Title:Regulation of LDLR, Bcl-2 and FASN Expressions by Oxidized Low Density Lipoprotein in Estrogen Receptor Positive Breast Cancer Cells
VOLUME: 16 ISSUE: 2
Author(s):Auni A. Hamid, Siti Aminah Ahmed and Shahrul Hamid*
Affiliation:Oncological and Radiological Sciences Cluster, Advanced Medical and Dental Institute, Universiti Sains Malaysia, 13200 Bertam, Kepala Batas, Penang, Infectomic Cluster, Advanced Medical and Dental Institute, Universiti Sains Malaysia, 13200 Bertam, Kepala Batas, Penang, Oncological and Radiological Sciences Cluster, Advanced Medical and Dental Institute, Universiti Sains Malaysia, 13200 Bertam, Kepala Batas, Penang
Keywords:Oxidized low-density lipoprotein, LDLR, Bcl-2, breast cancer, thymoquinone, FASN, NFκB, VAMP4.
Abstract:Background: One of the extensively studied antineoplastic agent is Thymoquinone
(TQ). Recent studies show increased level of oxidized low density lipoprotein
(oxLDL) among cancer patients. However, how oxLDL is involved in cancer cell survival
and growth is poorly understood. The goals of this study were to determine the molecular
effects of oxLDL on breast cancer cell (MCF7) growth and how they are modulated by
thymoquinone.
Methods: A cytotoxicity assay was conducted to determine the IC50 value of TQ. MCF7
cells were exposed to oxLDL for 72 hours in culture, after which phase contrast images
were taken. The characteristics of oxLDL-laden MCF7 cells and native MCF7 cells with
TQ treatment were studied using proteomic and gene expression assays.
Results: Microscopic images showed that oxLDL-laden MCF7 cells were larger than native
MCF7 cells. Bright immunofluorescence staining indicated Bcl-2 expression in the
cytoplasm and nucleus of oxLDL-laden MCF7 cells. Expression of fatty acid synthase
(FASN) and LDL receptor (LDLR) was localized in the cytoplasm of oxLDL-laden MCF7
cells. Native MCF7 cells did not exhibit expression of these proteins. Further investigation
showed increased expression of NFκB, Bcl-2, and LDLR in oxLDL-laden MCF7 cells
compared to native MC7 cells. In contrast, FASN expression was lower in oxLDL-laden
MCF7 cells compared to native cells. This could be due to availability of extracellular
oxLDL and reduced de novo lipid synthesis. Relative gene expression analysis demonstrated
downregulation of the EGLN1 gene in oxLDL-laden MCF7 cells, which indicates
cell proliferation that is in line with higher expression in Bcl-2 and NFκB. Similarly, the
VAMP4 gene was downregulated, which may indicate the presence of mature granules in
oxLDL-laden MCF7 cells. Treatment with TQ inhibited expression of Bcl-2, LDLR and
FASN but induced VAMP4 gene expression.
Conclusion: Results of this study suggest that TQ modulates oxLDL-induced expression
of markers in breast cancer growth.
