2012
DOI: 10.7314/apjcp.2012.13.12.6511
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Iris Nertschinskia Ethanol Extract Differentially Induces Cytotoxicity in Human Breast Cancer Cells Depending on AKT1/2 Activity

Abstract: Recently, we reported that an ethanol extract of Iris nertschinskia induces p53-dependent apoptosis in the MCF7 human breast cancer cell line. However, the detailed mechanisms were not fully explored. Here, we demonstrate another aspect of the activity of I. nertschinskia in breast cancer cells. We compared the response to an ethanol extract of I. nertschinskia in two different human breast cancer cell lines, Hs578Tand MDA-MB231, respectively with relatively low and high AKT1/2 activity by trypan blue exclusio… Show more

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Cited by 4 publications
(6 citation statements)
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References 26 publications
(22 reference statements)
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“…A lot of antitumor drugs were derived from plants or traditional medicine, which were used to treat the disease as different folk medicine for a long time, so new drug discovery from herbs is more likely to succeed (Shin et al, 2012;Huang et al, 2013). Rabdosia rubescens has been used as an herbal remedy for various ailments including cancer in China, and oridonin is one of the anticancer components of Rabdosia rubescens.…”
Section: Discussionmentioning
confidence: 99%
“…A lot of antitumor drugs were derived from plants or traditional medicine, which were used to treat the disease as different folk medicine for a long time, so new drug discovery from herbs is more likely to succeed (Shin et al, 2012;Huang et al, 2013). Rabdosia rubescens has been used as an herbal remedy for various ailments including cancer in China, and oridonin is one of the anticancer components of Rabdosia rubescens.…”
Section: Discussionmentioning
confidence: 99%
“…However, this effect may depend on the degree of malignancy of the cancer cell line. Shin et al [ 36 ] observed that an ethanol extract of Xiphion orientale Schrank (syn. Iris nertschinskia G.…”
Section: Resultsmentioning
confidence: 99%
“…The accumulation of cells in the sub-G 1 phase is an apoptotic characteristic and may be determined using a fluorescence-activated cell sorting (FACS) method, as previously described (28)(29)(30). Briefly, control (DBTRG cells without RC-RNase treatment) and experimental cells (DBTRG cells with 20 ug/ml RC-RNase treatment) were fixed with 70% alcohol at 4˚C for 1 h. The fixed cells were washed with phosphate-buffered saline (PBS) and treated with 1 ml propidium iodide (PI) solution, containing 50 µg/ml PI, 100 µg/ml RNase A and 0.1% Triton X-100, at 37˚C for 1 h. Following the PBS wash, these cells were analyzed by flow cytometry, which was performed using the CyFlow SL flow cytometer and Flomax software from Sysmex Partec GmbH (Görlitz, Görlitz, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…Therefore, RC-RNase may induce apoptotic cell death in DBTRG cells. Additionally, the apoptotic characteristic of cells accumulating in the sub-G 1 phase was identified following 72 h of treatment in the RC-RNase-treated DBTRG cells, which was determined using a FACS analysis method as previously described (28)(29)(30). As Fig.…”
Section: Rc-r Nase Induces Apoptosis a Nd Activation Of Caspases-9 Anmentioning
confidence: 99%