Expression of isocitrate dehydrogenase-1 in glioblastoma, Bangladesh perspective

Ratim Mir, M. A. Islam, Nowfel Islam, M. N. Islam, Reba Das, Enamul Kabir
{"title":"Expression of isocitrate dehydrogenase-1 in glioblastoma, Bangladesh perspective","authors":"Ratim Mir, M. A. Islam, Nowfel Islam, M. N. Islam, Reba Das, Enamul Kabir","doi":"10.18203/2320-6012.ijrms20233977","DOIUrl":null,"url":null,"abstract":"Background: Glioblastoma is the most frequent malignant brain tumor in adults. Various studies have identified IDH (isocitrate dehydrogenase) mutation as a hallmark genetic alteration in glial tumors. The World Health Organization (WHO) has classified glioblastoma based on IDH mutation status, including IDH-mutant glioblastoma, IDH-wildtype glioblastoma along with its variants and glioblastoma, NOS (not otherwise specified) (where IDH mutation status cannot be evaluated). Methods: It was a cross-sectional observational study, conducted on 35 histologically diagnosed cases of glioblastoma, within the period of March, 2018 to December 2019. Results: Among the 35 glioblastoma cases, 6 (17.14%) were found to be IDH-mutant (positive for IDH1 immunostain), while the remaining 29 cases were negative for IDH1 immunostain (therefore designated as IDH-wildtype glioblastoma). In the IDH-mutant group, 3 out of 6 patients were in the younger age group (≤40 years). On the other hand, IDH-wildtype glioblastoma was more common in elderly and most frequent was in the age group of 51-60 years (11 out of 29 cases). Conclusions: In this study, IDH1 expression was observed in 17.14% of all glioblastoma cases (designated as IDH-mutant glioblastoma). Whereas, most (~82.86%) of the glioblastoma cases did not express IDH1 (designated as IDH-wildtype).","PeriodicalId":505944,"journal":{"name":"International Journal of Research in Medical Sciences","volume":"51 11","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Research in Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18203/2320-6012.ijrms20233977","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

Background: Glioblastoma is the most frequent malignant brain tumor in adults. Various studies have identified IDH (isocitrate dehydrogenase) mutation as a hallmark genetic alteration in glial tumors. The World Health Organization (WHO) has classified glioblastoma based on IDH mutation status, including IDH-mutant glioblastoma, IDH-wildtype glioblastoma along with its variants and glioblastoma, NOS (not otherwise specified) (where IDH mutation status cannot be evaluated). Methods: It was a cross-sectional observational study, conducted on 35 histologically diagnosed cases of glioblastoma, within the period of March, 2018 to December 2019. Results: Among the 35 glioblastoma cases, 6 (17.14%) were found to be IDH-mutant (positive for IDH1 immunostain), while the remaining 29 cases were negative for IDH1 immunostain (therefore designated as IDH-wildtype glioblastoma). In the IDH-mutant group, 3 out of 6 patients were in the younger age group (≤40 years). On the other hand, IDH-wildtype glioblastoma was more common in elderly and most frequent was in the age group of 51-60 years (11 out of 29 cases). Conclusions: In this study, IDH1 expression was observed in 17.14% of all glioblastoma cases (designated as IDH-mutant glioblastoma). Whereas, most (~82.86%) of the glioblastoma cases did not express IDH1 (designated as IDH-wildtype).
异柠檬酸脱氢酶-1 在胶质母细胞瘤中的表达,孟加拉国的视角
背景:胶质母细胞瘤是成人中最常见的恶性脑肿瘤。多项研究发现,IDH(异柠檬酸脱氢酶)突变是胶质瘤的标志性基因改变。世界卫生组织(WHO)根据IDH突变状态对胶质母细胞瘤进行了分类,包括IDH突变型胶质母细胞瘤、IDH野生型胶质母细胞瘤及其变异型和胶质母细胞瘤NOS(未另作规定)(无法评估IDH突变状态)。研究方法这是一项横断面观察性研究,在 2018 年 3 月至 2019 年 12 月期间对 35 例经组织学诊断的胶质母细胞瘤病例进行了研究。研究结果在35例胶质母细胞瘤病例中,发现6例(17.14%)为IDH突变型(IDH1免疫印迹阳性),其余29例为IDH1免疫印迹阴性(因此被称为IDH-野生型胶质母细胞瘤)。在 IDH 突变组中,6 例患者中有 3 例年龄较轻(≤40 岁)。另一方面,IDH-野生型胶质母细胞瘤多见于老年人,其中以 51-60 岁年龄组最多见(29 例中有 11 例)。结论在本研究中,17.14%的胶质母细胞瘤病例(被称为 IDH 突变型胶质母细胞瘤)有 IDH1 表达。而大多数(约 82.86%)胶质母细胞瘤病例不表达 IDH1(称为 IDH 野生型)。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信