期刊论文详细信息
Journal of Nuclear Medicine
18F-FDG Uptake in Squamous Cell Carcinoma of the Cervix Is Correlated with Glucose Transporter 1 Expression
Chiung-Ru Lai1  Jenn-Tzong Chen1  Koon-Kwan Ng1  Wuu-Jyh Lin1  Lai-Chu See1  Tzu-Chen Yen1  Wen-Jie Chen1  Chou Wu Yah-Huei1  Swei Hsueh1  Chyong-Huey Lai1  Shih-Ya Ma1 
关键词: glucose transporter 1;    squamous cell carcinoma;    cervical cancer;   
DOI  :  
学科分类:医学(综合)
来源: Society of Nuclear Medicine
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【 摘 要 】

This prospective study investigates the relationship between glucose transporter-1 (Glut-1) expression and PET images using 18F-FDG and its uptake and compares them with the tumor status (primary vs. recurrent or persistent), initial grade of histologic differentiation, and International Federation of Gynecologic Obstetrics (FIGO) staging for cervical cancer patients. Methods: A dual-phase 18F-FDG PET scan was performed on 51 participants within the 2 wk before surgery or biopsy. 18F-FDG uptake was quantified by calculating standardized uptake values (SUVs). After 18F-FDG PET scanning, 51 histologically proven squamous cell carcinoma specimens were examined to determine their degree of differentiation, using hematoxylin and eosin staining, and the expression of Glut-1 by an immunohistochemical stain. Twenty normal cervical and 20 cervical intraepithelial neoplasia (CIN) sets of tissue were also used to compare the results of Glut-1 expression in these tissues. The expression of Glut-1 was the product of (the intensity [with grades 0–3, defined qualitatively]) with (percentages of the lesion area that were positive). The results of Glut-1 expression were analyzed in combination with the SUVs (SUV1 was that at 40 min and SUV2 was that at 3 h), tumor status, initial cell differentiation, and FIGO staging. Results: Significant overexpression of Glut-1 was noted in 48 of the 51 (94.1%) cancer specimens. None or only minimal expression of Glut-1 was observed in basal layers of normal and CIN tissues. Significant positive correlation was observed between Glut-1 expression and the SUVs in cervical cancer specimens (r = 0.74, P < 0.000 for SUV1 and r = 0.65, P < 0.000 for SUV2). In recurrent or persistent tumor, tumor size was significantly associated with both Glut-1 expression (r = 0.508, P = 0.011) and SUV1 (r = 0. 456, P = 0.025). For recurrent or persistent tumor, only SUV1 reached statistical significance when compared with lymph node metastasis (P = 0.0226). Conclusion: Glut-1 expression was related to 18F-FDG uptake in cervical cancer patients. Recurrent or persistent cervical cancer tumor had significantly higher Glut-1 expression than metastatic lymph nodes. The values of SUV and the expression of Glut-1 did not correlate with the initial grade of histologic differentiation and FIGO staging.

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