DOI . ORG {
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We began analyzing https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0028068, but it redirected us to https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0028068. The analysis below is for the second page.
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Description:
Metformin, a Type II diabetic treatment drug, which inhibits transcription of gluconeogenesis genes, has recently been shown to lower the risk of some diabetes-related tumors, including breast cancer. Recently, “cancer stem cells” have been demonstrated to sustain the growth of tumors and are resistant to therapy. To test the hypothesis that metformin might be reducing the risk to breast cancers, the human breast carcinoma cell line, MCF-7, grown in 3-dimensional mammospheres which represent human breast cancer stem cell population, were treated with various known and suspected breast cancer chemicals with and without non-cytotoxic concentrations of metformin. Using OCT4 expression as a marker for the cancer stem cells, the number and size were measured in these cells. Results demonstrated that TCDD (100 nM) and bisphenol A (10 µM) increased the number and size of the mammospheres, as did estrogen (10 nM E2). By monitoring a cancer stem cell marker, OCT4, the stimulation by these chemicals was correlated with the increased expression of OCT4. On the other hand, metformin at 1 and 10 mM concentration dramatically reduced the size and number of mammospheres. Results also demonstrated the metformin reduced the expression of OCT4 in E2 & TCDD mammospheres but not in the bisphenol A mammospheres, suggesting different mechanisms of action of the bisphenol A on human breast carcinoma cells. In addition, these results support the use of 3-dimensional human breast cancer stem cells as a means to screen for potential human breast tumor promoters and breast chemopreventive and chemotherapeutic agents.
Title[redir]:
No title found...
Description:
Metformin, a Type II diabetic treatment drug, which inhibits transcription of gluconeogenesis genes, has recently been shown to lower the risk of some diabetes-related tumors, including breast cancer. Recently, “cancer stem cells” have been demonstrated to sustain the growth of tumors and are resistant to therapy. To test the hypothesis that metformin might be reducing the risk to breast cancers, the human breast carcinoma cell line, MCF-7, grown in 3-dimensional mammospheres which represent human breast cancer stem cell population, were treated with various known and suspected breast cancer chemicals with and without non-cytotoxic concentrations of metformin. Using OCT4 expression as a marker for the cancer stem cells, the number and size were measured in these cells. Results demonstrated that TCDD (100 nM) and bisphenol A (10 µM) increased the number and size of the mammospheres, as did estrogen (10 nM E2). By monitoring a cancer stem cell marker, OCT4, the stimulation by these chemicals was correlated with the increased expression of OCT4. On the other hand, metformin at 1 and 10 mM concentration dramatically reduced the size and number of mammospheres. Results also demonstrated the metformin reduced the expression of OCT4 in E2 & TCDD mammospheres but not in the bisphenol A mammospheres, suggesting different mechanisms of action of the bisphenol A on human breast carcinoma cells. In addition, these results support the use of 3-dimensional human breast cancer stem cells as a means to screen for potential human breast tumor promoters and breast chemopreventive and chemotherapeutic agents.
Matching Content Categories {📚}
- Education
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Doi.org is powered by WORDPRESS.
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Keywords {🔍}
cancer, cells, oct, mammospheres, metformin, breast, mcf, cell, stem, article, view, expression, google, scholar, estrogen, human, tcdd, mammosphere, figure, treatment, phenol, gene, bpa, promoter, growth, increased, plos, number, formation, res, results, msv, transcription, proliferation, ere, binding, tumor, study, effect, image, line, treated, concentrations, bisphenol, concentration, receptor, sequences, type, size, showed,
Topics {✒️}
health canada oct4 promoter regions cookies plos er-estrogen complex plos pbp/trap220/drip205 subunit interacts open-access article distributed contributed reagents/materials/analysis tools fundamental biology molecular biology antioxidant n-acetyl-l-cysteine stem/progenitor cell properties biology n-acetyl-l-cysteine oxidative stress-induced signaling il-1α promoter region population-based case-control study therapy steroid receptor-positive cells �cancer stem cells” cancer stem cells intra-cellular signal transductors short-term clinical trial putative cis-regulatory elements breast tumor promoters stem cell theory stem cell characteristics human breast cancer adult stem cells epithelial cell line breast cancer cells estrogen receptor-independent pathway er-positive human mammospheres breast cancer promoting breast carcinoma cells early stem cells human breast cells breast cancer promoters �tumor-sustaining” cells �kill” tumor cells original author estrogen receptor-dependent pathway sv40-transformed immortal type cd44+cd24- cells including breast cancer estrogen receptor-regulated transcription el800 microplate reader human oct4 promoter tumor promoting chemicals endogenous tumor initiators
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