中国实用神经疾病杂志
中國實用神經疾病雜誌
중국실용신경질병잡지
CHINESE JOURNAL OF PRACTICAL NERVOUS DISEASES
2014年
11期
45-47
,共3页
神经胶质瘤%IDH1%NS%基因突变
神經膠質瘤%IDH1%NS%基因突變
신경효질류%IDH1%NS%기인돌변
Glioma%IDH1%NS%Mutation of gene
目的:分析胶质瘤中核干细胞因子(NS)表达和异柠檬酸脱氢酶1(IDHI)基因突变的特点,为胶质瘤的诊断、治疗提供理论依据。方法对58例原发性胶质瘤存档蜡块分析,采用免疫组织化学法检测 NS 蛋白的表达情况,应用 PCR技术检测标本中IDH1基因多态性变化。结果免疫组织化学法检测显示,在高级别胶质瘤标本中NS蛋白表达率高于低级别。经基因直接测序,16例(55.2%)出现IDH1突变,突变位点均为R132型。经统计学分析,IDH1基因突变率与胶质瘤病理分级呈正相关。结论在胶质瘤中核干细胞因子表达和ID H l基因突变率随病理级别的增加而增加,可为胶质瘤的诊断提供有力的证据,并为胶质瘤在基因治疗方面指出了新的研究方向。
目的:分析膠質瘤中覈榦細胞因子(NS)錶達和異檸檬痠脫氫酶1(IDHI)基因突變的特點,為膠質瘤的診斷、治療提供理論依據。方法對58例原髮性膠質瘤存檔蠟塊分析,採用免疫組織化學法檢測 NS 蛋白的錶達情況,應用 PCR技術檢測標本中IDH1基因多態性變化。結果免疫組織化學法檢測顯示,在高級彆膠質瘤標本中NS蛋白錶達率高于低級彆。經基因直接測序,16例(55.2%)齣現IDH1突變,突變位點均為R132型。經統計學分析,IDH1基因突變率與膠質瘤病理分級呈正相關。結論在膠質瘤中覈榦細胞因子錶達和ID H l基因突變率隨病理級彆的增加而增加,可為膠質瘤的診斷提供有力的證據,併為膠質瘤在基因治療方麵指齣瞭新的研究方嚮。
목적:분석효질류중핵간세포인자(NS)표체화이저몽산탈경매1(IDHI)기인돌변적특점,위효질류적진단、치료제공이론의거。방법대58례원발성효질류존당사괴분석,채용면역조직화학법검측 NS 단백적표체정황,응용 PCR기술검측표본중IDH1기인다태성변화。결과면역조직화학법검측현시,재고급별효질류표본중NS단백표체솔고우저급별。경기인직접측서,16례(55.2%)출현IDH1돌변,돌변위점균위R132형。경통계학분석,IDH1기인돌변솔여효질류병리분급정정상관。결론재효질류중핵간세포인자표체화ID H l기인돌변솔수병리급별적증가이증가,가위효질류적진단제공유력적증거,병위효질류재기인치료방면지출료신적연구방향。
Objective To analyze the characteristic of expression of NS and isocitrate dehydrogenase (IDH1) gene muta-tions in gliomas ,as to provide theoretical basis for the diagnosis and treatment of glioma. Methods Fifty-eight human glioma samples were analyzed. The protein expression levels of NS were measured by IHC. The polymorphisms change of IDH1 gene was detected by real-time quantitative PCR.Results Upshots immuno-histochemistry manifested that the positive expression rate of NS in high level gloma tissue was higher than that in low level glioma. Gene sequencing manifested that IDH1 gene mu-tations were observed in 16 samples having gliomas(55.2% ) ,and the mutation appeared as R132H type. By the SPSS analy-sis ,IDH1 gene mutation rate had a certain correlation with glioma pathology classification.Conclusion As the increase of path-ological level ,the expression of NS and IDH1 gene mutations rate are increased in glioma. It can provide strong evidence for the diagnosis of glioma and opened up a new research way in gene therapy for gliomas.