Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Brazil.
Department of Analytical Chemistry, Institute of Chemistry, Universidade Federal da Bahia (UFBA), Salvador, Brazil.
J Oral Pathol Med. 2019 Apr;48(4):307-314. doi: 10.1111/jop.12839. Epub 2019 Feb 28.
Ameloblastoma is a locally infiltrative, aggressive epithelial odontogenic neoplasm. BRAF-V600E mutation is frequently found in this tumor and has a pivotal role in its pathogenesis, but the consequences of this alteration need to be addressed. An untargeted metabolomics approach was applied to verify whether metabolic disturbances are related to tumor biology and whether BRAF-V600E mutation contributes to these alterations.
Formalin-fixed and paraffin-embedded tissue specimens from thirteen ameloblastoma and six dental follicles were included in this study. BRAF mutational status was determined by competitive allele-specific real-time PCR. Metabolite extracts were analyzed using gas chromatography coupled to mass spectrometry. Univariate and multivariate statistical methods were employed to compare the metabolic profiles of the samples.
The abundance of eleven metabolites was significantly higher in ameloblastoma in relation to dental follicles, including amino acids, fatty acids, carbohydrates, inorganic acids, and organoheterocyclic compounds. The presence of BRAF-V600E mutations in ameloblastoma was related to decreased levels of glycerol in comparison with tumors carrying only wild-type alleles of this gene. No metabolic differences were observed between recurrent and primary manifestations of ameloblastoma.
Ameloblastoma exhibits a distinct metabolic profile from normal odontogenic epithelium. BRAF-V600E may contribute to metabolic alterations in ameloblastoma. Collectively, our findings suggest that metabolic alterations might play a role in tumor pathogenesis.
成釉细胞瘤是一种局部浸润性、侵袭性的上皮性牙源性肿瘤。BRAF-V600E 突变在这种肿瘤中频繁发生,在其发病机制中起着关键作用,但需要阐明这种改变的后果。本研究采用非靶向代谢组学方法来验证代谢紊乱是否与肿瘤生物学相关,以及 BRAF-V600E 突变是否导致这些改变。
本研究纳入了 13 例成釉细胞瘤和 6 例牙滤泡的福尔马林固定石蜡包埋组织标本。通过竞争性等位基因特异性实时 PCR 确定 BRAF 突变状态。使用气相色谱-质谱联用分析代谢物提取物。采用单变量和多变量统计方法比较样本的代谢谱。
与牙滤泡相比,成釉细胞瘤中有 11 种代谢物的丰度明显升高,包括氨基酸、脂肪酸、碳水化合物、无机酸和杂环有机化合物。与仅携带 BRAF 基因野生型等位基因的肿瘤相比,成釉细胞瘤中存在 BRAF-V600E 突变与甘油水平降低相关。复发性和原发性成釉细胞瘤之间未观察到代谢差异。
成釉细胞瘤表现出与正常牙源性上皮不同的代谢特征。BRAF-V600E 可能导致成釉细胞瘤的代谢改变。总之,我们的研究结果表明,代谢改变可能在肿瘤发病机制中发挥作用。