期刊论文详细信息
Journal of Nuclear Medicine
Relationship Between 18F-FDG Accumulation and Lactate Dehydrogenase A Expression in Lung Adenocarcinomas
Gang Huang1  Xiang Zhou1  Jianjun Liu1  Ruohua Chen1  Wenhui Xie1  Yicheng Ni1 
关键词: lung adenocarcinomas;    LDHA;    GLUT1;    glycolysis;    18F-FDG uptake;   
DOI  :  10.2967/jnumed.114.145490
学科分类:医学(综合)
来源: Society of Nuclear Medicine
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【 摘 要 】

18F-FDG PET has been widely used in the management of malignant tumors. Lactate dehydrogenase A (LDHA) plays an important role in the development, invasion, and metastasis of malignancies. However, the relationship between 18F-FDG accumulation and LDHA expression has not been investigated. Methods: Retrospective analysis was conducted for 51 patients with lung adenocarcinomas who underwent 18F-FDG PET. The relationship between maximum standardized uptake value and the expression of LDHA, glucose transporter 1 (GLUT1), and hexokinase 2 (HK2) were examined. RNA interference was used to analyze the role of LDHA in tumor metabolism and growth in A549 cells. The AKT, also known as protein kinase B, pathway was also investigated to evaluate the molecular mechanisms of the relationship between LDHA expression and 18F-FDG uptake. Results: Maximum standardized uptake value was significantly higher in the LDHA high-expression group than the LDHA low-expression group (P = 0.018). GLUT1 expression in lung adenocarcinomas was positively correlated with 18F-FDG accumulation and LDHA expression whereas HK2 expression was not. Knockdown of LDHA led to a significant decrease in GLUT1 expression, 18F-FDG uptake, and cell proliferation. The activated form of AKT was also decreased after LDHA knockdown. Conclusion: LDHA increases 18F-FDG accumulation into non–small cell lung cancer, possibly by upregulation of GLUT1 expression but not HK2 expression. LDHA may modulate 18F-FDG uptake in lung adenocarcinomas via the AKT–GLUT1 pathway. These results indicate that 18F-FDG PET/CT may predict LDHA expression levels and response to anti-LDHA therapy in lung adenocarcinomas.

【 授权许可】

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