Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma
AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors. METHODS: Specimens were collected surgically from seven patients with gastric adenocarcino...
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Veröffentlicht in: | World journal of gastroenterology : WJG 2006-10, Vol.12 (38), p.6207-6211 |
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creator | Calcagno, Danielle-Queiroz Leal, Mariana-Ferreira Seabra, Aline-Damaceno Khayat, Andre-Salim Chen, Elizabeth Suchi Demachki, Samia Assumpção, Paulo Pimentel Faria, Mario Henrique Girão Rabenhorst, Silvia Helena Barem Ferreira, Márcia Valéria Pitombeira de Arruda Cardoso Smith, Marília Burbano, Rommel-Rodríguez |
description | AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.
METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.
RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P 〈 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P 〈 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinaltype the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.
CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways. |
doi_str_mv | 10.3748/wjg.v12.i38.6207 |
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METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.
RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P 〈 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P 〈 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinaltype the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.
CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v12.i38.6207</identifier><identifier>PMID: 17036397</identifier><language>eng</language><publisher>United States: Genetics Division, Department of Morphology, Federal University of S(a)o Paulo, S(a)o Paulo, SP, Brazil</publisher><subject>Adenocarcinoma - genetics ; Adult ; Aged ; Aneuploidy ; Brazil ; Chromosomes, Human, Pair 8 ; Gene Amplification ; Gene Expression Regulation, Neoplastic ; Genes, myc ; Humans ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Middle Aged ; Rapid Communication ; Stomach Neoplasms - genetics ; 基因表达 ; 染色体 ; 病理机制</subject><ispartof>World journal of gastroenterology : WJG, 2006-10, Vol.12 (38), p.6207-6211</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>2006 Baishideng Publishing Group Co., Limited. All rights reserved. 2006</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-8e972240cf42b48ecb831b8d8c94fb6180a7094671ce42aad48c06d39d5188e33</citedby><cites>FETCH-LOGICAL-c408t-8e972240cf42b48ecb831b8d8c94fb6180a7094671ce42aad48c06d39d5188e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4088119/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4088119/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17036397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calcagno, Danielle-Queiroz</creatorcontrib><creatorcontrib>Leal, Mariana-Ferreira</creatorcontrib><creatorcontrib>Seabra, Aline-Damaceno</creatorcontrib><creatorcontrib>Khayat, Andre-Salim</creatorcontrib><creatorcontrib>Chen, Elizabeth Suchi</creatorcontrib><creatorcontrib>Demachki, Samia</creatorcontrib><creatorcontrib>Assumpção, Paulo Pimentel</creatorcontrib><creatorcontrib>Faria, Mario Henrique Girão</creatorcontrib><creatorcontrib>Rabenhorst, Silvia Helena Barem</creatorcontrib><creatorcontrib>Ferreira, Márcia Valéria Pitombeira</creatorcontrib><creatorcontrib>de Arruda Cardoso Smith, Marília</creatorcontrib><creatorcontrib>Burbano, Rommel-Rodríguez</creatorcontrib><title>Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.
METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.
RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P 〈 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P 〈 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinaltype the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.
CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways.</description><subject>Adenocarcinoma - genetics</subject><subject>Adult</subject><subject>Aged</subject><subject>Aneuploidy</subject><subject>Brazil</subject><subject>Chromosomes, Human, Pair 8</subject><subject>Gene Amplification</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes, myc</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Middle Aged</subject><subject>Rapid Communication</subject><subject>Stomach Neoplasms - genetics</subject><subject>基因表达</subject><subject>染色体</subject><subject>病理机制</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUcuO0zAUtRCIKQN7VshCiBUpfjVxNkhQ8RhpEBtYsLIc-6ZxSeyMnbQMP8Ov4tCKh2TJi_O4596D0GNK1rwS8uVxv1sfKFs7LtclI9UdtGKM1gWTgtxFK0pIVdScVRfoQUp7QhjnG3YfXdCK8JLX1Qr9vPITxAi9nlzwqXMjbmA6AnhsuhiGkMIAWGLtYR774OztC7wtPn7dYj2MvWud-S3MuMXOmwg6gcXwfYyQ0gK45Vl3cHbWfcJt9sQ-xKmD6PGbqH-4Hh_d1OGdTlN0BmsLPhgdjfNh0A_RvTbr4NH5v0Rf3r39vP1QXH96f7V9fV0YQeRUSKgrxgQxrWCNkGAayWkjrTS1aJuSSqIrUouyogYE09oKaUhpeW03VErg_BK9OvmOczOANeCnqHs1RjfoeKuCdup_xLtO7cJB5fGS0jobPDsZHLVvtd-pfZijz5FVLokRUnJJGM205-c5MdzMkCY1uGSg7_OBw5xUKetNJotMJCeiiSGlCO2fLJSopfzFV-XyVS5fLeVnyZN_d_grOLedCU_Pnl3wuxuXUzbafGtdD4pxyut8RP4L1tu8Nw</recordid><startdate>20061014</startdate><enddate>20061014</enddate><creator>Calcagno, Danielle-Queiroz</creator><creator>Leal, Mariana-Ferreira</creator><creator>Seabra, Aline-Damaceno</creator><creator>Khayat, Andre-Salim</creator><creator>Chen, Elizabeth Suchi</creator><creator>Demachki, Samia</creator><creator>Assumpção, Paulo Pimentel</creator><creator>Faria, Mario Henrique Girão</creator><creator>Rabenhorst, Silvia Helena Barem</creator><creator>Ferreira, Márcia Valéria Pitombeira</creator><creator>de Arruda Cardoso Smith, Marília</creator><creator>Burbano, Rommel-Rodríguez</creator><general>Genetics Division, Department of Morphology, Federal University of S(a)o Paulo, S(a)o Paulo, SP, Brazil</general><general>Human Cytogenetics and Toxicological Genetics Laboratory, Department of Biology, Center of Biological Sciences, Federal University of Pará, Belém, PA, Brazil%Genetics Division, Department of Morphology, Federal University of S(a)o Paulo, S(a)o Paulo, SP, Brazil%Department of Pathology and Surgery Service,Federal University of Pará, Belém, PA, Brazil%Jo(a)o de Barros Barreto University Hospital, Federal University of Pará, Belém, PA, Brazil%Molecular Genetics Laboratory Department of Pathology, Medical School, Federal University of Ceará, Fortaleza, CE, Brazil%Human Cytogenetics and Toxicological Genetics Laboratory, Department of Biology, Center of Biological Sciences, Federal University of Pará, Belém, PA, Brazil</general><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><scope>5PM</scope></search><sort><creationdate>20061014</creationdate><title>Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma</title><author>Calcagno, Danielle-Queiroz ; Leal, Mariana-Ferreira ; Seabra, Aline-Damaceno ; Khayat, Andre-Salim ; Chen, Elizabeth Suchi ; Demachki, Samia ; Assumpção, Paulo Pimentel ; Faria, Mario Henrique Girão ; Rabenhorst, Silvia Helena Barem ; Ferreira, Márcia Valéria Pitombeira ; de Arruda Cardoso Smith, Marília ; Burbano, Rommel-Rodríguez</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-8e972240cf42b48ecb831b8d8c94fb6180a7094671ce42aad48c06d39d5188e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adult</topic><topic>Aged</topic><topic>Aneuploidy</topic><topic>Brazil</topic><topic>Chromosomes, Human, Pair 8</topic><topic>Gene Amplification</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes, myc</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Middle Aged</topic><topic>Rapid Communication</topic><topic>Stomach Neoplasms - genetics</topic><topic>基因表达</topic><topic>染色体</topic><topic>病理机制</topic><toplevel>online_resources</toplevel><creatorcontrib>Calcagno, Danielle-Queiroz</creatorcontrib><creatorcontrib>Leal, Mariana-Ferreira</creatorcontrib><creatorcontrib>Seabra, Aline-Damaceno</creatorcontrib><creatorcontrib>Khayat, Andre-Salim</creatorcontrib><creatorcontrib>Chen, Elizabeth Suchi</creatorcontrib><creatorcontrib>Demachki, Samia</creatorcontrib><creatorcontrib>Assumpção, Paulo Pimentel</creatorcontrib><creatorcontrib>Faria, Mario Henrique Girão</creatorcontrib><creatorcontrib>Rabenhorst, Silvia Helena Barem</creatorcontrib><creatorcontrib>Ferreira, Márcia Valéria Pitombeira</creatorcontrib><creatorcontrib>de Arruda Cardoso Smith, Marília</creatorcontrib><creatorcontrib>Burbano, Rommel-Rodríguez</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calcagno, Danielle-Queiroz</au><au>Leal, Mariana-Ferreira</au><au>Seabra, Aline-Damaceno</au><au>Khayat, Andre-Salim</au><au>Chen, Elizabeth Suchi</au><au>Demachki, Samia</au><au>Assumpção, Paulo Pimentel</au><au>Faria, Mario Henrique Girão</au><au>Rabenhorst, Silvia Helena Barem</au><au>Ferreira, Márcia Valéria Pitombeira</au><au>de Arruda Cardoso Smith, Marília</au><au>Burbano, Rommel-Rodríguez</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2006-10-14</date><risdate>2006</risdate><volume>12</volume><issue>38</issue><spage>6207</spage><epage>6211</epage><pages>6207-6211</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM: To investigate chromosome 8 numerical aberrations, C-MYC oncogene alterations and its expression in gastric cancer and to correlate these findings with histopathological characteristics of gastric tumors.
METHODS: Specimens were collected surgically from seven patients with gastric adenocarcinomas. Immunostaining for C-MYC and dual-color fluorescence in situ hybridization (FISH) for C-MYC gene and chromosome 8 centromere were performed.
RESULTS: All the cases showed chromosome 8 aneuploidy and C-MYC amplification, in both the diffuse and intestinal histopathological types of Lauren. No significant difference (P 〈 0.05) was observed between the level of chromosome 8 ploidy and the site, stage or histological type of the adenocarcinomas. C-MYC high amplification, like homogeneously stained regions (HSRs) and double minutes (DMs), was observed only in the intestinal-type. Structural rearrangement of C-MYC, like translocation, was observed only in the diffuse type. Regarding C-MYC gene, a significant difference (P 〈 0.05) was observed between the two histological types. The C-MYC protein was expressed in all the studied cases. In the intestinaltype the C-MYC immunoreactivity was localized only in the nucleus and in the diffuse type in the nucleus and cytoplasm.
CONCLUSION: Distinct patterns of alterations between intestinal and diffuse types of gastric tumors support the hypothesis that these types follow different genetic pathways.</abstract><cop>United States</cop><pub>Genetics Division, Department of Morphology, Federal University of S(a)o Paulo, S(a)o Paulo, SP, Brazil</pub><pmid>17036397</pmid><doi>10.3748/wjg.v12.i38.6207</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - genetics Adult Aged Aneuploidy Brazil Chromosomes, Human, Pair 8 Gene Amplification Gene Expression Regulation, Neoplastic Genes, myc Humans Immunohistochemistry In Situ Hybridization, Fluorescence Middle Aged Rapid Communication Stomach Neoplasms - genetics 基因表达 染色体 病理机制 |
title | Interrelationship between chromosome 8 aneuploidy, C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma |
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