The Expression Profile of the RANK/RANKL/OPG Pathway in Breast Cancer Stem Cells Isolated From Breast Cancer Cell Lines

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hassnaa H. Elgohary, Mohamed M. Kamal, Sherine Maher Rizk, Nadine W. Maurice
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引用次数: 0

Abstract

The RANK/RANKL/OPG signaling pathway plays a crucial role in breast cancer progression and metastasis. However, its expression patterns and potential implications in breast cancer stem cells remain poorly understood. This study aimed to characterize the expression profile of this pathway in breast cancer stem cells isolated from two distinct breast cancer cell lines: MDA-MB-231 and MCF-7. Mammospheres (MS), representing breast cancer stem cells, were generated using agar-coated 6 well tissue culture plates in suitable mammospheres culture conditions. Flow cytometric analysis showed enrichment of the CD44+/CD24 subpopulations in the mammospheres cultures, with MDA-MB-231 exhibiting a higher percentage compared to MCF-7. The isolated MS from both cell lines showed upregulation of stemness markers OCT4 and SOX2, with MS. MDA-MB-231 demonstrating higher expression levels. Analysis of the RANK/RANKL/OPG axis revealed differential expression patterns between the two cell lines. RANK expression was significantly upregulated in MS. MDA-MB-231 but not in MS. MCF-7. Interestingly, while OPG mRNA levels were elevated in mammospheres from both cell lines, secreted OPG protein levels were paradoxically reduced in the mammospheres conditioned media. Additionally, RUNX2, an osteoblastic marker, and a downstream target of RANK signaling, showed a decreased expression in both mammospheres compared to adherent cells. These findings suggest a complex, context-dependent regulation of the RANK/RANKL/OPG pathway in breast cancer stem cells, potentially contributing to the aggressive nature and metastatic propensity of triple-negative breast cancer. This study provides novel insights into the molecular characteristics of breast cancer stem cells and underscores the complexity of OPG/RANK/RANKL axis expression in them; a role yet to be fully elucidated.

RANK/RANKL/OPG信号通路在乳腺癌的进展和转移中起着至关重要的作用。然而,人们对其在乳腺癌干细胞中的表达模式和潜在影响仍知之甚少。本研究旨在描述从两种不同的乳腺癌细胞系中分离出来的乳腺癌干细胞中该通路的表达谱:MDA-MB-231和MCF-7。代表乳腺癌干细胞的乳腺球(MS)是在合适的乳腺球培养条件下使用琼脂涂层的 6 孔组织培养板生成的。流式细胞仪分析表明,CD44+/CD24-亚群在乳腺球培养物中富集,与MCF-7相比,MDA-MB-231表现出更高的百分比。从两种细胞系中分离出的MS都显示出干性标志物OCT4和SOX2的上调,其中MS.MDA-MB-231的表达水平更高。对RANK/RANKL/OPG轴的分析显示了两种细胞系之间不同的表达模式。RANK表达在MS.MDA-MB-231中的RANK表达明显上调,而在MS.MCF-7。有趣的是,虽然两种细胞系的乳腺球中 OPG mRNA 水平都升高了,但乳腺球条件培养基中分泌的 OPG 蛋白水平却降低了。此外,与粘附细胞相比,RUNX2(一种成骨标志物,也是 RANK 信号转导的下游靶标)在两种乳腺小球中的表达均有所下降。这些研究结果表明,乳腺癌干细胞中的RANK/RANKL/OPG通路具有复杂的环境依赖性调控,可能导致三阴性乳腺癌的侵袭性和转移倾向。这项研究为乳腺癌干细胞的分子特征提供了新的见解,并强调了OPG/RANK/RANKL轴在乳腺癌干细胞中表达的复杂性;这一作用尚有待全面阐明。
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来源期刊
Journal of cellular biochemistry
Journal of cellular biochemistry 生物-生化与分子生物学
CiteScore
9.90
自引率
0.00%
发文量
164
审稿时长
1 months
期刊介绍: The Journal of Cellular Biochemistry publishes descriptions of original research in which complex cellular, pathogenic, clinical, or animal model systems are studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches. Submission of papers reporting genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize parameters of biological control in a cellular context are encouraged. The areas covered include, but are not restricted to, conditions, agents, regulatory networks, or differentiation states that influence structure, cell cycle & growth control, structure-function relationships.
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