4.6 Article

Screening of Specific and Common Pathways in Breast Cancer Cell Lines MCF-7 and MDA-MB-231 Treated with Chlorophyllides Composites

期刊

MOLECULES
卷 27, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27123950

关键词

chlorophyllides; microarray-based detection; breast cancer; MCF-7; MDA-MB-231

资金

  1. Ministry of Science and Technology, Taiwan [MOST 107-2311-B-214-002, MOST 108-2311-B-214-001, MOST 109-2311-B-214-001, MOST 109-2622-B-214-001, MOST 110-2311-B-214-001, MOST 110-2320-B-214-003]

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The study found that chlorophyllides composites can modulate the expression of various genes in breast cancer cells, including those associated with the endocrine and nervous systems. These findings provide valuable information for further research and development of novel cancer therapies.
Our previous findings have shown that the chlorophyllides composites have anticancer activities to breast cancer cell lines (MCF-7 and MDA-MB-231). In the present study, microarray gene expression profiling was utilized to investigate the chlorophyllides anticancer mechanism on the breast cancer cells lines. Results showed that chlorophyllides composites induced upregulation of 43 and 56 differentially expressed genes (DEG) in MCF-7 and MDA-MB-231 cells, respectively. In both cell lines, chlorophyllides composites modulated the expression of annexin A4 (ANXA4), chemokine C-C motif receptor 1 (CCR1), stromal interaction molecule 2 (STIM2), ethanolamine kinase 1 (ETNK1) and member of RAS oncogene family (RAP2B). Further, the KEGG annotation revealed that chlorophyllides composites modulated DEGs that are associated with the endocrine system in MCF-7 cells and with the nervous system in MDA-MB-231 cells, respectively. The expression levels of 9 genes were validated by quantitative reverse transcription PCR (RT-qPCR). The expression of CCR1, STIM2, ETNK1, MAGl1 and TOP2A were upregulated in both chlorophyllides composites treated-MCF-7 and MDA-MB-231 cells. The different expression of NLRC5, SLC7A7 and PKN1 provided valuable information for future investigation and development of novel cancer therapy.

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