Immunohistochemical Evaluation of p53 Expression and Proliferative Activity in Children with Helicobacter pylori Associated Gastritis
ABSTRACT Objectives: The aim of this study was to evaluate the significance of p53 expression and proliferative activity of glandular epithelium and intestinal metaplasia in Helicobacter pylori associated gastritis of pediatric patients. Methods: The study included endoscopic gastric biopsies of 54...
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Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 2005-04, Vol.40 (4), p.467-470 |
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creator | Ozturk, Yesim Ozer, Erdener Lebe, Banu Bekem, Ozlem Buyukgebiz, Benal |
description | ABSTRACT
Objectives:
The aim of this study was to evaluate the significance of p53 expression and proliferative activity of glandular epithelium and intestinal metaplasia in Helicobacter pylori associated gastritis of pediatric patients.
Methods:
The study included endoscopic gastric biopsies of 54 children with dyspeptic complaints. Immunohistochemistry was performed for evaluation of p53 expression and Ki‐67 labeling index, an indicator of proliferative activity. Grading of H. pylori density, intestinal metaplasia and inflammatory cell infiltration were performed in histologic tissue sections stained with hematoxylin‐eosin, Giemsa and Alcian‐blue.
Results:
Of 54 children, 35 (64%) were infected by H. pylori. Positive immunostaining for p53 was observed in 11 of 54 cases (20.4%). H. pylori infection was found in 10 (91%) of the p53‐positive patients. There was a positive correlation between H. pylori density and Ki‐67 labeling index in H. pylori infected children. H. pylori density, Ki‐67 labeling index and inflammatory cell infiltration in the p53‐positive group were significantly higher than in the p53‐negative group. Although intestinal metaplasia was more common in H. pylori infected children (n = 11; 31.4%), there was no difference in the rate of intestinal metaplasia between the p53‐positive and p53‐negative groups.
Conclusions:
The present study shows that p53 mutations and higher proliferative activity of glandular epithelium may be related to H. pylori associated gastritis in children. Because p53 mutation does not appear to be associated with intestinal metaplasia, a precursor for gastric cancer in adults, we think that H.pylori associated p53 alterations do not initiate and promote gastric cancer that may occur in adulthood. |
doi_str_mv | 10.1097/01.MPG.0000148832.22130.D7 |
format | Article |
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Objectives:
The aim of this study was to evaluate the significance of p53 expression and proliferative activity of glandular epithelium and intestinal metaplasia in Helicobacter pylori associated gastritis of pediatric patients.
Methods:
The study included endoscopic gastric biopsies of 54 children with dyspeptic complaints. Immunohistochemistry was performed for evaluation of p53 expression and Ki‐67 labeling index, an indicator of proliferative activity. Grading of H. pylori density, intestinal metaplasia and inflammatory cell infiltration were performed in histologic tissue sections stained with hematoxylin‐eosin, Giemsa and Alcian‐blue.
Results:
Of 54 children, 35 (64%) were infected by H. pylori. Positive immunostaining for p53 was observed in 11 of 54 cases (20.4%). H. pylori infection was found in 10 (91%) of the p53‐positive patients. There was a positive correlation between H. pylori density and Ki‐67 labeling index in H. pylori infected children. H. pylori density, Ki‐67 labeling index and inflammatory cell infiltration in the p53‐positive group were significantly higher than in the p53‐negative group. Although intestinal metaplasia was more common in H. pylori infected children (n = 11; 31.4%), there was no difference in the rate of intestinal metaplasia between the p53‐positive and p53‐negative groups.
Conclusions:
The present study shows that p53 mutations and higher proliferative activity of glandular epithelium may be related to H. pylori associated gastritis in children. Because p53 mutation does not appear to be associated with intestinal metaplasia, a precursor for gastric cancer in adults, we think that H.pylori associated p53 alterations do not initiate and promote gastric cancer that may occur in adulthood.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/01.MPG.0000148832.22130.D7</identifier><identifier>PMID: 15795596</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Adolescent ; Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Biological and medical sciences ; Child ; Child, Preschool ; Children‐p53 ; Female ; Gastric Mucosa - microbiology ; Gastric Mucosa - pathology ; Gastritis ; Gastritis - microbiology ; Gastritis - pathology ; Gastroenterology. Liver. Pancreas. Abdomen ; H. pylori ; Helicobacter Infections - pathology ; Helicobacter pylori ; Human bacterial diseases ; Humans ; Immunohistochemistry - methods ; Infectious diseases ; Intestines - pathology ; Ki-67 Antigen - chemistry ; Male ; Medical sciences ; Metaplasia ; Other diseases. Semiology ; Precancerous Conditions ; Proliferative activity‐Intestinal metaplasia ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2005-04, Vol.40 (4), p.467-470</ispartof><rights>2005 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>2005 Lippincott Williams & Wilkins, Inc.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5613-5ad75c8d79213e9ba8e041ae5edf513304f7c01bc9afe63f53d331d590bceb393</citedby><cites>FETCH-LOGICAL-c5613-5ad75c8d79213e9ba8e041ae5edf513304f7c01bc9afe63f53d331d590bceb393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2F01.MPG.0000148832.22130.D7$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2F01.MPG.0000148832.22130.D7$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16694151$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15795596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ozturk, Yesim</creatorcontrib><creatorcontrib>Ozer, Erdener</creatorcontrib><creatorcontrib>Lebe, Banu</creatorcontrib><creatorcontrib>Bekem, Ozlem</creatorcontrib><creatorcontrib>Buyukgebiz, Benal</creatorcontrib><title>Immunohistochemical Evaluation of p53 Expression and Proliferative Activity in Children with Helicobacter pylori Associated Gastritis</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>ABSTRACT
Objectives:
The aim of this study was to evaluate the significance of p53 expression and proliferative activity of glandular epithelium and intestinal metaplasia in Helicobacter pylori associated gastritis of pediatric patients.
Methods:
The study included endoscopic gastric biopsies of 54 children with dyspeptic complaints. Immunohistochemistry was performed for evaluation of p53 expression and Ki‐67 labeling index, an indicator of proliferative activity. Grading of H. pylori density, intestinal metaplasia and inflammatory cell infiltration were performed in histologic tissue sections stained with hematoxylin‐eosin, Giemsa and Alcian‐blue.
Results:
Of 54 children, 35 (64%) were infected by H. pylori. Positive immunostaining for p53 was observed in 11 of 54 cases (20.4%). H. pylori infection was found in 10 (91%) of the p53‐positive patients. There was a positive correlation between H. pylori density and Ki‐67 labeling index in H. pylori infected children. H. pylori density, Ki‐67 labeling index and inflammatory cell infiltration in the p53‐positive group were significantly higher than in the p53‐negative group. Although intestinal metaplasia was more common in H. pylori infected children (n = 11; 31.4%), there was no difference in the rate of intestinal metaplasia between the p53‐positive and p53‐negative groups.
Conclusions:
The present study shows that p53 mutations and higher proliferative activity of glandular epithelium may be related to H. pylori associated gastritis in children. Because p53 mutation does not appear to be associated with intestinal metaplasia, a precursor for gastric cancer in adults, we think that H.pylori associated p53 alterations do not initiate and promote gastric cancer that may occur in adulthood.</description><subject>Adolescent</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children‐p53</subject><subject>Female</subject><subject>Gastric Mucosa - microbiology</subject><subject>Gastric Mucosa - pathology</subject><subject>Gastritis</subject><subject>Gastritis - microbiology</subject><subject>Gastritis - pathology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>H. pylori</subject><subject>Helicobacter Infections - pathology</subject><subject>Helicobacter pylori</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Infectious diseases</subject><subject>Intestines - pathology</subject><subject>Ki-67 Antigen - chemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metaplasia</subject><subject>Other diseases. Semiology</subject><subject>Precancerous Conditions</subject><subject>Proliferative activity‐Intestinal metaplasia</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkcGO0zAQhi0EYkvhFZCFBLcEO47jhFvpdruLFugBzpbjTBSDE3ftZEsfgPfG3UbqGV9Gtr7f_8z8CL2jJKWkEh8JTb_utimJh-ZlybI0yygj6bV4hhaUsyLJS0KfowXJhEgySosr9CqEX5EXOScv0RXlouK8Khbo713fT4PrTBid7qA3Wlm8eVR2UqNxA3Yt3nOGN3_2HkI4vaihwTvvrGnBR-YR8ErHYsYjNgNed8Y2HgZ8MGOHb8Ea7WqlR_B4f7TOG7wKwWmjRmjwVoXRm9GE1-hFq2yAN3Ndop83mx_r2-T--_ZuvbpPNC8oS7hqBNdlI6o4L1S1KoHkVAGHpuWUMZK3QhNa60q1ULCWs4Yx2vCK1BpqVrEl-nD-d-_dwwRhlL0JGqxVA7gpyEJEHyJIBD-dQe1dCB5aufemV_4oKZGnECShMoYgLyHIpxDktYjit7PLVPfQXKTz1iPwfgZUiPtuvRq0CReuKKqcxoGWKD9zB2fjBsNvOx3Ayw6UHbsna05FkWSxkjzeklMzLMrWs8xYOP5H5_LL7hv7fEMYITn7BxLQteQ</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Ozturk, Yesim</creator><creator>Ozer, Erdener</creator><creator>Lebe, Banu</creator><creator>Bekem, Ozlem</creator><creator>Buyukgebiz, Benal</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott</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>7X8</scope></search><sort><creationdate>200504</creationdate><title>Immunohistochemical Evaluation of p53 Expression and Proliferative Activity in Children with Helicobacter pylori Associated Gastritis</title><author>Ozturk, Yesim ; Ozer, Erdener ; Lebe, Banu ; Bekem, Ozlem ; Buyukgebiz, Benal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5613-5ad75c8d79213e9ba8e041ae5edf513304f7c01bc9afe63f53d331d590bceb393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children‐p53</topic><topic>Female</topic><topic>Gastric Mucosa - microbiology</topic><topic>Gastric Mucosa - pathology</topic><topic>Gastritis</topic><topic>Gastritis - microbiology</topic><topic>Gastritis - pathology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>H. pylori</topic><topic>Helicobacter Infections - pathology</topic><topic>Helicobacter pylori</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Immunohistochemistry - methods</topic><topic>Infectious diseases</topic><topic>Intestines - pathology</topic><topic>Ki-67 Antigen - chemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metaplasia</topic><topic>Other diseases. Semiology</topic><topic>Precancerous Conditions</topic><topic>Proliferative activity‐Intestinal metaplasia</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozturk, Yesim</creatorcontrib><creatorcontrib>Ozer, Erdener</creatorcontrib><creatorcontrib>Lebe, Banu</creatorcontrib><creatorcontrib>Bekem, Ozlem</creatorcontrib><creatorcontrib>Buyukgebiz, Benal</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>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozturk, Yesim</au><au>Ozer, Erdener</au><au>Lebe, Banu</au><au>Bekem, Ozlem</au><au>Buyukgebiz, Benal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical Evaluation of p53 Expression and Proliferative Activity in Children with Helicobacter pylori Associated Gastritis</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2005-04</date><risdate>2005</risdate><volume>40</volume><issue>4</issue><spage>467</spage><epage>470</epage><pages>467-470</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>ABSTRACT
Objectives:
The aim of this study was to evaluate the significance of p53 expression and proliferative activity of glandular epithelium and intestinal metaplasia in Helicobacter pylori associated gastritis of pediatric patients.
Methods:
The study included endoscopic gastric biopsies of 54 children with dyspeptic complaints. Immunohistochemistry was performed for evaluation of p53 expression and Ki‐67 labeling index, an indicator of proliferative activity. Grading of H. pylori density, intestinal metaplasia and inflammatory cell infiltration were performed in histologic tissue sections stained with hematoxylin‐eosin, Giemsa and Alcian‐blue.
Results:
Of 54 children, 35 (64%) were infected by H. pylori. Positive immunostaining for p53 was observed in 11 of 54 cases (20.4%). H. pylori infection was found in 10 (91%) of the p53‐positive patients. There was a positive correlation between H. pylori density and Ki‐67 labeling index in H. pylori infected children. H. pylori density, Ki‐67 labeling index and inflammatory cell infiltration in the p53‐positive group were significantly higher than in the p53‐negative group. Although intestinal metaplasia was more common in H. pylori infected children (n = 11; 31.4%), there was no difference in the rate of intestinal metaplasia between the p53‐positive and p53‐negative groups.
Conclusions:
The present study shows that p53 mutations and higher proliferative activity of glandular epithelium may be related to H. pylori associated gastritis in children. Because p53 mutation does not appear to be associated with intestinal metaplasia, a precursor for gastric cancer in adults, we think that H.pylori associated p53 alterations do not initiate and promote gastric cancer that may occur in adulthood.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>15795596</pmid><doi>10.1097/01.MPG.0000148832.22130.D7</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Bacterial diseases Bacterial diseases of the digestive system and abdomen Biological and medical sciences Child Child, Preschool Children‐p53 Female Gastric Mucosa - microbiology Gastric Mucosa - pathology Gastritis Gastritis - microbiology Gastritis - pathology Gastroenterology. Liver. Pancreas. Abdomen H. pylori Helicobacter Infections - pathology Helicobacter pylori Human bacterial diseases Humans Immunohistochemistry - methods Infectious diseases Intestines - pathology Ki-67 Antigen - chemistry Male Medical sciences Metaplasia Other diseases. Semiology Precancerous Conditions Proliferative activity‐Intestinal metaplasia Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumor Suppressor Protein p53 - metabolism |
title | Immunohistochemical Evaluation of p53 Expression and Proliferative Activity in Children with Helicobacter pylori Associated Gastritis |
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