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Combination of Biochanin A and Temozolomide Impairs Tumor Growth by Modulating Cell Metabolism in Glioblastoma Multiforme
- Source :
- Anticancer research. 39(1)
- Publication Year :
- 2018
-
Abstract
- Background/aim Several epidemiological studies have reported the chemopreventive potential of biochanin A, in cancer development and progression. We investigated the anticancer potential of combination of biochanin A and temozolomide against U-87 MG and T98 G [glioblastoma multiforme (GBM)] cells. Materials and methods We evaluated the effect of biochanin A and temozolomide treatment on cell viability, expression of survival proteins, cell cycle, cell metabolism and mitochondrial function. Results Enhanced inhibitory effects of the combination treatment were observed on cell viability, expression of cell survival proteins EGFR, p-ERK, p-AKT, c-myc and MT-MMP1, and increased expression of the tumor suppressor, p-p53. Combination treatment also induced arrest in the G1 phase of the cell cycle. A shift in the metabolic phenotype of cells from glycolytic to oxidative phosphorylation was observed on combination treatment and the permeabilized cells showed a significant impairment in complex IV activity. Conclusion Biochanin A significantly enhanced the anticancer efficacy of temozolomide in GBM cells.
- Subjects :
- Cancer Research
Cell Survival
Apoptosis
Oxidative phosphorylation
law.invention
Biochanin A
03 medical and health sciences
chemistry.chemical_compound
Mice
0302 clinical medicine
law
Cell Line, Tumor
Antineoplastic Combined Chemotherapy Protocols
medicine
Temozolomide
Animals
Humans
Glycolysis
Viability assay
Cell Proliferation
Chemistry
General Medicine
Metabolism
Cell cycle
Genistein
Xenograft Model Antitumor Assays
Mitochondria
Gene Expression Regulation, Neoplastic
Oncology
030220 oncology & carcinogenesis
Cancer research
Suppressor
Glioblastoma
medicine.drug
Signal Transduction
Subjects
Details
- ISSN :
- 17917530
- Volume :
- 39
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Anticancer research
- Accession number :
- edsair.doi.dedup.....59a2b09afabc2726ef48df463f80804a