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Differential distributions of CSE1L/CAS and E-cadherin in the polarized and non-polarized epithelial glands of neoplastic colorectal epithelium
Colorectal glands are important functional organs in colorectal tissue and are also the origin of colorectal carcinomas. Epithelial cell polarization of colorectal glands is related to structural integrity and physiological functions of colorectal glands as well as colorectal carcinoma formation. Th...
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Published in: | Journal of molecular histology 2010-10, Vol.41 (4-5), p.259-266 |
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creator | Uen, Wu-Ching Tai, Cheng-Jeng Shen, Shing-Chuan Lee, Woan-Ruoh Tsao, Tang-Yi Deng, Win-Ping Chiou, Hung-Yi Hsu, Chung-Huei Hsieh, Cheng-I Liao, Ching-Fong Jiang, Ming-Chung |
description | Colorectal glands are important functional organs in colorectal tissue and are also the origin of colorectal carcinomas. Epithelial cell polarization of colorectal glands is related to structural integrity and physiological functions of colorectal glands as well as colorectal carcinoma formation. The cellular apoptosis susceptibility (CSE1L/CAS) protein has been shown to induce polarity formation of human colorectal cells in cell culture. E-cadherin expression in epithelial cells is crucial for the establishment and maintenance of epithelial cell polarity. In this study we examined the distributions of CSE1L and E-cadherin in the epithelial glands of normal and neoplastic colorectal epithelium and correlated these to polarity formation in the colorectal glands. Our results showed that CSE1L was differentially stained in the epithelial glands of neoplastic colorectal epithelium, and the staining was related to gland epithelial cell polarization and E-cadherin distribution. CSE1L was associated E-cadherin in GST pull-down experiments and immunoprecipitation assays. Basolateral staining of CSE1L and E-cadherin were seen in the polarized glands of normal and neoplastic colorectal epithelium. Absence of basolateral CSE1L staining in neoplastic epithelium glands was associated with loss of gland epithelial cell polarity, and this was parallel with E-cadherin staining. The non-polarized areas in epithelium glands showed a patchy staining for CSE1L and E-cadherin. These results indicate that examination of CSE1L and E-cadherin distribution in colorectal epithelium glands may be valuable for evaluating the malignance of colorectal disease. |
doi_str_mv | 10.1007/s10735-010-9286-2 |
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Epithelial cell polarization of colorectal glands is related to structural integrity and physiological functions of colorectal glands as well as colorectal carcinoma formation. The cellular apoptosis susceptibility (CSE1L/CAS) protein has been shown to induce polarity formation of human colorectal cells in cell culture. E-cadherin expression in epithelial cells is crucial for the establishment and maintenance of epithelial cell polarity. In this study we examined the distributions of CSE1L and E-cadherin in the epithelial glands of normal and neoplastic colorectal epithelium and correlated these to polarity formation in the colorectal glands. Our results showed that CSE1L was differentially stained in the epithelial glands of neoplastic colorectal epithelium, and the staining was related to gland epithelial cell polarization and E-cadherin distribution. CSE1L was associated E-cadherin in GST pull-down experiments and immunoprecipitation assays. Basolateral staining of CSE1L and E-cadherin were seen in the polarized glands of normal and neoplastic colorectal epithelium. Absence of basolateral CSE1L staining in neoplastic epithelium glands was associated with loss of gland epithelial cell polarity, and this was parallel with E-cadherin staining. The non-polarized areas in epithelium glands showed a patchy staining for CSE1L and E-cadherin. These results indicate that examination of CSE1L and E-cadherin distribution in colorectal epithelium glands may be valuable for evaluating the malignance of colorectal disease.</description><identifier>ISSN: 1567-2379</identifier><identifier>EISSN: 1567-2387</identifier><identifier>DOI: 10.1007/s10735-010-9286-2</identifier><identifier>PMID: 20734115</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : Springer Netherlands</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cadherins - metabolism ; Cell Biology ; Cell Line, Tumor ; Cell Polarity ; Cellular Apoptosis Susceptibility Protein - metabolism ; Colorectal epithelium ; colorectal neoplasms ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; CSE1L ; Developmental Biology ; E-cadherin ; Gland ; Humans ; Immunohistochemistry ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - pathology ; Life Sciences ; Original Paper ; Polarity ; Protein Binding</subject><ispartof>Journal of molecular histology, 2010-10, Vol.41 (4-5), p.259-266</ispartof><rights>Springer Science+Business Media B.V. 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-f1d1209a4b02fe5af13836d4b736f6939bfebab28b8640e0bf3fc0252d96ede03</citedby><cites>FETCH-LOGICAL-c394t-f1d1209a4b02fe5af13836d4b736f6939bfebab28b8640e0bf3fc0252d96ede03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20734115$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uen, Wu-Ching</creatorcontrib><creatorcontrib>Tai, Cheng-Jeng</creatorcontrib><creatorcontrib>Shen, Shing-Chuan</creatorcontrib><creatorcontrib>Lee, Woan-Ruoh</creatorcontrib><creatorcontrib>Tsao, Tang-Yi</creatorcontrib><creatorcontrib>Deng, Win-Ping</creatorcontrib><creatorcontrib>Chiou, Hung-Yi</creatorcontrib><creatorcontrib>Hsu, Chung-Huei</creatorcontrib><creatorcontrib>Hsieh, Cheng-I</creatorcontrib><creatorcontrib>Liao, Ching-Fong</creatorcontrib><creatorcontrib>Jiang, Ming-Chung</creatorcontrib><title>Differential distributions of CSE1L/CAS and E-cadherin in the polarized and non-polarized epithelial glands of neoplastic colorectal epithelium</title><title>Journal of molecular histology</title><addtitle>J Mol Hist</addtitle><addtitle>J Mol Histol</addtitle><description>Colorectal glands are important functional organs in colorectal tissue and are also the origin of colorectal carcinomas. Epithelial cell polarization of colorectal glands is related to structural integrity and physiological functions of colorectal glands as well as colorectal carcinoma formation. The cellular apoptosis susceptibility (CSE1L/CAS) protein has been shown to induce polarity formation of human colorectal cells in cell culture. E-cadherin expression in epithelial cells is crucial for the establishment and maintenance of epithelial cell polarity. In this study we examined the distributions of CSE1L and E-cadherin in the epithelial glands of normal and neoplastic colorectal epithelium and correlated these to polarity formation in the colorectal glands. Our results showed that CSE1L was differentially stained in the epithelial glands of neoplastic colorectal epithelium, and the staining was related to gland epithelial cell polarization and E-cadherin distribution. CSE1L was associated E-cadherin in GST pull-down experiments and immunoprecipitation assays. Basolateral staining of CSE1L and E-cadherin were seen in the polarized glands of normal and neoplastic colorectal epithelium. Absence of basolateral CSE1L staining in neoplastic epithelium glands was associated with loss of gland epithelial cell polarity, and this was parallel with E-cadherin staining. The non-polarized areas in epithelium glands showed a patchy staining for CSE1L and E-cadherin. These results indicate that examination of CSE1L and E-cadherin distribution in colorectal epithelium glands may be valuable for evaluating the malignance of colorectal disease.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cadherins - metabolism</subject><subject>Cell Biology</subject><subject>Cell Line, Tumor</subject><subject>Cell Polarity</subject><subject>Cellular Apoptosis Susceptibility Protein - metabolism</subject><subject>Colorectal epithelium</subject><subject>colorectal neoplasms</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>CSE1L</subject><subject>Developmental Biology</subject><subject>E-cadherin</subject><subject>Gland</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - pathology</subject><subject>Life Sciences</subject><subject>Original Paper</subject><subject>Polarity</subject><subject>Protein Binding</subject><issn>1567-2379</issn><issn>1567-2387</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EoqXwAGwgYsPK1D9JHC-rYQpII7EYurbs-HrqKmMHO1mUl-CV6zT9kVggWbLl853jax2E3lPyhRIizjMlgjeYUIIl61rMXqBT2rQCM96Jl09nIU_Qm5xvCClQLV-jE1Z8NaXNKfr71TsHCcLk9VBZn6fkzTz5GHIVXbXZb-nufHOxr3Sw1Rb32l5D8qEqa7qGaoyDTv4P2Hs9xICfb2D0BRmW3MNQ5PvAAHEcdJ58X_VxiAn6qeiP6Hx8i145PWR497CfoavL7a_Nd7z7-e3H5mKHey7rCTtqKSNS14YwB412lHe8tbURvHWt5NI4MNqwzpQfEyDGcdcT1jArW7BA-Bn6vOaOKf6eIU_q6HMPQxkU4pyVaBoqWNOyQn76h7yJcwpluALVtJZSLBBdoT7FnBM4NSZ_1OlWUaKWrtTalSpdqaUrtXg-PATP5gj2yfFYTgHYCuQihQOk55f_l_pxNTkdlT4kn9XVnhHKCe0kJ-VwB4L7qdU</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Uen, Wu-Ching</creator><creator>Tai, Cheng-Jeng</creator><creator>Shen, Shing-Chuan</creator><creator>Lee, Woan-Ruoh</creator><creator>Tsao, Tang-Yi</creator><creator>Deng, Win-Ping</creator><creator>Chiou, Hung-Yi</creator><creator>Hsu, Chung-Huei</creator><creator>Hsieh, Cheng-I</creator><creator>Liao, Ching-Fong</creator><creator>Jiang, Ming-Chung</creator><general>Dordrecht : Springer Netherlands</general><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20101001</creationdate><title>Differential distributions of CSE1L/CAS and E-cadherin in the polarized and non-polarized epithelial glands of neoplastic colorectal epithelium</title><author>Uen, Wu-Ching ; Tai, Cheng-Jeng ; Shen, Shing-Chuan ; Lee, Woan-Ruoh ; Tsao, Tang-Yi ; Deng, Win-Ping ; Chiou, Hung-Yi ; Hsu, Chung-Huei ; Hsieh, Cheng-I ; Liao, Ching-Fong ; Jiang, Ming-Chung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-f1d1209a4b02fe5af13836d4b736f6939bfebab28b8640e0bf3fc0252d96ede03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cadherins - metabolism</topic><topic>Cell Biology</topic><topic>Cell Line, Tumor</topic><topic>Cell Polarity</topic><topic>Cellular Apoptosis Susceptibility Protein - metabolism</topic><topic>Colorectal epithelium</topic><topic>colorectal neoplasms</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>CSE1L</topic><topic>Developmental Biology</topic><topic>E-cadherin</topic><topic>Gland</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - pathology</topic><topic>Life Sciences</topic><topic>Original Paper</topic><topic>Polarity</topic><topic>Protein Binding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uen, Wu-Ching</creatorcontrib><creatorcontrib>Tai, Cheng-Jeng</creatorcontrib><creatorcontrib>Shen, Shing-Chuan</creatorcontrib><creatorcontrib>Lee, Woan-Ruoh</creatorcontrib><creatorcontrib>Tsao, Tang-Yi</creatorcontrib><creatorcontrib>Deng, Win-Ping</creatorcontrib><creatorcontrib>Chiou, Hung-Yi</creatorcontrib><creatorcontrib>Hsu, Chung-Huei</creatorcontrib><creatorcontrib>Hsieh, Cheng-I</creatorcontrib><creatorcontrib>Liao, Ching-Fong</creatorcontrib><creatorcontrib>Jiang, Ming-Chung</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - 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Epithelial cell polarization of colorectal glands is related to structural integrity and physiological functions of colorectal glands as well as colorectal carcinoma formation. The cellular apoptosis susceptibility (CSE1L/CAS) protein has been shown to induce polarity formation of human colorectal cells in cell culture. E-cadherin expression in epithelial cells is crucial for the establishment and maintenance of epithelial cell polarity. In this study we examined the distributions of CSE1L and E-cadherin in the epithelial glands of normal and neoplastic colorectal epithelium and correlated these to polarity formation in the colorectal glands. Our results showed that CSE1L was differentially stained in the epithelial glands of neoplastic colorectal epithelium, and the staining was related to gland epithelial cell polarization and E-cadherin distribution. CSE1L was associated E-cadherin in GST pull-down experiments and immunoprecipitation assays. Basolateral staining of CSE1L and E-cadherin were seen in the polarized glands of normal and neoplastic colorectal epithelium. Absence of basolateral CSE1L staining in neoplastic epithelium glands was associated with loss of gland epithelial cell polarity, and this was parallel with E-cadherin staining. The non-polarized areas in epithelium glands showed a patchy staining for CSE1L and E-cadherin. These results indicate that examination of CSE1L and E-cadherin distribution in colorectal epithelium glands may be valuable for evaluating the malignance of colorectal disease.</abstract><cop>Dordrecht</cop><pub>Dordrecht : Springer Netherlands</pub><pmid>20734115</pmid><doi>10.1007/s10735-010-9286-2</doi><tpages>8</tpages></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Cadherins - metabolism Cell Biology Cell Line, Tumor Cell Polarity Cellular Apoptosis Susceptibility Protein - metabolism Colorectal epithelium colorectal neoplasms Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology CSE1L Developmental Biology E-cadherin Gland Humans Immunohistochemistry Intestinal Mucosa - metabolism Intestinal Mucosa - pathology Life Sciences Original Paper Polarity Protein Binding |
title | Differential distributions of CSE1L/CAS and E-cadherin in the polarized and non-polarized epithelial glands of neoplastic colorectal epithelium |
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