Clinicopathological and immunohistochemical analysis of gastrointestinal stromal tumor
AIM: To investigate the clinicopathological features of gastrointestinal stromal tumor (GIST) and to study the reference indexes for malignancy. METHODS: Fifty-two cases of primary GIST were distinguished from a group of gastrointestinal mesenchymal tumors using a panel of antibodies such as CD117 a...
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description | AIM: To investigate the clinicopathological features of gastrointestinal stromal tumor (GIST) and to study the reference indexes for malignancy. METHODS: Fifty-two cases of primary GIST were distinguished from a group of gastrointestinal mesenchymal tumors using a panel of antibodies such as CD117 and CD34 by immunohistochemical SP method. Their biological behaviors were analyzed using the expression of p21WAF1 and Bax in 52 cases of GIST. RESULTS: Grossly, the tumor size was between 1.5 cm and 13 cm (mean: 5.5 cm). Focal areas of hemorrhage, necrosis, or small cyst formation could be seen. Microscopically, the tumor was composed of spindle cells (20 cases), epithelioid cells (20 cases) and mixed cells (12 cases). Immunohistochemically, CDl17 and CD34 showed diffuse strong positive expressions, the positive rates were 98.1% and 92.3%. SMA, S-100, NSE, NF and MBP showed focal positive expressions, the positive rates were 48.1%, 28.8%, 25%, 21.2% and 42.3% respectively. Vimentins were all positive desmin and CgA were all negative. In normal adult stomach and intestine, the immunoreactive staining for CD117 and CD34 showed immunoreactive interstitial cells of Cajal in myenteric neuroplexus. Among the 52 cases of GIST, 27 were positive for p21WAF1 (51.9%), 29 for Bax (55.8%). The expression of p21WAF1 and Bax had no significent difference with the localization, size, histological subtype of GIST, but had a significent difference with the histological grade (P = 0.000, respectively), p21WAF1 expression had a positive correlation to Bax expression (r = 0.461, P = 0.001, k = 0.459). CONCLUSION: GIST has complicated arrangements and various cell types. Positivity of CD117 and CD34 is the most valuable factor in diagnosing GIST. Expression of p21WAF1 and Bax plays an important role in potential malignancy and malignancy rather than in benign GIST. p21WAF1 and Bax may be used as the markers in the assessment of GIST malignant potential. |
doi_str_mv | 10.3748/wjg.v12.i26.4161 |
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METHODS: Fifty-two cases of primary GIST were distinguished from a group of gastrointestinal mesenchymal tumors using a panel of antibodies such as CD117 and CD34 by immunohistochemical SP method. Their biological behaviors were analyzed using the expression of p21WAF1 and Bax in 52 cases of GIST. RESULTS: Grossly, the tumor size was between 1.5 cm and 13 cm (mean: 5.5 cm). Focal areas of hemorrhage, necrosis, or small cyst formation could be seen. Microscopically, the tumor was composed of spindle cells (20 cases), epithelioid cells (20 cases) and mixed cells (12 cases). Immunohistochemically, CDl17 and CD34 showed diffuse strong positive expressions, the positive rates were 98.1% and 92.3%. SMA, S-100, NSE, NF and MBP showed focal positive expressions, the positive rates were 48.1%, 28.8%, 25%, 21.2% and 42.3% respectively. Vimentins were all positive desmin and CgA were all negative. In normal adult stomach and intestine, the immunoreactive staining for CD117 and CD34 showed immunoreactive interstitial cells of Cajal in myenteric neuroplexus. Among the 52 cases of GIST, 27 were positive for p21WAF1 (51.9%), 29 for Bax (55.8%). The expression of p21WAF1 and Bax had no significent difference with the localization, size, histological subtype of GIST, but had a significent difference with the histological grade (P = 0.000, respectively), p21WAF1 expression had a positive correlation to Bax expression (r = 0.461, P = 0.001, k = 0.459). CONCLUSION: GIST has complicated arrangements and various cell types. Positivity of CD117 and CD34 is the most valuable factor in diagnosing GIST. Expression of p21WAF1 and Bax plays an important role in potential malignancy and malignancy rather than in benign GIST. p21WAF1 and Bax may be used as the markers in the assessment of GIST malignant potential.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v12.i26.4161</identifier><identifier>PMID: 16830365</identifier><language>eng</language><publisher>United States: Department of Research, Harbin Medical University, Harbin 150086, Heilongjiang Province, China%Department of Pathology, First Hospital of Harbin Medical University, Harbin 150001, Heilong jiang Province, China</publisher><subject>Adult ; Aged ; Antigens, CD34 - genetics ; Antigens, CD34 - metabolism ; Basic Research ; bcl-2-Associated X Protein - genetics ; bcl-2-Associated X Protein - metabolism ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cyclin-Dependent Kinase Inhibitor p21 - genetics ; Cyclin-Dependent Kinase Inhibitor p21 - metabolism ; Gastrointestinal Stromal Tumors - diagnosis ; Gastrointestinal Stromal Tumors - genetics ; Gastrointestinal Stromal Tumors - metabolism ; Gastrointestinal Stromal Tumors - pathology ; Gene Expression Regulation, Neoplastic ; Genetic Markers ; Humans ; Immunohistochemistry ; Middle Aged ; Prognosis ; Proto-Oncogene Proteins c-kit - genetics ; Proto-Oncogene Proteins c-kit - metabolism ; 临床病理学 ; 免疫组织化学的 ; 胃肠基质肿瘤</subject><ispartof>World journal of gastroenterology : WJG, 2006-07, Vol.12 (26), p.4161-4165</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-c516t-16676d42f5a9afdf22f9fd9002e460efa9acbde79899d3e1bbf736560d9459f23</citedby><cites>FETCH-LOGICAL-c516t-16676d42f5a9afdf22f9fd9002e460efa9acbde79899d3e1bbf736560d9459f23</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/PMC4087364/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4087364/$$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/16830365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Feng-Yu</creatorcontrib><creatorcontrib>Qi, Ji-Ping</creatorcontrib><creatorcontrib>Xu, Feng-Lin</creatorcontrib><creatorcontrib>Wu, Ai-Ping</creatorcontrib><title>Clinicopathological and immunohistochemical analysis of gastrointestinal stromal tumor</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To investigate the clinicopathological features of gastrointestinal stromal tumor (GIST) and to study the reference indexes for malignancy. METHODS: Fifty-two cases of primary GIST were distinguished from a group of gastrointestinal mesenchymal tumors using a panel of antibodies such as CD117 and CD34 by immunohistochemical SP method. Their biological behaviors were analyzed using the expression of p21WAF1 and Bax in 52 cases of GIST. RESULTS: Grossly, the tumor size was between 1.5 cm and 13 cm (mean: 5.5 cm). Focal areas of hemorrhage, necrosis, or small cyst formation could be seen. Microscopically, the tumor was composed of spindle cells (20 cases), epithelioid cells (20 cases) and mixed cells (12 cases). Immunohistochemically, CDl17 and CD34 showed diffuse strong positive expressions, the positive rates were 98.1% and 92.3%. SMA, S-100, NSE, NF and MBP showed focal positive expressions, the positive rates were 48.1%, 28.8%, 25%, 21.2% and 42.3% respectively. Vimentins were all positive desmin and CgA were all negative. In normal adult stomach and intestine, the immunoreactive staining for CD117 and CD34 showed immunoreactive interstitial cells of Cajal in myenteric neuroplexus. Among the 52 cases of GIST, 27 were positive for p21WAF1 (51.9%), 29 for Bax (55.8%). The expression of p21WAF1 and Bax had no significent difference with the localization, size, histological subtype of GIST, but had a significent difference with the histological grade (P = 0.000, respectively), p21WAF1 expression had a positive correlation to Bax expression (r = 0.461, P = 0.001, k = 0.459). CONCLUSION: GIST has complicated arrangements and various cell types. Positivity of CD117 and CD34 is the most valuable factor in diagnosing GIST. Expression of p21WAF1 and Bax plays an important role in potential malignancy and malignancy rather than in benign GIST. p21WAF1 and Bax may be used as the markers in the assessment of GIST malignant potential.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigens, CD34 - genetics</subject><subject>Antigens, CD34 - metabolism</subject><subject>Basic Research</subject><subject>bcl-2-Associated X Protein - genetics</subject><subject>bcl-2-Associated X Protein - metabolism</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - genetics</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</subject><subject>Gastrointestinal Stromal Tumors - diagnosis</subject><subject>Gastrointestinal Stromal Tumors - genetics</subject><subject>Gastrointestinal Stromal Tumors - metabolism</subject><subject>Gastrointestinal Stromal Tumors - pathology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetic Markers</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Proto-Oncogene Proteins c-kit - genetics</subject><subject>Proto-Oncogene Proteins c-kit - metabolism</subject><subject>临床病理学</subject><subject>免疫组织化学的</subject><subject>胃肠基质肿瘤</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>eNpVUcuO1DAQtBCIHRbunFCEELcMfsWJL0hoxEtaiQtwtRzHTjw49qyd7Gr_nh5NxOPUcru6uqoLoZcE71nLu3f3x3F_R-jeU7HnRJBHaEcpkTXtOH6MdgTjtpaMtlfoWSlHjCljDX2KrojoGGai2aGfh-CjN-mklymFNHqjQ6XjUPl5XmOafFmSmey89XV4KL5UyVWjLktOPi62LB761fk5Q13WOeXn6InTodgXW71GPz59_H74Ut98-_z18OGmNg0RS02EaMXAqWu01G5wlDrpBglCLRfYOuiafrCt7KQcmCV971qQLfAgeSMdZdfo_YX3tPazHYyNS9ZBnbKfdX5QSXv1_0_0kxrTneK4AyYOBG8uBPc6Oh1HdUxrBjtFwW0pxoIKOCLA3m57crpdwbKafTE2BB1tWosSnQAvjQAgvgBNTqVk6_5oIVidMzvzKshMQWbqnBmMvPrXw9-BLSQAvN44pxTHWw8qe21-OR-sopRTKnjLfgMS1qJw</recordid><startdate>20060714</startdate><enddate>20060714</enddate><creator>Liu, Feng-Yu</creator><creator>Qi, Ji-Ping</creator><creator>Xu, Feng-Lin</creator><creator>Wu, Ai-Ping</creator><general>Department of Research, Harbin Medical University, Harbin 150086, Heilongjiang Province, China%Department of Pathology, First Hospital of Harbin Medical University, Harbin 150001, Heilong jiang Province, China</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>20060714</creationdate><title>Clinicopathological and immunohistochemical analysis of gastrointestinal stromal tumor</title><author>Liu, Feng-Yu ; Qi, Ji-Ping ; Xu, Feng-Lin ; Wu, Ai-Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-16676d42f5a9afdf22f9fd9002e460efa9acbde79899d3e1bbf736560d9459f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigens, CD34 - genetics</topic><topic>Antigens, CD34 - metabolism</topic><topic>Basic Research</topic><topic>bcl-2-Associated X Protein - genetics</topic><topic>bcl-2-Associated X Protein - metabolism</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - genetics</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</topic><topic>Gastrointestinal Stromal Tumors - diagnosis</topic><topic>Gastrointestinal Stromal Tumors - genetics</topic><topic>Gastrointestinal Stromal Tumors - metabolism</topic><topic>Gastrointestinal Stromal Tumors - pathology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetic Markers</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Proto-Oncogene Proteins c-kit - genetics</topic><topic>Proto-Oncogene Proteins c-kit - metabolism</topic><topic>临床病理学</topic><topic>免疫组织化学的</topic><topic>胃肠基质肿瘤</topic><toplevel>online_resources</toplevel><creatorcontrib>Liu, Feng-Yu</creatorcontrib><creatorcontrib>Qi, Ji-Ping</creatorcontrib><creatorcontrib>Xu, Feng-Lin</creatorcontrib><creatorcontrib>Wu, Ai-Ping</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>Liu, Feng-Yu</au><au>Qi, Ji-Ping</au><au>Xu, Feng-Lin</au><au>Wu, Ai-Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinicopathological and immunohistochemical analysis of gastrointestinal stromal tumor</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2006-07-14</date><risdate>2006</risdate><volume>12</volume><issue>26</issue><spage>4161</spage><epage>4165</epage><pages>4161-4165</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM: To investigate the clinicopathological features of gastrointestinal stromal tumor (GIST) and to study the reference indexes for malignancy. METHODS: Fifty-two cases of primary GIST were distinguished from a group of gastrointestinal mesenchymal tumors using a panel of antibodies such as CD117 and CD34 by immunohistochemical SP method. Their biological behaviors were analyzed using the expression of p21WAF1 and Bax in 52 cases of GIST. RESULTS: Grossly, the tumor size was between 1.5 cm and 13 cm (mean: 5.5 cm). Focal areas of hemorrhage, necrosis, or small cyst formation could be seen. Microscopically, the tumor was composed of spindle cells (20 cases), epithelioid cells (20 cases) and mixed cells (12 cases). Immunohistochemically, CDl17 and CD34 showed diffuse strong positive expressions, the positive rates were 98.1% and 92.3%. SMA, S-100, NSE, NF and MBP showed focal positive expressions, the positive rates were 48.1%, 28.8%, 25%, 21.2% and 42.3% respectively. Vimentins were all positive desmin and CgA were all negative. In normal adult stomach and intestine, the immunoreactive staining for CD117 and CD34 showed immunoreactive interstitial cells of Cajal in myenteric neuroplexus. Among the 52 cases of GIST, 27 were positive for p21WAF1 (51.9%), 29 for Bax (55.8%). The expression of p21WAF1 and Bax had no significent difference with the localization, size, histological subtype of GIST, but had a significent difference with the histological grade (P = 0.000, respectively), p21WAF1 expression had a positive correlation to Bax expression (r = 0.461, P = 0.001, k = 0.459). CONCLUSION: GIST has complicated arrangements and various cell types. Positivity of CD117 and CD34 is the most valuable factor in diagnosing GIST. Expression of p21WAF1 and Bax plays an important role in potential malignancy and malignancy rather than in benign GIST. p21WAF1 and Bax may be used as the markers in the assessment of GIST malignant potential.</abstract><cop>United States</cop><pub>Department of Research, Harbin Medical University, Harbin 150086, Heilongjiang Province, China%Department of Pathology, First Hospital of Harbin Medical University, Harbin 150001, Heilong jiang Province, China</pub><pmid>16830365</pmid><doi>10.3748/wjg.v12.i26.4161</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antigens, CD34 - genetics Antigens, CD34 - metabolism Basic Research bcl-2-Associated X Protein - genetics bcl-2-Associated X Protein - metabolism Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Cyclin-Dependent Kinase Inhibitor p21 - genetics Cyclin-Dependent Kinase Inhibitor p21 - metabolism Gastrointestinal Stromal Tumors - diagnosis Gastrointestinal Stromal Tumors - genetics Gastrointestinal Stromal Tumors - metabolism Gastrointestinal Stromal Tumors - pathology Gene Expression Regulation, Neoplastic Genetic Markers Humans Immunohistochemistry Middle Aged Prognosis Proto-Oncogene Proteins c-kit - genetics Proto-Oncogene Proteins c-kit - metabolism 临床病理学 免疫组织化学的 胃肠基质肿瘤 |
title | Clinicopathological and immunohistochemical analysis of gastrointestinal stromal tumor |
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