应用[18F]FLT/PET技术评估小鼠4T1乳腺肿瘤模型中迷迭香酸的肿瘤演变及抗肿瘤活性监测

Jousie Michel Pereira, Brígida Gomes de Almeida Schirmer, Marina Rios Araujo, Leonardo T. C. Nascimento, Andrea Vidal Ferreira, Aline de Biasi Bassani Gonçalves, Lucíola da Silva Barcelos, Geovanni Dantas Cassali, Marina Bicalho Silveira, Juliana Batista da Silva, Carlos Malamut
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摘要

在正电子发射断层扫描(PET)中使用示踪剂18F-fluoro-3'-deoxy-3'-L-fluorothymidine ([18F]FLT)已被证明是评估肿瘤侵袭性和早期治疗反应的有效工具。在本研究中,我们研究了[18F]FLT/PET在研究迷迭香酸(RA)在高浸润性乳腺癌中的抗肿瘤和抗肺转移作用的适用性。将4T1乳腺癌细胞注射到Balb/c雌性小鼠的侧腹。在接种肿瘤细胞后的第21天,每天给予RA治疗。[18F]采用FLT/PET显像评价原发肿瘤和肺转移灶对RA治疗的反应。PET图像显示RA治疗后小鼠肺部FLT摄取减少[18F]。RA的抗肿瘤作用似乎与抑制原发肿瘤的细胞迁移、细胞增殖和血管形成有关。此外,RA可以调节炎症反应,减少原发肿瘤中肥大细胞和中性粒细胞的积累以及肺中巨噬细胞的积累。总之,[18F]FLT/PET在4T1乳腺肿瘤模型中显示了RA的抗肿瘤和抗转移作用。此外,研究结果表明,RA调节肿瘤血管生成和炎症,在4T1乳腺癌模型中产生抗肿瘤和抗转移作用。
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Use of [18F]FLT/PET for assessing the tumor evolution and monitoring the antitumor activity of rosmarinic acid in a mouse 4T1 breast tumor model
The use of the tracer 18F-fluoro-3'-deoxy-3'-L-fluorothymidine ([18F]FLT) in positron emission tomography (PET) has been shown to be an effective tool for assessing tumor aggressiveness and early response to therapy. In this study, we investigated the applicability of [18F]FLT/PET to study the antitumor and anti–lung metastatic effects of rosmarinic acid (RA) in highly invasive breast cancer. 4T1 mammary carcinoma cells were injected into the flank of female Balb/c mice. The animals were treated daily with RA until day 21 after the inoculation of tumor cells. [18F]FLT/PET imaging was used to evaluate the response of primary tumors and lung metastases to RA treatment. PET Images showed a decreased [18F]FLT uptake in the lungs of mice after RA treatment. The antitumor effect of RA appears to be related to the inhibition of cell migration, cell proliferation, and blood vessel formation in the primary tumor. Furthermore, the inflammatory response was modulated by RA, which reduced the accumulation of mast cells and neutrophils in the primary tumor and of macrophages in the lungs. In conclusion, [18F]FLT/PET demonstrates the antitumor and antimetastatic effects of RA in a 4T1 breast tumor model. Furthermore, the findings suggest that RA modulates tumor angiogenesis and inflammation, resulting in antitumor and antimetastatic effects in a 4T1 breast carcinoma model.
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