Gene Expression Profiling of Maslinic Acid-treated MCF-7 Breast Cancer Cells Using Nanostring nCounter Pancancer Pathway Panel

•This study provides a full insight into the underlying mechanism of anticancer properties of a pentacyclic triterpene, maslinic acid (MA) against breast cancer cell line MCF 7.•20 DEGs were identified after MA treatment, these DEGs are mainly involved in several pathways which are the Pathway of Ca...

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Veröffentlicht in:Gene 2025-01, Vol.935, p.149043, Article 149043
Hauptverfasser: Tan, Soon Yan, Foo, Chai Nien, Ng, Foong Leng, Tan, Chee Hong, Lim, Yang Mooi
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Sprache:eng
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Zusammenfassung:•This study provides a full insight into the underlying mechanism of anticancer properties of a pentacyclic triterpene, maslinic acid (MA) against breast cancer cell line MCF 7.•20 DEGs were identified after MA treatment, these DEGs are mainly involved in several pathways which are the Pathway of Cancer, Focal Adhesion-PI3K-mTOR Signalling Pathway, PI3K-Akt, and Ras Signalling Pathway.•MA might be able to induce apoptosis via UPR respond.•MA was found to regulate genesinvolve in histone modification and Aerobic glycolysis. Breast cancer remains a significant global health concern, impacting millions of women every year. Maslinic acid (MA), a pentacyclic triterpene has been found to exert promising anticancer effect in various cancers, including breast cancer, yet the underlying mechanisms remain unclear. This study aims to elucidate the anticancer properties of MA via gene expression profiles in breast cancer cells. Cytotoxicity assay results revealed that MCF-7 exerts the highest sensitivity after 72 h of MA treatment followed by T-47D and MDA-MB-231. MCF-7 were then selected for in-depth analysis using the Nanostring nCounter Pancancer Pathway Panel to analyze the differential expression of genes (DEGs). Across three time points (24, 48, and 72 h), 20 significant DEGs were identified, of which 5 were upregulated and 15 were downregulated. In silico analysis indicated that these DEGs were involved in Pathway of Cancer, Focal Adhesion-PI3K-mTOR Signaling Pathway, PI3K-Akt, and Ras Signaling Pathway. The regulation of these DEGs contributes to several cellular activities such as apoptosis, inhibition of cell proliferation, cell cycle and survival, reduction of glycolysis, angiogenesis, and DNA repair. Additionally, the unfolded protein response emerged as a noteworthy biological process in this study. This study unravels the molecular mechanisms underpinning the therapeutic potential of MA against breast cancer.
ISSN:0378-1119
1879-0038
1879-0038
DOI:10.1016/j.gene.2024.149043