Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4229
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dc.contributor.authorBir, Ferda-
dc.contributor.authorÇallı-Demirkan, Neşe-
dc.contributor.authorTufan, A. Çevik-
dc.contributor.authorAkbulut, Metin-
dc.contributor.authorSatiroglu-Tufan, N. Lale-
dc.date.accessioned2019-08-16T11:32:56Z
dc.date.available2019-08-16T11:32:56Z
dc.date.issued2007-
dc.identifier.issn1007-9327-
dc.identifier.urihttps://hdl.handle.net/11499/4229-
dc.identifier.urihttps://doi.org/10.3748/wjg.v13.i23.3183-
dc.description.abstractAim: To investigate the apoptotic process of cells within the intestinal metaplasia areas co-localizing with chronic gastritis and gastric carcinomas and to analyze the involvement of proteins regulating apoptosis in the process of intestinal metaplasia related gastric carcinogenesis. Methods: Forty-two gastric carcinoma and seventeen chronic gastritis cases were included in this study. All cases were examined for the existence of intestinal metaplasia. Ten cases randomly selected from each group were processed for TUNEL assay. TUNEL positive cells within the intestinal metaplasia areas, colocalizing either to gastric carcinoma or chronic gastritis, were counted and converted to apoptotic indices. In addition, p53, bcl-2 and bax expression patterns within these tissues were analyzed on the basis of immunohistochemistry. Results: Twenty-eight of the cases were intestinal and 14 of the cases were diffuse type adenocarcinomas. 64% (27/42) of the gastric carcinoma cases had intestinal metaplasia. Intestinal metaplasia co-localized more with intestinal type carcinomas compared with diffuse type carcinomas [75% (21/28) vs 42% (6/14), respectively; P ? 0.05]. The mean apoptotic index in tumor cells was 0.70 ± 0.08. The mean apoptotic index in intestinal metaplasias co-localizing to tumors was significantly higher than that of intestinal metaplasias co-localizing to chronic gastritis (0.70 ± 0.03 vs 0.09 ± 0.01, respectively; P ? 0.05). p53 positivity was not observed in areas of intestinal metaplasia adjacent to tumors or chronic gastritis. Intestinal metaplasia areas adjacent to tumors showed lower cytoplasmic bcl-2 positivity compared to intestinal metaplasia areas adjacent to chronic gastritis [55.5% (15/27) vs 70.5% (12/17), respectively]. On the other hand, intestinal metaplasia areas adjacent to tumors showed significantly higher cytoplasmic bax positivity compared to intestinal metaplasia areas adjacent to chronic gastritis [44.4% (12/27) vs 11.7% (2/17), respectively; P ? 0.05]. Conclusion: Existence of apoptotic cells on the basis of TUNEL positivity is shown in intestinal metaplasias co-localizing to both diffuse and intestinal type gastric cancers in this study. Our results also suggested bax expression dependent induction of apoptosis especially in intestinal metaplasia areas adjacent to tumors. These findings strongly support the involvement of apoptotic mechanisms in the process of gastric carcinogenesis especially in the transition from intestinal metaplasia to gastric cancer. It may be suggested that induction of apoptosis in intestinal metaplasia areas adjacent to tumors may involve different mechanisms than induction by chronic inflammation. © 2007 The WJG Press. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherWJG Pressen_US
dc.relation.ispartofWorld Journal of Gastroenterologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectApoptosisen_US
dc.subjectBaxen_US
dc.subjectBcl-2en_US
dc.subjectGastric canceren_US
dc.subjectIntestinal metaplasiaen_US
dc.subjectp53en_US
dc.subjectTUNEL stainingen_US
dc.subjectprotein Baxen_US
dc.subjectprotein bcl 2en_US
dc.subjectprotein p53en_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectapoptosisen_US
dc.subjectarticleen_US
dc.subjectcancer classificationen_US
dc.subjectchronic gastritisen_US
dc.subjectcontrolled studyen_US
dc.subjectcytoplasmen_US
dc.subjectfemaleen_US
dc.subjectgastritisen_US
dc.subjecthistopathologyen_US
dc.subjecthumanen_US
dc.subjecthuman tissueen_US
dc.subjectimmunohistochemistryen_US
dc.subjectintestine metaplasiaen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmalignant transformationen_US
dc.subjectnick end labelingen_US
dc.subjectprotein analysisen_US
dc.subjectprotein expressionen_US
dc.subjectprotein functionen_US
dc.subjectregulatory mechanismen_US
dc.subjectstomach adenocarcinomaen_US
dc.subjectstomach carcinogenesisen_US
dc.subjectstomach carcinomaen_US
dc.subjecttissue distributionen_US
dc.titleApoptotic cell death and its relationship to gastric carcinogenesisen_US
dc.typeArticleen_US
dc.identifier.volume13en_US
dc.identifier.issue23en_US
dc.identifier.startpage3183
dc.identifier.startpage3183en_US
dc.identifier.endpage3188en_US
dc.authorid0000-0001-5860-100X-
dc.authorid0000-0002-5920-0475-
dc.authorid0000-0001-9399-0960-
dc.identifier.doi10.3748/wjg.v13.i23.3183-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid17589896en_US
dc.identifier.scopus2-s2.0-34447530415en_US
dc.identifier.wosWOS:000248546400006en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
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Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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