Pulsed Electromagnetic Field Enhances Caffeic Acid
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Posted On: 06/13/2024 12:07:53 PM
Pulsed Electromagnetic Field Enhances Caffeic Acid Phenethyl Ester-induced Death of MCF-7 Breast Cancer Cells, . 2024 Jun
(PEMF used in conjunction with other therapies continues to expand its potential, in this Study it made a chemotherapy drug more efficient at killing cancer cells)
Abstract
Background/aim: Caffeic acid phenethyl ester (CAPE) exerts anticancer effects against several cancer types, including breast cancer. Pulsed electromagnetic field (PEMF) improves the efficiency of some chemotherapeutic drugs. In this study, we examined the effects of PEMF stimulation on the anticancer activity of CAPE in MCF-7 breast cancer cells and the underlying signal transduction pathways.
Conclusion : PEMF stimulation enhanced CAPE-induced cell death by activating p53, which regulates the expression of apoptosis-related molecules, subsequently activating the caspase-dependent apoptotic pathway in MCF-7 cells, suggesting that PEMF can be utilized as an adjuvant to enhance the effect of CAPE on breast cancer cells.
https://pubmed.ncbi.nlm.nih.gov/38821617/
(PEMF used in conjunction with other therapies continues to expand its potential, in this Study it made a chemotherapy drug more efficient at killing cancer cells)
Abstract
Background/aim: Caffeic acid phenethyl ester (CAPE) exerts anticancer effects against several cancer types, including breast cancer. Pulsed electromagnetic field (PEMF) improves the efficiency of some chemotherapeutic drugs. In this study, we examined the effects of PEMF stimulation on the anticancer activity of CAPE in MCF-7 breast cancer cells and the underlying signal transduction pathways.
Conclusion : PEMF stimulation enhanced CAPE-induced cell death by activating p53, which regulates the expression of apoptosis-related molecules, subsequently activating the caspase-dependent apoptotic pathway in MCF-7 cells, suggesting that PEMF can be utilized as an adjuvant to enhance the effect of CAPE on breast cancer cells.
https://pubmed.ncbi.nlm.nih.gov/38821617/
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