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breast, google, scholar, article, pubmed, cancer, cas, expression, ctcf, lobular, carcinoma, gene, ecadherin, genes, situ, lcis, res, loss, invasive, cdh, analysis, green, ellis, normal, access, cell, pathol, privacy, cookies, content, research, chromosome, dpep, factor, ductal, biol, lobanenkov, data, publish, search, andrew, rakha, paish, powe, cases, cletonjansen, human, van, mutations, zinc,

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month download article/chapter mammalian c-myc oncogenes laser capture microdissection transcription factor ctcf real-time pcr analysis mccarty ks sr paraffin-embedded biopsies full article pdf walborg ef jr privacy choices/manage cookies zinc finger mutations real-time pcr methylation profiles cell growth inhibition thick tissue specimens normal breast tissue invasive breast cancer candidate gene located human e-cadherin lobular breast cancer e-cadherin alterations dpep1 gene expression paraffin processed lcis tumour suppressor genes atypical ductal hyperplasia european economic area columnar cell lesions amo-takyi bk comparative genomic hybridization de leeuw wj filippova gn morse hc 3rd glutathione-degrading enzymes blanchette-mackie ej monoclonal antireceptor antibodies formalin-fixed barcellos-hoff mh ortiz-de-solorzano ter haar nt e-cadherin inactivation kidney complementary dnas subtractive hybridization approach normal breast lobules molecular medical sciences invasive tubular carcinoma ctcf gene mutations conditions privacy policy atypical lobular hyperplasia scott-conner ce reis-filho js

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• Cleton-Jansen AM (2002) E-cadherin and loss of heterozygosity at chromosome 16 in breast carcinogenesis: different genetic pathways in ductal and lobular breast cancer?

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         headline:Loss of expression of chromosome 16q genes DPEP1 and CTCF in lobular carcinoma in situ of the breast
         description: Background Loss of the chromosomal material at 16q is the most frequent genetic event in invasive and in situ (LCIS) lobular carcinoma of the breast. However, the smallest region of overlap at 16q is not restricted to just the CDH1 locus harbouring E-cadherin, suggesting that neighbouring genes might be involved in the development and progression of these tumours. Potential novel tumour suppressor genes (TSG) at 16q include CCCTC-binding factor (CTCF), Decreased Expression in Renal and Prostate Cancer (DERPC) and Dipeptidase 1 (DPEP1). The aim of this study is to assess the expression of these genes in LCIS and compare them with normal breast, using CDH1 as a control, in order to evaluate their role as TSGs. Methods Cells from LCIS cases and normal breast lobules were microdissected and expression of target genes were quantified using real-time PCR. In addition, immunohistochemistry (IHC) for E-cadherin and CTCF was performed on paraffin processed LCIS (n = 49) and normal breast cases. Results All LCIS showed negative expression of E-cadherin. Similar to CDH1, CTCF and DPEP1 gene expression was significantly lower in LCIS cases compared with normal cases (P < 0.05). CTCF IHC expression showed significant reduction in LCIS compared to normal parenchymal cells. However, there was no difference in expression of DERPC between LCIS and normal breast tissue. Conclusions In addition to CDH1, loss of CTCF and DPEP1 gene expression suggest they are possible TSG in breast cancer and may, similar to CDH1, be potentially utilised as markers of predisposition of women diagnosed with LCIS.
         datePublished:2008-01-23T00:00:00Z
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         pageStart:59
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         sameAs:https://doi.org/10.1007/s10549-008-9905-8
         keywords:
            Lobular carcinoma in situ
            E-cadherin
            CCCTC-binding factor
            Dipeptidase 1
            Laser microdissection
            Oncology
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      headline:Loss of expression of chromosome 16q genes DPEP1 and CTCF in lobular carcinoma in situ of the breast
      description: Background Loss of the chromosomal material at 16q is the most frequent genetic event in invasive and in situ (LCIS) lobular carcinoma of the breast. However, the smallest region of overlap at 16q is not restricted to just the CDH1 locus harbouring E-cadherin, suggesting that neighbouring genes might be involved in the development and progression of these tumours. Potential novel tumour suppressor genes (TSG) at 16q include CCCTC-binding factor (CTCF), Decreased Expression in Renal and Prostate Cancer (DERPC) and Dipeptidase 1 (DPEP1). The aim of this study is to assess the expression of these genes in LCIS and compare them with normal breast, using CDH1 as a control, in order to evaluate their role as TSGs. Methods Cells from LCIS cases and normal breast lobules were microdissected and expression of target genes were quantified using real-time PCR. In addition, immunohistochemistry (IHC) for E-cadherin and CTCF was performed on paraffin processed LCIS (n = 49) and normal breast cases. Results All LCIS showed negative expression of E-cadherin. Similar to CDH1, CTCF and DPEP1 gene expression was significantly lower in LCIS cases compared with normal cases (P < 0.05). CTCF IHC expression showed significant reduction in LCIS compared to normal parenchymal cells. However, there was no difference in expression of DERPC between LCIS and normal breast tissue. Conclusions In addition to CDH1, loss of CTCF and DPEP1 gene expression suggest they are possible TSG in breast cancer and may, similar to CDH1, be potentially utilised as markers of predisposition of women diagnosed with LCIS.
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      pageEnd:66
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      keywords:
         Lobular carcinoma in situ
         E-cadherin
         CCCTC-binding factor
         Dipeptidase 1
         Laser microdissection
         Oncology
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