2018
DOI: 10.1007/s10863-018-9750-3
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Ocimum basilicum but not Ocimum gratissimum present cytotoxic effects on human breast cancer cell line MCF-7, inducing apoptosis and triggering mTOR/Akt/p70S6K pathway

Abstract: Breast cancer is the major cause of death by cancer in women worldwide and in spite of the many drugs for its treatment, there is still the need for novel therapies for its control. Ocimum species have been used by traditional medicine to control several diseases, including cancer. We have previously characterized the antidiabetic properties of the unfractionated aqueous leaf extracts of Ocimum basilicum (OB) and Ocimum gratissimum (OG), modulating glucose metabolism in diabetic mice. Since glucose metabolism … Show more

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Cited by 34 publications
(16 citation statements)
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“…The five potent extracts activated apoptosis in MCF7 cells in a dose dependent manner (Figures 5 and 6). The apoptosis results are similar to other reports of the apoptotic effect of herbal products [28, 31, 32]. The plant extracts also induced cell cycle arrest at the S phase in MCF7 cells, which indicated that they caused DNA damage and irregularity in genome replication of the cells.…”
Section: Discussionsupporting
confidence: 89%
“…The five potent extracts activated apoptosis in MCF7 cells in a dose dependent manner (Figures 5 and 6). The apoptosis results are similar to other reports of the apoptotic effect of herbal products [28, 31, 32]. The plant extracts also induced cell cycle arrest at the S phase in MCF7 cells, which indicated that they caused DNA damage and irregularity in genome replication of the cells.…”
Section: Discussionsupporting
confidence: 89%
“…Apoptosis is another important process in the progression of tumors. Anticancer drugs and genes serve important roles in promoting the process of cancer apoptosis ( 38 - 40 ). Therefore, the effect of siASF1B on the apoptosis of PCa was analyzed.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, it is demonstrated that Rictor activation, and thus mTORC2 activation, facilitates the phosphorylation of Akt at T308 by PDK1, explaining our results 41 . Recently, we have shown that simultaneous activation of AMPK, mTORC1, mTORC2 and Akt pathways in cancer cells activate cell apoptosis, leading to cancer cell death 42 . In our current study, we found that the treatment of the animals with SA and ASA promoted the cleavage of Caspase 3 ( Fig.…”
Section: Resultsmentioning
confidence: 99%