Santiago Garfias-Arjona, Monica Lara-Almunia, Ester Antón-Valentí, Javier Pierola-Lopetegui, Joan Bestard-Escalas, Albert Maimó-Barceló, Diego M Marzese-Parrilli, Sandra Íñiguez-Muñoz, Miquel Ensenyat-Mendez, Marta Brell
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This study aimed to compare molecular factors of glioma samples with fluorescence intensity to identify potential cofounders and associations with clinically relevant tumor features.</p><p><strong>Methods: </strong>Tumor samples of high-grade glioma patients operated using 5-ALA for guided resection were included for comparative analysis of fluorescence intensity and molecular features. All the samples were processed under the same conditions. The power for fluorescent stimulation and acquisition time was the same between samples. An inverted fluorescence microscope compared the mean fluorescence for each molecular variation. p53, ATRX and Ki67 expression and IDH1 mutation were assessed by immunohistochemistry. Follow-up of the patients for progression-free survival and overall survival was made.</p><p><strong>Results: </strong>We found that the fluorescence intensity for each specific tumor was independent of the methylation of the methylguanine-DNA-methyltransferase (MGMT) promoter region assessed by pyrosequencing, there was no association of fluorescence with p53, ATRX, IDH1 mutation as assessed by immunochemistry. Also, fluorescence intensity has no relation with time of tumor recurrence or overall survival.</p><p><strong>Conclusion: </strong>With the results, we argue that many factors are involved in fluorescence intensity that may be related to the specific metabolic status of the glioma cells analyzed, which is more likely to be responsible for the variation of fluorescence.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"17 1","pages":"e77774"},"PeriodicalIF":1.0000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11749098/pdf/","citationCount":"0","resultStr":"{\"title\":\"Molecular Characteristics of High-Grade Glioma in Relation to 5-Aminolevulinic Acid (5-ALA) Fluorescence Intensity.\",\"authors\":\"Santiago Garfias-Arjona, Monica Lara-Almunia, Ester Antón-Valentí, Javier Pierola-Lopetegui, Joan Bestard-Escalas, Albert Maimó-Barceló, Diego M Marzese-Parrilli, Sandra Íñiguez-Muñoz, Miquel Ensenyat-Mendez, Marta Brell\",\"doi\":\"10.7759/cureus.77774\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>5-aminolevulinic acid (5-ALA) fluorescence used in glioma surgery has different intensities within tumors and among different patients, some molecular and external factors have been implicated, but there is no clear evidence analyzing the difference of fluorescence according to glioma molecular characteristics. 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Follow-up of the patients for progression-free survival and overall survival was made.</p><p><strong>Results: </strong>We found that the fluorescence intensity for each specific tumor was independent of the methylation of the methylguanine-DNA-methyltransferase (MGMT) promoter region assessed by pyrosequencing, there was no association of fluorescence with p53, ATRX, IDH1 mutation as assessed by immunochemistry. 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引用次数: 0
摘要
导语:胶质瘤手术中使用的5-氨基乙酰丙酸(5-ALA)荧光在肿瘤内和不同患者之间具有不同的强度,涉及一些分子和外部因素,但根据胶质瘤分子特征分析荧光的差异尚无明确的证据。本研究旨在比较胶质瘤样本的分子因子与荧光强度,以确定潜在的共同因素及其与临床相关肿瘤特征的关联。方法:采用5-ALA引导切除的高级别胶质瘤患者的肿瘤标本,比较分析其荧光强度和分子特征。所有样品均在相同条件下处理。不同样品的荧光刺激功率和采集时间相同。倒置荧光显微镜比较每个分子变异的平均荧光。免疫组化检测p53、ATRX、Ki67表达及IDH1突变。随访患者无进展生存期和总生存期。结果:我们发现每种肿瘤的荧光强度与甲基鸟嘌呤- dna -甲基转移酶(MGMT)启动子区的甲基化无关,与免疫化学评估的p53, ATRX, IDH1突变无关。荧光强度与肿瘤复发时间和总生存期无关。结论:我们认为荧光强度受多种因素影响,可能与所分析的胶质瘤细胞的特定代谢状态有关,更有可能是荧光变化的原因。
Molecular Characteristics of High-Grade Glioma in Relation to 5-Aminolevulinic Acid (5-ALA) Fluorescence Intensity.
Introduction: 5-aminolevulinic acid (5-ALA) fluorescence used in glioma surgery has different intensities within tumors and among different patients, some molecular and external factors have been implicated, but there is no clear evidence analyzing the difference of fluorescence according to glioma molecular characteristics. This study aimed to compare molecular factors of glioma samples with fluorescence intensity to identify potential cofounders and associations with clinically relevant tumor features.
Methods: Tumor samples of high-grade glioma patients operated using 5-ALA for guided resection were included for comparative analysis of fluorescence intensity and molecular features. All the samples were processed under the same conditions. The power for fluorescent stimulation and acquisition time was the same between samples. An inverted fluorescence microscope compared the mean fluorescence for each molecular variation. p53, ATRX and Ki67 expression and IDH1 mutation were assessed by immunohistochemistry. Follow-up of the patients for progression-free survival and overall survival was made.
Results: We found that the fluorescence intensity for each specific tumor was independent of the methylation of the methylguanine-DNA-methyltransferase (MGMT) promoter region assessed by pyrosequencing, there was no association of fluorescence with p53, ATRX, IDH1 mutation as assessed by immunochemistry. Also, fluorescence intensity has no relation with time of tumor recurrence or overall survival.
Conclusion: With the results, we argue that many factors are involved in fluorescence intensity that may be related to the specific metabolic status of the glioma cells analyzed, which is more likely to be responsible for the variation of fluorescence.