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We are analyzing https://link.springer.com/article/10.1186/1471-2407-7-55.

Title:
Novel markers for differentiation of lobular and ductal invasive breast carcinomas by laser microdissection and microarray analysis | BMC Cancer
Description:
Background Invasive ductal and lobular carcinomas (IDC and ILC) are the most common histological types of breast cancer. Clinical follow-up data and metastatic patterns suggest that the development and progression of these tumors are different. The aim of our study was to identify gene expression profiles of IDC and ILC in relation to normal breast epithelial cells. Methods We examined 30 samples (normal ductal and lobular cells from 10 patients, IDC cells from 5 patients, ILC cells from 5 patients) microdissected from cryosections of ten mastectomy specimens from postmenopausal patients. Fifty nanograms of total RNA were amplified and labeled by PCR and in vitro transcription. Samples were analysed upon Affymetrix U133 Plus 2.0 Arrays. The expression of seven differentially expressed genes (CDH1, EMP1, DDR1, DVL1, KRT5, KRT6, KRT17) was verified by immunohistochemistry on tissue microarrays. Expression of ASPN mRNA was validated by in situ hybridization on frozen sections, and CTHRC1, ASPN and COL3A1 were tested by PCR. Results Using GCOS pairwise comparison algorithm and rank products we have identified 84 named genes common to ILC versus normal cell types, 74 named genes common to IDC versus normal cell types, 78 named genes differentially expressed between normal ductal and lobular cells, and 28 named genes between IDC and ILC. Genes distinguishing between IDC and ILC are involved in epithelial-mesenchymal transition, TGF-beta and Wnt signaling. These changes were present in both tumor types but appeared to be more prominent in ILC. Immunohistochemistry for several novel markers (EMP1, DVL1, DDR1) distinguished large sets of IDC from ILC. Conclusion IDC and ILC can be differentiated both at the gene and protein levels. In this study we report two candidate genes, asporin (ASPN) and collagen triple helix repeat containing 1 (CTHRC1) which might be significant in breast carcinogenesis. Besides E-cadherin, the proteins validated on tissue microarrays (EMP1, DVL1, DDR1) may represent novel immunohistochemical markers helpful in distinguishing between IDC and ILC. Further studies with larger sets of patients are needed to verify the gene expression profiles of various histological types of breast cancer in order to determine molecular subclassifications, prognosis and the optimum treatment strategies.
Website Age:
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Custom-built

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🌠 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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Keywords {πŸ”}

cells, lobular, ductal, pubmed, expression, normal, tumor, article, google, scholar, cancer, gene, genes, breast, cas, analysis, carcinomas, carcinoma, cell, probe, sets, types, protein, microarray, expressed, wnt, pcr, differentially, pairwise, proteins, upregulated, involved, signaling, invasive, comparison, ecadherin, ilc, identified, profiles, patients, table, figure, central, tumors, idc, tissue, products, mammary, encoding, downregulated,

Topics {βœ’οΈ}

similar expression profile polyclonal rabbit anti-fitc/hrp c-erbb-b2/her2/neu genome-wide gene-expression profiles beta-catenin-independent wnt signaling open access article e-cadherin/catenin adhesion complex duct lobular unit mountain view author information authors diethyl pyrocarbonate-treated water article turashvili prkci encoding calcium-independent lef/tcr-binding sites stabilizes apc-catenin complexes high-throughput genetic analysis laser capture microdissection jan bouchal multi-omics analyses provide transforming growth factor-beta full size image leucine-rich repeat protein phospholipid-dependent protein kinase calcium-dependent serine endoprotease multi-analyst densitometric software article download pdf view src-family tyrosine kinases tgf-beta family members small leucine-rich proteoglycan lipid/fatty acid transport van de rijn breast-conservation therapy feasibility antibody-mediated signal amplification pre-publication history real-time quantitative pcr Ξ²-catenin-independent author correspondence functional wnt-frizzled complexes full genome analysis infiltrating duct carcinoma gene expression profiling leucine-rich repeat leucine rich repeat Ξ²-catenin-dependent akt/pkb pathway gene expression profiles gene-expression profiles hierarchical clustering based beta-catenin regulates

Questions {❓}

  • Is it different from infiltrating duct carcinoma?
  • Mersin H, Yildirim E, Gulben K, Berberoglu U: Is invasive lobular carcinoma different from invasive ductal carcinoma?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Novel markers for differentiation of lobular and ductal invasive breast carcinomas by laser microdissection and microarray analysis
         description:Invasive ductal and lobular carcinomas (IDC and ILC) are the most common histological types of breast cancer. Clinical follow-up data and metastatic patterns suggest that the development and progression of these tumors are different. The aim of our study was to identify gene expression profiles of IDC and ILC in relation to normal breast epithelial cells. We examined 30 samples (normal ductal and lobular cells from 10 patients, IDC cells from 5 patients, ILC cells from 5 patients) microdissected from cryosections of ten mastectomy specimens from postmenopausal patients. Fifty nanograms of total RNA were amplified and labeled by PCR and in vitro transcription. Samples were analysed upon Affymetrix U133 Plus 2.0 Arrays. The expression of seven differentially expressed genes (CDH1, EMP1, DDR1, DVL1, KRT5, KRT6, KRT17) was verified by immunohistochemistry on tissue microarrays. Expression of ASPN mRNA was validated by in situ hybridization on frozen sections, and CTHRC1, ASPN and COL3A1 were tested by PCR. Using GCOS pairwise comparison algorithm and rank products we have identified 84 named genes common to ILC versus normal cell types, 74 named genes common to IDC versus normal cell types, 78 named genes differentially expressed between normal ductal and lobular cells, and 28 named genes between IDC and ILC. Genes distinguishing between IDC and ILC are involved in epithelial-mesenchymal transition, TGF-beta and Wnt signaling. These changes were present in both tumor types but appeared to be more prominent in ILC. Immunohistochemistry for several novel markers (EMP1, DVL1, DDR1) distinguished large sets of IDC from ILC. IDC and ILC can be differentiated both at the gene and protein levels. In this study we report two candidate genes, asporin (ASPN) and collagen triple helix repeat containing 1 (CTHRC1) which might be significant in breast carcinogenesis. Besides E-cadherin, the proteins validated on tissue microarrays (EMP1, DVL1, DDR1) may represent novel immunohistochemical markers helpful in distinguishing between IDC and ILC. Further studies with larger sets of patients are needed to verify the gene expression profiles of various histological types of breast cancer in order to determine molecular subclassifications, prognosis and the optimum treatment strategies.
         datePublished:2007-03-27T00:00:00Z
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      headline:Novel markers for differentiation of lobular and ductal invasive breast carcinomas by laser microdissection and microarray analysis
      description:Invasive ductal and lobular carcinomas (IDC and ILC) are the most common histological types of breast cancer. Clinical follow-up data and metastatic patterns suggest that the development and progression of these tumors are different. The aim of our study was to identify gene expression profiles of IDC and ILC in relation to normal breast epithelial cells. We examined 30 samples (normal ductal and lobular cells from 10 patients, IDC cells from 5 patients, ILC cells from 5 patients) microdissected from cryosections of ten mastectomy specimens from postmenopausal patients. Fifty nanograms of total RNA were amplified and labeled by PCR and in vitro transcription. Samples were analysed upon Affymetrix U133 Plus 2.0 Arrays. The expression of seven differentially expressed genes (CDH1, EMP1, DDR1, DVL1, KRT5, KRT6, KRT17) was verified by immunohistochemistry on tissue microarrays. Expression of ASPN mRNA was validated by in situ hybridization on frozen sections, and CTHRC1, ASPN and COL3A1 were tested by PCR. Using GCOS pairwise comparison algorithm and rank products we have identified 84 named genes common to ILC versus normal cell types, 74 named genes common to IDC versus normal cell types, 78 named genes differentially expressed between normal ductal and lobular cells, and 28 named genes between IDC and ILC. Genes distinguishing between IDC and ILC are involved in epithelial-mesenchymal transition, TGF-beta and Wnt signaling. These changes were present in both tumor types but appeared to be more prominent in ILC. Immunohistochemistry for several novel markers (EMP1, DVL1, DDR1) distinguished large sets of IDC from ILC. IDC and ILC can be differentiated both at the gene and protein levels. In this study we report two candidate genes, asporin (ASPN) and collagen triple helix repeat containing 1 (CTHRC1) which might be significant in breast carcinogenesis. Besides E-cadherin, the proteins validated on tissue microarrays (EMP1, DVL1, DDR1) may represent novel immunohistochemical markers helpful in distinguishing between IDC and ILC. Further studies with larger sets of patients are needed to verify the gene expression profiles of various histological types of breast cancer in order to determine molecular subclassifications, prognosis and the optimum treatment strategies.
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      dateModified:2007-03-27T00:00:00Z
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      pageEnd:20
      license:https://creativecommons.org/licenses/by/2.0
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      keywords:
         Lobular Carcinoma
         Laser Capture Microdissection
         Rank Product
         Terminal Duct Lobular Unit
         Normal Cell Type
         Cancer Research
         Oncology
         Surgical Oncology
         Health Promotion and Disease Prevention
         Biomedicine
         general
         Medicine/Public Health
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            name:Eduard Fridman
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                     name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
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      name:Wenbin Wei
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               name:Cancer Research U.K. Institute of Cancer Studies, University of Birmingham, UK
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            address:
               name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Jiri Ehrmann
      affiliation:
            name:Institute of Pathology, Palacky University
            address:
               name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Jiri Klein
      affiliation:
            name:Palacky University
            address:
               name:Department of Surgery, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Eduard Fridman
      affiliation:
            name:Tel Aviv University, Chaim Sheba Medical Center and Sackler School of Medicine
            address:
               name:Department of Pathology, Tel Aviv University, Chaim Sheba Medical Center and Sackler School of Medicine, Tel Aviv, Israel
               type:PostalAddress
            type:Organization
      name:Jozef Skarda
      affiliation:
            name:Institute of Pathology, Palacky University
            address:
               name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Josef Srovnal
      affiliation:
            name:Palacky University
            address:
               name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Marian Hajduch
      affiliation:
            name:Palacky University
            address:
               name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
      name:Paul Murray
      affiliation:
            name:University of Birmingham
            address:
               name:Cancer Research U.K. Institute of Cancer Studies, University of Birmingham, UK
               type:PostalAddress
            type:Organization
      name:Zdenek Kolar
      affiliation:
            name:Institute of Pathology, Palacky University
            address:
               name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
      name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
      name:Cancer Research U.K. Institute of Cancer Studies, University of Birmingham, UK
      name:Cancer Research U.K. Institute of Cancer Studies, University of Birmingham, UK
      name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
      name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
      name:Department of Surgery, Palacky University, Olomouc, Czech Republic
      name:Department of Pathology, Tel Aviv University, Chaim Sheba Medical Center and Sackler School of Medicine, Tel Aviv, Israel
      name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic
      name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
      name:Laboratory of Experimental Medicine, Department of Pediatrics, Palacky University, Olomouc, Czech Republic
      name:Cancer Research U.K. Institute of Cancer Studies, University of Birmingham, UK
      name:Laboratory of Molecular Pathology, Institute of Pathology, Palacky University, Olomouc, Czech Republic

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