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  2. Matching Content Categories
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We began analyzing https://link.springer.com/article/10.1007/s11010-010-0473-y, but it redirected us to https://link.springer.com/article/10.1007/s11010-010-0473-y. The analysis below is for the second page.

Title[redir]:
Demethylating agent 5-aza-2-deoxycytidine enhances susceptibility of breast cancer cells to anticancer agents | Molecular and Cellular Biochemistry
Description:
DNA methylation plays an important role in regulation of gene expression and is increasingly being recognized as a determinant of chemosensitivity of human cancers. With the aim of improving the chemotherapeutic efficacy of breast carcinoma, the effect of DNA methyltransferase inhibitor, 5-Aza-2′-deoxycytidine (5-aza-CdR), on the chemosensitivity of anticancer drugs was investigated. The cytotoxicity of paclitaxel (PTX), adriamycin (ADR), and 5-fluorouracil (5-FU) was analyzed against human breast cancer cell lines, MDA MB 231 and MCF 7 cell lines using the MTT assay, and the synergy of 5-aza-CdR and these agents was determined by Drewinko’s fraction method. The effects of each single agent or the combined treatment on cell cycle arrest were analyzed by flow cytometric analysis. We also investigated the effect of each single agent or the combined treatment of anticancer drugs with 5-aza-CdR on the methylation status of the selected genes by methylation specific PCR. In MDA MB 231 cells, a synergistic antiproliferative effect was observed with a combination of 10 μM 5-aza-CdR and these three anticancer drugs, while in MCF 7 cells, a semiadditive effect was observed. Treatment with 5-aza-CdR and anticancer drug resulted in partial demethylation of a panel of genes including RARβ2, Slit2, GSTP1, and MGMT. Based on these findings, we propose that 5-aza-CdR enhances the chemosensitivity of anticancer drugs in breast cancer cells and may be a promising approach for increasing the chemotherapeutic potential of these anticancer agents for more effective management of breast carcinomas.

Matching Content Categories {📚}

  • Science
  • Health & Fitness
  • Education

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 8,426,036 visitors per month in the current month.

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How Does Doi.org Make Money? {💸}

We're unsure if the website is profiting.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Doi.org could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

article, cancer, google, scholar, pubmed, cas, breast, anticancer, azadeoxycytidine, cell, methylation, human, agent, cells, drugs, treatment, dna, expression, azacdr, lines, privacy, cookies, content, agents, sharma, ranju, ralhan, gene, carcinoma, effect, access, res, lung, information, publish, search, demethylating, enhances, mirza, gayatri, chemosensitivity, drug, lee, analysis, data, log, journal, research, biochemistry, sameer,

Topics {✒️}

o6-methylguanine-dna methyltransferase gene month download article/chapter low-dose 5-aza-2′-deoxycytidine 5-aza-2′-deoxycytidine sensitizes hepatoma depressing p-glycoprotein activity promotes tnf-mediated apoptosis cellular biochemistry aims anticancer drug resulted 5-aza-cdr enhances full article pdf privacy choices/manage cookies dna methyltransferase inhibitor cell cycle arrest methylation specific pcr breast cancer cells prostate cancer detection ranju ralhan anti-cancer strategies anticancer agents published 10 μm 5-aza-cdr cyclin d2 expression gstp1 methylation analysis european economic area carbon metabolism pathways nonclonal neutrophil responses da silva nf tumor suppressor activity p53-induced apoptosis histone deacetylase inhibitor mount sinai hospital dna methylation article molecular article mirza 5-aza-2′-deoxycytidine genes including rarβ2 conditions privacy policy flow cytometric analysis check access drug combinations instant access gayatri sharma author information authors breast carcinoma accepting optional cookies drosophila slit2 gene single agent synergic antiproliferative effect combination chemotherapy article log synergistic antiproliferative effect

Schema {🗺️}

WebPage:
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         headline:Demethylating agent 5-aza-2-deoxycytidine enhances susceptibility of breast cancer cells to anticancer agents
         description:DNA methylation plays an important role in regulation of gene expression and is increasingly being recognized as a determinant of chemosensitivity of human cancers. With the aim of improving the chemotherapeutic efficacy of breast carcinoma, the effect of DNA methyltransferase inhibitor, 5-Aza-2′-deoxycytidine (5-aza-CdR), on the chemosensitivity of anticancer drugs was investigated. The cytotoxicity of paclitaxel (PTX), adriamycin (ADR), and 5-fluorouracil (5-FU) was analyzed against human breast cancer cell lines, MDA MB 231 and MCF 7 cell lines using the MTT assay, and the synergy of 5-aza-CdR and these agents was determined by Drewinko’s fraction method. The effects of each single agent or the combined treatment on cell cycle arrest were analyzed by flow cytometric analysis. We also investigated the effect of each single agent or the combined treatment of anticancer drugs with 5-aza-CdR on the methylation status of the selected genes by methylation specific PCR. In MDA MB 231 cells, a synergistic antiproliferative effect was observed with a combination of 10 μM 5-aza-CdR and these three anticancer drugs, while in MCF 7 cells, a semiadditive effect was observed. Treatment with 5-aza-CdR and anticancer drug resulted in partial demethylation of a panel of genes including RARβ2, Slit2, GSTP1, and MGMT. Based on these findings, we propose that 5-aza-CdR enhances the chemosensitivity of anticancer drugs in breast cancer cells and may be a promising approach for increasing the chemotherapeutic potential of these anticancer agents for more effective management of breast carcinomas.
         datePublished:2010-05-09T00:00:00Z
         dateModified:2010-05-09T00:00:00Z
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            Breast carcinoma
            Anticancer agents
            Chemosensitivity
            Biochemistry
            general
            Cardiology
            Cancer Research
            Medical Biochemistry
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      headline:Demethylating agent 5-aza-2-deoxycytidine enhances susceptibility of breast cancer cells to anticancer agents
      description:DNA methylation plays an important role in regulation of gene expression and is increasingly being recognized as a determinant of chemosensitivity of human cancers. With the aim of improving the chemotherapeutic efficacy of breast carcinoma, the effect of DNA methyltransferase inhibitor, 5-Aza-2′-deoxycytidine (5-aza-CdR), on the chemosensitivity of anticancer drugs was investigated. The cytotoxicity of paclitaxel (PTX), adriamycin (ADR), and 5-fluorouracil (5-FU) was analyzed against human breast cancer cell lines, MDA MB 231 and MCF 7 cell lines using the MTT assay, and the synergy of 5-aza-CdR and these agents was determined by Drewinko’s fraction method. The effects of each single agent or the combined treatment on cell cycle arrest were analyzed by flow cytometric analysis. We also investigated the effect of each single agent or the combined treatment of anticancer drugs with 5-aza-CdR on the methylation status of the selected genes by methylation specific PCR. In MDA MB 231 cells, a synergistic antiproliferative effect was observed with a combination of 10 μM 5-aza-CdR and these three anticancer drugs, while in MCF 7 cells, a semiadditive effect was observed. Treatment with 5-aza-CdR and anticancer drug resulted in partial demethylation of a panel of genes including RARβ2, Slit2, GSTP1, and MGMT. Based on these findings, we propose that 5-aza-CdR enhances the chemosensitivity of anticancer drugs in breast cancer cells and may be a promising approach for increasing the chemotherapeutic potential of these anticancer agents for more effective management of breast carcinomas.
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         Anticancer agents
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         Cancer Research
         Medical Biochemistry
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      name:Department of Otolaryngology-Head and Neck Surgery, Mount Sinai Hospital, University of Toronto, Toronto, Canada
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External Links {🔗}(137)

Analytics and Tracking {📊}

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Libraries {📚}

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Mail Servers:

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CDN Services {📦}

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