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We began analyzing https://www.nature.com/articles/1209254, but it redirected us to https://www.nature.com/articles/1209254. The analysis below is for the second page.

Title[redir]:
Gene expression profiling of breast cell lines identifies potential new basal markers | Oncogene
Description:
A better molecular characterization of breast cell lines (BCL) may help discover new markers to apply to tumour samples. We performed gene and protein expression profiling of 31 BCL using whole-genome DNA microarrays and immunohistochemistry (IHC) on ‘cell microarrays’ (CMA), respectively. Global hierarchical clustering discriminated two groups of BCL: group I corresponded to luminal cell lines, group II to basal and mesenchymal cell lines. Correlations with centroids calculated from a published ‘intrinsic 500-gene set’ assigned 15 cell lines as luminal, eight as basal and four as mesenchymal. A set of 1.233 genes was differentially expressed between basal and luminal samples. Mesenchymal and basal subtypes were rather similar and discriminated by only 227 genes. The expression of 10 proteins (CAV1, CD44, EGFR, MET, ETS1, GATA3, luminal cytokeratin CK19, basal cytokeratin CK5/6, CD10, and ERM protein moesin) encoded by luminal vs basal discriminator genes confirmed the subtype classification and the validity of the identified markers. Our BCL basal/luminal signature correctly re-classified the published series of tumour samples that originally served to identify the molecular subtypes, suggesting that the identified markers should be useful for tumour classification and might represent promising targets for disease management.

Matching Content Categories {📚}

  • Health & Fitness
  • Science
  • Telecommunications

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?

🏙️ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 80,479,999 visitors per month in the current month.

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While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Doi.org could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

cancer, breast, nature, cell, charafejauffret, access, article, bertucci, res, oncogene, basal, ginestier, supplementary, content, lines, genes, natl, research, cookies, information, expression, markers, jacquemier, luminal, int, sci, marseille, privacy, open, proc, acad, usa, data, published, gene, profiling, finetti, birnbaum, bcl, subtypes, cells, sorlie, tumor, paolicalmettes, author, france, table, xls, advertising, journal,

Topics {✒️}

nature portfolio permissions reprints privacy policy nature 406 nature advertising cancer research 65 luminal-type breast cancer umr599 inserm/institut paoli-calmettes social media triple-negative breast cancer research breast cell lines inserm/institut paoli-calmettes gene expression profiling luminal cell lines personal data protein expression profiling genome dna microarrays author correspondence springerlink instant access breast cancer subtypes data protection permissions differential chromatin accessibility mesenchymal cell lines institut paoli-calmettes springer el privacy published series luminal cytokeratin ck19 issue learn medical oncology breast cancer supplementary figure legend explore content subscription content basal cytokeratin ck5/6 article charafe-jauffret van de rm de koster cg ufr de médecine european economic area erm protein moesin represent promising targets institutional subscriptions read o'hare mj beazer-barclay yd marseille cancer institute accepting optional cookies

Schema {🗺️}

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         headline:Gene expression profiling of breast cell lines identifies potential new basal markers
         description:A better molecular characterization of breast cell lines (BCL) may help discover new markers to apply to tumour samples. We performed gene and protein expression profiling of 31 BCL using whole-genome DNA microarrays and immunohistochemistry (IHC) on ‘cell microarrays’ (CMA), respectively. Global hierarchical clustering discriminated two groups of BCL: group I corresponded to luminal cell lines, group II to basal and mesenchymal cell lines. Correlations with centroids calculated from a published ‘intrinsic 500-gene set’ assigned 15 cell lines as luminal, eight as basal and four as mesenchymal. A set of 1.233 genes was differentially expressed between basal and luminal samples. Mesenchymal and basal subtypes were rather similar and discriminated by only 227 genes. The expression of 10 proteins (CAV1, CD44, EGFR, MET, ETS1, GATA3, luminal cytokeratin CK19, basal cytokeratin CK5/6, CD10, and ERM protein moesin) encoded by luminal vs basal discriminator genes confirmed the subtype classification and the validity of the identified markers. Our BCL basal/luminal signature correctly re-classified the published series of tumour samples that originally served to identify the molecular subtypes, suggesting that the identified markers should be useful for tumour classification and might represent promising targets for disease management.
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      headline:Gene expression profiling of breast cell lines identifies potential new basal markers
      description:A better molecular characterization of breast cell lines (BCL) may help discover new markers to apply to tumour samples. We performed gene and protein expression profiling of 31 BCL using whole-genome DNA microarrays and immunohistochemistry (IHC) on ‘cell microarrays’ (CMA), respectively. Global hierarchical clustering discriminated two groups of BCL: group I corresponded to luminal cell lines, group II to basal and mesenchymal cell lines. Correlations with centroids calculated from a published ‘intrinsic 500-gene set’ assigned 15 cell lines as luminal, eight as basal and four as mesenchymal. A set of 1.233 genes was differentially expressed between basal and luminal samples. Mesenchymal and basal subtypes were rather similar and discriminated by only 227 genes. The expression of 10 proteins (CAV1, CD44, EGFR, MET, ETS1, GATA3, luminal cytokeratin CK19, basal cytokeratin CK5/6, CD10, and ERM protein moesin) encoded by luminal vs basal discriminator genes confirmed the subtype classification and the validity of the identified markers. Our BCL basal/luminal signature correctly re-classified the published series of tumour samples that originally served to identify the molecular subtypes, suggesting that the identified markers should be useful for tumour classification and might represent promising targets for disease management.
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         breast cancer
         DNA microarray
         epithelium
         expression profiling
         luminal
         breast cell lines
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         general
         Internal Medicine
         Cell Biology
         Human Genetics
         Oncology
         Apoptosis
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