University Campus II, University of Guilan, Rasht, Iran.
Department of Nuclear Pharmacy, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Biomed Pharmacother. 2024 Sep;178:117189. doi: 10.1016/j.biopha.2024.117189. Epub 2024 Jul 25.
The prevalence of breast cancer underscores the imperative for early diagnosis in guiding treatment decisions. This study introduces a novel contrast agent, Gd-DTPA-VGB3, derived from the peptide VGB3 targeting vascular endothelial growth factor receptor-1 (VEGFR1) and VEGFR2, to enhance the contrast of conventional drug Magnevist in breast tumor MRI. The MRI contrast agent was synthesized on rink amide resin via Fmoc strategy, incorporating amino acids, and coupling to diethylenetriaminepentaacetic acid (DTPA). Gadolinium (Gd)-DTPA-VGB3 displayed specific binding to VEGFR1/2 in a displacement binding assay. Gd-DTPA-VGB3 exhibited minimal cytotoxicity to normal MCF-10 cells while inhibiting 4T1 mammary carcinoma cell proliferation. Compared to Magnevist, Gd-DTPA-VGB3 demonstrated a 2.8-fold increase in contrast-to-noise ratio (CNR) (355 vs. 125). Gd-DTPA-VGB3 exhibited enhanced accumulation in 4T1 tumor-bearing mice, resulting in significant signal intensity improvement. The findings highlight Gd-DTPA-VGB3's specific binding to VEGFRs, substantiating its potential as a candidate for enhancing MRI contrast in breast cancer diagnostics.
乳腺癌的高发率强调了早期诊断在指导治疗决策方面的必要性。本研究引入了一种新型对比剂 Gd-DTPA-VGB3,它来源于靶向血管内皮生长因子受体-1(VEGFR1)和 VEGFR2 的肽 VGB3,旨在增强常规药物 Magnevist 在乳腺癌 MRI 中的对比效果。该 MRI 对比剂是通过 Fmoc 策略在 rink 酰胺树脂上合成的,其中包含氨基酸,并与二乙三胺五乙酸(DTPA)偶联。在置换结合测定中,Gd-DTPA-VGB3 显示出对 VEGFR1/2 的特异性结合。Gd-DTPA-VGB3 对正常 MCF-10 细胞表现出最小的细胞毒性,同时抑制 4T1 乳腺癌细胞的增殖。与 Magnevist 相比,Gd-DTPA-VGB3 的对比噪声比(CNR)增加了 2.8 倍(355 比 125)。Gd-DTPA-VGB3 在携带 4T1 肿瘤的小鼠中表现出增强的积累,导致信号强度的显著改善。这些发现强调了 Gd-DTPA-VGB3 对 VEGFRs 的特异性结合,证实了其作为增强乳腺癌诊断中 MRI 对比的候选物的潜力。