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  2. Matching Content Categories
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We are analyzing https://link.springer.com/article/10.1007/s10549-010-1280-6.

Title:
Different gene expressions are associated with the different molecular subtypes of inflammatory breast cancer | Breast Cancer Research and Treatment
Description:
The goal of this study was to determine whether gene expression differences exist between inflammatory breast cancers (IBC) and T stage-matched non-IBC patients stratified by hormone receptor and HER2 status. We used Affymetrix GeneChips to analyze 82 tumor samples (25 T4d patients, and 57 T4a-c patients) of newly diagnosed breast cancers. Genes that were differentially expressed between the IBC and non-IBC specimens were identified using the t test, and differential expression of gene sets was assessed using gene set analysis. Three distinct clinical subtypes of IBC and non-IBC were compared: ER-positive/HER2-normal, HER2-amplified, and ER-negative/HER2-normal. When we compared expression data from all IBC with all non-IBC, we found no significant differences after adjusting for multiple testing. When IBC and non-IBC tumors were compared by clinical subtype, however, significant differences emerged. Complement and immune system-related pathways were overexpressed in ER-positive/HER2-normal IBC. Protein translation and mTOR signaling were overexpressed in HER2-amplified IBC. Apoptosis-, neural-, and lipid metabolism-related pathways were overexpressed in ER-negative/HER2-normal IBC compared with non-IBC of the same receptor phenotype. In this T stage-matched case–control study, the survival curves of patients with IBC and non-IBC were similar for all three clinical subtypes. IBC tumors can be divided into molecular and clinical subtypes similar to those of non-IBC. Clinical subtypes of IBC show molecular differences compared with similar subtypes of non-IBC.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

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


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We're unsure if the website is profiting.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com has a revenue plan, but it's either invisible or we haven't found it.

Keywords {🔍}

cancer, breast, article, google, scholar, pubmed, cas, inflammatory, gene, molecular, ibc, anderson, analysis, expression, usa, clin, van, receptor, oncol, center, subtypes, nonibc, texas, university, res, houston, research, ueno, cell, department, supplementary, material, hortobagyi, pusztai, naoto, patients, access, clinical, study, compared, human, doijco, privacy, cookies, content, iwamoto, lajos, set, profiling, trastuzumab,

Topics {✒️}

er-negative/her2-normal ibc compared cdna microarray analysis er-positive/her2-normal ibc month download article/chapter stage-matched case–control study gene-expression profiling study er-positive/her2-normal er-negative/her2-normal her2-positive breast cancer mab-mediated cancer immunotherapy gene expression profiling gene set analysis cancer staging system lipid metabolism-related pathways gene expression analysis human breast cancer immune system-related pathways gene set enrichment dna-damaged induced apoptosis inflammatory breast cancers her2-overexpressing relapsed breast cancer based inflammatory breast cancer inflammatory breast cancer full article pdf commonwealth cancer foundation her2-targeted therapy oestrogen-receptor status privacy choices/manage cookies compared expression data breast medical oncology fredika robertson hormone receptor american joint committee van den eynden primary systemic therapy breast tumor heterogeneity distinct molecular signature molecular cytogenetic analysis rapamycin kinase inhibitor rapamycin inhibitor deforolimus knowledge-based approach van der auwera distinct clinical subtypes article iwamoto expanded her2+ cohort phase ii study lajos pusztai & naoto texas grant european economic area

Schema {🗺️}

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         headline:Different gene expressions are associated with the different molecular subtypes of inflammatory breast cancer
         description:The goal of this study was to determine whether gene expression differences exist between inflammatory breast cancers (IBC) and T stage-matched non-IBC patients stratified by hormone receptor and HER2 status. We used Affymetrix GeneChips to analyze 82 tumor samples (25 T4d patients, and 57 T4a-c patients) of newly diagnosed breast cancers. Genes that were differentially expressed between the IBC and non-IBC specimens were identified using the t test, and differential expression of gene sets was assessed using gene set analysis. Three distinct clinical subtypes of IBC and non-IBC were compared: ER-positive/HER2-normal, HER2-amplified, and ER-negative/HER2-normal. When we compared expression data from all IBC with all non-IBC, we found no significant differences after adjusting for multiple testing. When IBC and non-IBC tumors were compared by clinical subtype, however, significant differences emerged. Complement and immune system-related pathways were overexpressed in ER-positive/HER2-normal IBC. Protein translation and mTOR signaling were overexpressed in HER2-amplified IBC. Apoptosis-, neural-, and lipid metabolism-related pathways were overexpressed in ER-negative/HER2-normal IBC compared with non-IBC of the same receptor phenotype. In this T stage-matched case–control study, the survival curves of patients with IBC and non-IBC were similar for all three clinical subtypes. IBC tumors can be divided into molecular and clinical subtypes similar to those of non-IBC. Clinical subtypes of IBC show molecular differences compared with similar subtypes of non-IBC.
         datePublished:2010-12-09T00:00:00Z
         dateModified:2010-12-09T00:00:00Z
         pageStart:785
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            Inflammatory breast cancer
            Receptor subtypes
            cDNA microarray
            Gene set analysis
            Oncology
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      headline:Different gene expressions are associated with the different molecular subtypes of inflammatory breast cancer
      description:The goal of this study was to determine whether gene expression differences exist between inflammatory breast cancers (IBC) and T stage-matched non-IBC patients stratified by hormone receptor and HER2 status. We used Affymetrix GeneChips to analyze 82 tumor samples (25 T4d patients, and 57 T4a-c patients) of newly diagnosed breast cancers. Genes that were differentially expressed between the IBC and non-IBC specimens were identified using the t test, and differential expression of gene sets was assessed using gene set analysis. Three distinct clinical subtypes of IBC and non-IBC were compared: ER-positive/HER2-normal, HER2-amplified, and ER-negative/HER2-normal. When we compared expression data from all IBC with all non-IBC, we found no significant differences after adjusting for multiple testing. When IBC and non-IBC tumors were compared by clinical subtype, however, significant differences emerged. Complement and immune system-related pathways were overexpressed in ER-positive/HER2-normal IBC. Protein translation and mTOR signaling were overexpressed in HER2-amplified IBC. Apoptosis-, neural-, and lipid metabolism-related pathways were overexpressed in ER-negative/HER2-normal IBC compared with non-IBC of the same receptor phenotype. In this T stage-matched case–control study, the survival curves of patients with IBC and non-IBC were similar for all three clinical subtypes. IBC tumors can be divided into molecular and clinical subtypes similar to those of non-IBC. Clinical subtypes of IBC show molecular differences compared with similar subtypes of non-IBC.
      datePublished:2010-12-09T00:00:00Z
      dateModified:2010-12-09T00:00:00Z
      pageStart:785
      pageEnd:795
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         Inflammatory breast cancer
         Receptor subtypes
         cDNA microarray
         Gene set analysis
         Oncology
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      author:
            name:Takayuki Iwamoto
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                     type:PostalAddress
                  type:Organization
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:Okayama University
                  address:
                     name:Department of Gastroenterological Surgery and Surgical Oncology, Okayama University, Okayama, Japan
                     type:PostalAddress
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            name:Giampaolo Bianchini
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Breast Cancer Translational Research Laboratory, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yuan Qi
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Massimo Cristofanilli
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
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            name:Anthony Lucci
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
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            name:Wendy A. Woodward
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Radiation Oncology Treatment, The University of Texas MD Anderson Cancer Center, Houston, USA
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            name:James M. Reuben
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Junji Matsuoka
            affiliation:
                  name:Okayama University
                  address:
                     name:Department of Gastroenterological Surgery and Surgical Oncology, Okayama University, Okayama, Japan
                     type:PostalAddress
                  type:Organization
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            name:Yun Gong
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
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            name:Savitri Krishnamurthy
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
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            name:Vicente Valero
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
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            name:Gabriel N. Hortobagyi
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                  address:
                     name:Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, Houston, USA
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            name:Fredika Robertson
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:W. Fraser Symmans
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Lajos Pusztai
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Breast Cancer Translational Research Laboratory, The University of Texas MD Anderson Cancer Center, Houston, USA
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                  address:
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                     type:PostalAddress
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            email:[email protected]
            type:Person
            name:Naoto T. Ueno
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Breast Cancer Translational Research Laboratory, The University of Texas MD Anderson Cancer Center, Houston, USA
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