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Silencing of the CD44 Gene by CpG Methylation in a Human Gastric Carcinoma Cell Line
We analyzed 8 human gastric carcinoma cell lines for the expression of CD44 by northern blot analysis and reverse transcription‐polymerase chain reaction (RT‐PCR), and identified 1 cell line MKN‐28 that did not express CD44. In an attempt to clarify the mechanism responsible for the inactivation of...
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Published in: | Cancer science 1999-05, Vol.90 (5), p.485-489 |
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creator | Sato, Sunao Yokozaki, Hiroshi Yasui, Wataru Nikai, Hiromasa Tahara, Eiichi |
description | We analyzed 8 human gastric carcinoma cell lines for the expression of CD44 by northern blot analysis and reverse transcription‐polymerase chain reaction (RT‐PCR), and identified 1 cell line MKN‐28 that did not express CD44. In an attempt to clarify the mechanism responsible for the inactivation of CD44 gene expression in this cell line, we investigated the methylation status around the promoter region of CD44 gene by digestion of the DNA with the methylation‐sensitive restriction enzyme Hpa II. The promoter region of CD44 in MKN‐28 revealed hypermethylation, whereas other CD44‐positive cell lines did not. Furthermore, treatment of MKN‐28 with the demethylating agent 5‐azacytidine restored the expression of the gene. These results suggest that CD44 expression is controlled by a DNA hypermethylation mechanism in MKN‐28. |
doi_str_mv | 10.1111/j.1349-7006.1999.tb00773.x |
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In an attempt to clarify the mechanism responsible for the inactivation of CD44 gene expression in this cell line, we investigated the methylation status around the promoter region of CD44 gene by digestion of the DNA with the methylation‐sensitive restriction enzyme Hpa II. The promoter region of CD44 in MKN‐28 revealed hypermethylation, whereas other CD44‐positive cell lines did not. Furthermore, treatment of MKN‐28 with the demethylating agent 5‐azacytidine restored the expression of the gene. 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In an attempt to clarify the mechanism responsible for the inactivation of CD44 gene expression in this cell line, we investigated the methylation status around the promoter region of CD44 gene by digestion of the DNA with the methylation‐sensitive restriction enzyme Hpa II. The promoter region of CD44 in MKN‐28 revealed hypermethylation, whereas other CD44‐positive cell lines did not. Furthermore, treatment of MKN‐28 with the demethylating agent 5‐azacytidine restored the expression of the gene. These results suggest that CD44 expression is controlled by a DNA hypermethylation mechanism in MKN‐28.</description><subject>Azacytidine</subject><subject>Biological and medical sciences</subject><subject>CD44</subject><subject>CD44 antigen</subject><subject>CpG islands</subject><subject>Deoxyribonucleic acid</subject><subject>Dinucleoside Phosphates</subject><subject>Dissemination</subject><subject>DNA</subject><subject>DNA Methylation</subject><subject>Gastric cancer</subject><subject>Gastric carcinoma</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic - physiology</subject><subject>Humans</subject><subject>Hyaluronan Receptors - genetics</subject><subject>Medical sciences</subject><subject>Methylation</subject><subject>Polymerase chain reaction</subject><subject>Promoter Regions, Genetic</subject><subject>Rapid Communication</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Reverse transcription</subject><subject>Stomach Neoplasms - genetics</subject><subject>Tumor cell</subject><subject>Tumor cell lines</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0910-5050</issn><issn>1347-9032</issn><issn>1349-7006</issn><issn>1876-4673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqVkcFu1DAQQCMEokvhF5AFiFvCOE7smEOlKpQt0iIOlLPlOJOuV4mz2Al0_x5Hu2oLN3wZyfNmNDMvSd5QyGh8H3YZZYVMBQDPqJQymxoAIVh29yRZ3aeeJiuQFNISSjhLXoSwA6ACeP48OaPAYqriq-Tmu-3RGetuydiRaYuk_lQUZI0OSXMg9X5NvuK0PfR6sqMj1hFNrudBO7LWYfLWkFr7WD4OmtTY92RjHb5MnnW6D_jqFM-TH5-vburrdPNt_aW-3KSG57JMG65BaN5KJhgtmZamg8qg4FTqjrEWiwY1Z0g7ni__eatbydEYg5VhEtl5cnHsu5-bAVuDbvK6V3tvB-0PatRW_Z1xdqtux1-qlDmnALHB-1MDP_6cMUxqsMHENbTDcQ6Ky4pTIYoIvv0H3I2zd3E5lRfxrkBztlAfj5TxYwgeu_tRKKhFndqpxY9a_KhFnTqpU3ex-PXjZR6VHl1F4N0J0MHovvM6egsPXAWC5fzhKL-j2cN_TKDqy6uiKtkf48C1FQ</recordid><startdate>199905</startdate><enddate>199905</enddate><creator>Sato, Sunao</creator><creator>Yokozaki, Hiroshi</creator><creator>Yasui, Wataru</creator><creator>Nikai, Hiromasa</creator><creator>Tahara, Eiichi</creator><general>Blackwell Publishing Ltd</general><general>Japanese Cancer Association</general><general>John Wiley & Sons, Inc</general><scope>IQODW</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>8FE</scope><scope>8FH</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199905</creationdate><title>Silencing of the CD44 Gene by CpG Methylation in a Human Gastric Carcinoma Cell Line</title><author>Sato, Sunao ; Yokozaki, Hiroshi ; Yasui, Wataru ; Nikai, Hiromasa ; Tahara, Eiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6295-b6a07a6d9373153a9cf08ce7619af33de4bea63e1f628ce72dad96eccce8c39e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Azacytidine</topic><topic>Biological and medical sciences</topic><topic>CD44</topic><topic>CD44 antigen</topic><topic>CpG islands</topic><topic>Deoxyribonucleic acid</topic><topic>Dinucleoside Phosphates</topic><topic>Dissemination</topic><topic>DNA</topic><topic>DNA Methylation</topic><topic>Gastric cancer</topic><topic>Gastric carcinoma</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic - physiology</topic><topic>Humans</topic><topic>Hyaluronan Receptors - genetics</topic><topic>Medical sciences</topic><topic>Methylation</topic><topic>Polymerase chain reaction</topic><topic>Promoter Regions, Genetic</topic><topic>Rapid Communication</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Reverse transcription</topic><topic>Stomach Neoplasms - genetics</topic><topic>Tumor cell</topic><topic>Tumor cell lines</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Sunao</creatorcontrib><creatorcontrib>Yokozaki, Hiroshi</creatorcontrib><creatorcontrib>Yasui, Wataru</creatorcontrib><creatorcontrib>Nikai, Hiromasa</creatorcontrib><creatorcontrib>Tahara, Eiichi</creatorcontrib><collection>Pascal-Francis</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 SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Sunao</au><au>Yokozaki, Hiroshi</au><au>Yasui, Wataru</au><au>Nikai, Hiromasa</au><au>Tahara, Eiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silencing of the CD44 Gene by CpG Methylation in a Human Gastric Carcinoma Cell Line</atitle><jtitle>Cancer science</jtitle><addtitle>Jpn J Cancer Res</addtitle><date>1999-05</date><risdate>1999</risdate><volume>90</volume><issue>5</issue><spage>485</spage><epage>489</epage><pages>485-489</pages><issn>0910-5050</issn><issn>1347-9032</issn><eissn>1349-7006</eissn><eissn>1876-4673</eissn><coden>GANNA2</coden><abstract>We analyzed 8 human gastric carcinoma cell lines for the expression of CD44 by northern blot analysis and reverse transcription‐polymerase chain reaction (RT‐PCR), and identified 1 cell line MKN‐28 that did not express CD44. In an attempt to clarify the mechanism responsible for the inactivation of CD44 gene expression in this cell line, we investigated the methylation status around the promoter region of CD44 gene by digestion of the DNA with the methylation‐sensitive restriction enzyme Hpa II. The promoter region of CD44 in MKN‐28 revealed hypermethylation, whereas other CD44‐positive cell lines did not. Furthermore, treatment of MKN‐28 with the demethylating agent 5‐azacytidine restored the expression of the gene. These results suggest that CD44 expression is controlled by a DNA hypermethylation mechanism in MKN‐28.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10391086</pmid><doi>10.1111/j.1349-7006.1999.tb00773.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Azacytidine Biological and medical sciences CD44 CD44 antigen CpG islands Deoxyribonucleic acid Dinucleoside Phosphates Dissemination DNA DNA Methylation Gastric cancer Gastric carcinoma Gene expression Gene Expression Regulation, Neoplastic - physiology Humans Hyaluronan Receptors - genetics Medical sciences Methylation Polymerase chain reaction Promoter Regions, Genetic Rapid Communication Reverse Transcriptase Polymerase Chain Reaction Reverse transcription Stomach Neoplasms - genetics Tumor cell Tumor cell lines Tumor Cells, Cultured Tumors |
title | Silencing of the CD44 Gene by CpG Methylation in a Human Gastric Carcinoma Cell Line |
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