial mammary cells could produce the enzyme galactose 3-O-sulfotransferase 2 (GAL3ST2). Importantly, GAL3ST2 is present in NMMuMG and two human breast cancer cell lines, and it is more strongly expressed in more metastatic tumors. When 3T3-L1 preadipocyte differentiation was triggered in the presence of conditioned medium from NMuMG or GAL3ST2, triglyceride accumulation was decreased by 40 % and C/EBPß expression by 80 % in adipocytes. In addition, the expression of FABP4 (aP2), another marker of adipocyte differentiation, was inhibited by 40 % in GAL3ST2-treated cells. CONCLUSIONS: Taken together, these results suggest that GAL3ST2 would interfere with normal differentiation of 3T3-L1 preadipocytes; raising the possibility that it may affect normal differentiation of stromal preadipocytes and be a link to tumor metastatic capacity.


Subject(s)
Adipocytes/metabolism , Adipogenesis , Mammary Glands, Animal/metabolism , Sulfotransferases/metabolism , Sulfurtransferases/metabolism , 3T3-L1 Cells , Adipocytes/cytology , Animals , CCAAT-Enhancer-Binding Protein-beta/metabolism , Cell Differentiation , Cell Line, Tumor , Fatty Acid-Binding Proteins/metabolism , Female , HEK293 Cells , Humans , MCF-7 Cells , Mammary Glands, Animal/cytology , Mice , NIH 3T3 Cells , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Triglycerides/metabolism
2.
Redox Rep ; 18(6): 210-8, 2013.
Article in English | MEDLINE | ID: mdl-24112955

ABSTRACT

OBJECTIVES: Oxidative stress plays critical roles in the pathogeneses of diabetes, hypertension, and atherosclerosis, but its effect on fat accumulation is still unclear. In this study, we analyzed the role of the well-known antioxidant and a glutathione (GSH) precursor N-acetylcysteine (NAC) in fat accumulation and the expression of obesity-associated proteins. METHODS: We studied the effects of 10 µM NAC on obesity-related protein expression in cultured 3T3-L1 preadipocytes, which are able to differentiate into mature adipocytes and accumulate lipids. RESULTS: NAC treatment inhibited fat accumulation and reduced the expression of obesity-related proteins, including monoamine oxidase A, heat shock protein 70 (HSP70), aminoacylase -1 (ACY-1), and transketolase. DISCUSSION: Our results suggest that the effects of NAC on triglycerides (Tgs) and protein expression are correlated. In support of this, we showed that NAC treatment affected both the Tg synthesis pathway and the expression levels of proteins implicated in human obesity.


Subject(s)
Acetylcysteine/pharmacology , Adipocytes/metabolism , Adipogenesis/drug effects , 3T3-L1 Cells , Adipocytes/drug effects , Amidohydrolases/biosynthesis , Animals , Cell Differentiation/physiology , Fatty Acid-Binding Proteins/biosynthesis , HSP72 Heat-Shock Proteins/biosynthesis , Mice , Monoamine Oxidase/biosynthesis , Oxidative Stress/drug effects , Transketolase/biosynthesis , Triglycerides/metabolism
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