The Evaluation of Wnt Pathway Proteins (Wnt-1/Β-Catenin/ E-Cadherin) in Bone Marrow Biopsies in Essential Thrombocythemia and Polycythemia Vera

H. Kucuk, U. Cobanoglu, M. Sonmez
{"title":"The Evaluation of Wnt Pathway Proteins (Wnt-1/Β-Catenin/ E-Cadherin) in Bone Marrow Biopsies in Essential Thrombocythemia and Polycythemia Vera","authors":"H. Kucuk, U. Cobanoglu, M. Sonmez","doi":"10.7176/jstr/7-06-04","DOIUrl":null,"url":null,"abstract":"The aim of the study is to investigate the expressions of Wnt signal pathway proteins (Wnt 1/Β Catenin/E Cadherin) in polycythemia vera and essential thrombocythemia. In addition to 25 Polycythemia vera and 25 Essential thrombocytosis cases who received bone marrow biopsies with the diagnoses of Polycythemia vera and Essential thrombocytosis, 25 normocellular bone marrow biopsies were included as the control group. In cells belonging to erythroid, myeloid and megakaryocytic series in the bone marrow biopsies of the cases, Wnt 1, β catenin and E cadherin expressions were examined by the immunohistochemical method. For each series, staining up to 10% was accepted as negative, and 10% and higher staining was accepted as positive. In the Essential thrombocytosis cases, there was a significant increase in the Wnt 1 expression in the megakaryocytic series and E cadherin expression in the erythroid series (p<0.05). When the cases were assessed within themselves based on the three series, an increase in E cadherin and E cadherin expression in the erythroid series in the Polycythemia vera cases and Wnt 1 expression in the megakaryocytic series in the Essential thrombocytosis cases was observed (p<0.05). β catenin expression was not encountered in the cases. Consequently, it was considered that Wnt 1 may be associated with megakaryocytopoiesis in ET cases, and E cadherin may be associated with erythropoiesis in ET cases. However, it will be beneficial to repeat the study on broader myeloproliferative neoplasm series and assess other factors in the Wnt pathway. Keywords: Essential Thrombocytosis, Polycythemia Vera, Wnt 1, β catenin, E cadherin DOI: 10.7176/JSTR/7-06-04","PeriodicalId":14256,"journal":{"name":"International Journal of Scientific and Technological Research","volume":"32 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Scientific and Technological Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7176/jstr/7-06-04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The aim of the study is to investigate the expressions of Wnt signal pathway proteins (Wnt 1/Β Catenin/E Cadherin) in polycythemia vera and essential thrombocythemia. In addition to 25 Polycythemia vera and 25 Essential thrombocytosis cases who received bone marrow biopsies with the diagnoses of Polycythemia vera and Essential thrombocytosis, 25 normocellular bone marrow biopsies were included as the control group. In cells belonging to erythroid, myeloid and megakaryocytic series in the bone marrow biopsies of the cases, Wnt 1, β catenin and E cadherin expressions were examined by the immunohistochemical method. For each series, staining up to 10% was accepted as negative, and 10% and higher staining was accepted as positive. In the Essential thrombocytosis cases, there was a significant increase in the Wnt 1 expression in the megakaryocytic series and E cadherin expression in the erythroid series (p<0.05). When the cases were assessed within themselves based on the three series, an increase in E cadherin and E cadherin expression in the erythroid series in the Polycythemia vera cases and Wnt 1 expression in the megakaryocytic series in the Essential thrombocytosis cases was observed (p<0.05). β catenin expression was not encountered in the cases. Consequently, it was considered that Wnt 1 may be associated with megakaryocytopoiesis in ET cases, and E cadherin may be associated with erythropoiesis in ET cases. However, it will be beneficial to repeat the study on broader myeloproliferative neoplasm series and assess other factors in the Wnt pathway. Keywords: Essential Thrombocytosis, Polycythemia Vera, Wnt 1, β catenin, E cadherin DOI: 10.7176/JSTR/7-06-04
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
原发性血小板增多症和真性红细胞增多症患者骨髓活检中Wnt通路蛋白(Wnt-1/Β-Catenin/ E-Cadherin)的评价
本研究旨在探讨Wnt信号通路蛋白(Wnt 1/Β Catenin/E Cadherin)在真性红细胞增多症和原发性血小板增多症中的表达。除25例真性红细胞增多症和25例原发性血小板增多症患者行骨髓活检诊断为真性红细胞增多症和原发性血小板增多症外,25例正常细胞骨髓活检为对照组。采用免疫组化方法检测患者骨髓活检属红系、髓系和巨核系细胞Wnt 1、β catenin和E cadherin的表达。对于每个系列,高达10%的染色被接受为阴性,10%及以上的染色被接受为阳性。在原发性血小板增多病例中,巨核系Wnt 1表达显著升高,红细胞系E cadherin表达显著升高(p<0.05)。在三个系列的基础上进行内部评估时,真性红细胞增多症患者红系E - cadherin和E - cadherin表达升高,原发性血小板增多症患者巨核细胞系Wnt - 1表达升高(p<0.05)。未见β连环蛋白表达。因此,我们认为Wnt 1可能与ET病例中的巨核细胞生成有关,E钙粘蛋白可能与ET病例中的红细胞生成有关。然而,在更广泛的骨髓增殖性肿瘤系列中重复研究并评估Wnt通路中的其他因素将是有益的。关键词:原发性血小板增多症,真性红细胞增多症,Wnt 1, β catenin, E cadherin
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Studies on Marine Pollution Caused By Litters in the Marmara Sea on the Coast of Turkey The Relationship between Protein Consumption and Abdominal Obesity An Analysis of the Studies on Self-Efficacy in Mathematics Education in Turkey Restorative Dental Treatment Approach on an Anorexia Nervosa Patient: A Case Report The Effect of Insemination Time, Season and Insemination Method on Calf Gender in Holstein Cattle
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1