Hesperidin and Chlorogenic Acid Synergistically Inhibit the Growth of Breast Cancer Cells via Estrogen Receptor/Mitochondrial Pathway.
Pang-Hung HsuWei-Hsuan ChenChen Juan-LuShu-Chen HsiehShih-Chao LinRu-Tsun MaiShiow-Yi ChenPublished in: Life (Basel, Switzerland) (2021)
Breast cancer is the most common cancer in women worldwide. Hesperidin (Hes) and chlorogenic acid (CA) are traditional medicinal molecules that abundantly exist in natural plants or foods. These compounds have been shown to prevent and suppress various cancers and therefore can be utilized as adjunctive therapies to aid cancer treatment. Here, 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays show a greater synergistic inhibitory effect on the growth of breast cancer cells, MCF-7, but not normal breast cells, MCF-10A, than hesperidin or chlorogenic acid alone. We present the possible molecular signaling pathways in MCF-7 cells with or without herbal molecule treatments via proteomic approaches. The data were further analyzed by Ingenuity Pathway Analysis (IPA) and confirmed by quantifying mRNA associated with the estrogen-receptor signaling pathway and mitochondrial functions. We demonstrated that the expression of CYC1, TFAM, ATP5PB, mtATP6, mtDNA, and NRF-1 were decreased upon 12 h treatment, and subsequent ATP production was also significantly decreased at 24 h. These results identified a synergistic effect induced by combinational treatment with hesperidin and chlorogenic acid, which can regulate mitochondria and ATP production through the estrogen receptor pathway in MCF-7 cells. However, none of the treatments induced the generation of reactive oxygen species (ROS), suggesting that ROS likely plays no role in the observed pharmacological activities. Overall, our study sheds light on the adequacy of hesperidin and chlorogenic acid to serve as an adjunctive therapy when co-administrated with chemotherapy drugs in breast cancer patients.
Keyphrases
- estrogen receptor
- breast cancer cells
- induced apoptosis
- signaling pathway
- reactive oxygen species
- cell cycle arrest
- oxidative stress
- cell death
- pi k akt
- endoplasmic reticulum stress
- gene expression
- adipose tissue
- epithelial mesenchymal transition
- mesenchymal stem cells
- pregnant women
- risk assessment
- papillary thyroid
- binding protein
- machine learning
- metabolic syndrome
- poor prognosis
- high glucose
- dna methylation
- cell therapy
- mitochondrial dna
- locally advanced
- big data
- squamous cell carcinoma
- single molecule
- protein kinase
- lymph node metastasis
- label free
- artificial intelligence