FOLLOWUS
1.Department of Biochemistry, University of Madras, Guindy Campus, Chennai(600025), India
2.Cancer Biology Lab, Department of Nanoscience and Nanotechnology, Sathyabama Institute of Science and Technology, Chennai(600119), India
3.VRR Institute of Biomedical Science, Kattupakkam, Chennai(600056), India
Prof. Devaki Thiruvengadam, E-mail:devakit@yahoo.co.uk
纸质出版日期:2021-09-01,
网络出版日期:2020-06-22,
录用日期:2019-09-20
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Ashok Mari, Gopikrishnan Mani, Sirpu Natesh Nagabhishek, 等. Carvacrol Promotes Cell Cycle Arrest and Apoptosis through PI3K/AKT Signaling Pathway in MCF-7 Breast Cancer Cells[J]. Chinese Journal of Integrative Medicine, 2021,27(9):680-687.
Ashok Mari, Gopikrishnan Mani, Sirpu Natesh Nagabhishek, et al. Carvacrol Promotes Cell Cycle Arrest and Apoptosis through PI3K/AKT Signaling Pathway in MCF-7 Breast Cancer Cells[J]. Chinese Journal of Integrative Medicine, 2021,27(9):680-687.
Ashok Mari, Gopikrishnan Mani, Sirpu Natesh Nagabhishek, 等. Carvacrol Promotes Cell Cycle Arrest and Apoptosis through PI3K/AKT Signaling Pathway in MCF-7 Breast Cancer Cells[J]. Chinese Journal of Integrative Medicine, 2021,27(9):680-687. DOI: 10.1007/s11655-020-3193-5.
Ashok Mari, Gopikrishnan Mani, Sirpu Natesh Nagabhishek, et al. Carvacrol Promotes Cell Cycle Arrest and Apoptosis through PI3K/AKT Signaling Pathway in MCF-7 Breast Cancer Cells[J]. Chinese Journal of Integrative Medicine, 2021,27(9):680-687. DOI: 10.1007/s11655-020-3193-5.
Objective:
2
To examine the role of carvacrol in modulating PI3K/AKT signaling involved in human breast cancer pathogenesis using
in vitro
experimental model MCF-7 cells.
Methods:
2
MTT and lactate dehydrogenase assays were performed with cells treated with different doses of carvacrol (0–250 μmol/L) at different time points (24 and 48 h). The nuclear morphology was assessed in MCF-7 cells with propidium iodide (PI) and acridine orange/ethidium bromide (AO/EB) staining and analyzed by fluorescence microscopy. Events like cell cycle arrest and apoptosis were observed by flow cytometric analysis and expressions of p-Rb
cyclin D1
cyclin-dependent kinase 4 (CDK4)
CDK6
Bax
Bcl-2
PI3K/p-AKT were analyzed by immunoblot.
Results:
2
Carvacrol significantly reduced cell viability with the half maximal inhibitory concentration value of 200 μmol/L at 24 and 48 h (
P
<
0.05). importantly
there was a significant increase in the accumulation of the G
0
/G
1
phase upon treatment with carvacrol in MCF-7 cells (
P
<
0.05 or
P
<
0.01). A remarkable decrease in protein expressions of p-Rb
cyclin D1
CDK4 and CDK6 denoted cell cycle arrest (
P
<
0.05 or
P
<
0.01). In addition
carvacrol treatment significantly inhibited PI3K/p-AKT protein expressions leading to induction of apoptosis mediated by decreased Bcl2 and increased Bax protein expressions. Further
Annexin V/PI staining by FACS analysis
dual staining by AO/EB and PI staining studies suggested induction of apoptosis by carvacrol through PI3K/Akt signaling pathway in MCF-7 cells.
Conclusion:
2
Carvacrol significantly inhibited the breast cancer MCF-7 cell proliferation and induced apoptosis via suppressing PI3/AKT signaling pathway.
carvacrolbreast cancerproliferationapoptosisPI3K/AKT signaling pathway
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