Department of Ultrasound, Zhongda Hospital, Medical School, Southeast University, 87 Dingjiaqiao Road, Nanjing, 210009, People's Republic of China.
Department of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, 3155 Porter Drive, Palo Alto, CA, 94305, USA.
Mol Imaging Biol. 2022 Apr;24(2):333-340. doi: 10.1007/s11307-021-01680-3. Epub 2021 Nov 17.
PURPOSE: Accurate identification and assessment of sentinel lymph node (SLN) using noninvasive imaging methods can play a vital role in tumor staging, surgical planning, and prognostic evaluation. In this study, we assessed the efficacy of B7-H3-targeted molecular-ultrasound imaging for the early SLN detection, and characterization in a mouse model of orthotopic breast cancer. PROCEDURES: We established a mouse breast cancer model with lymph node metastasis by injecting MAD-MB 231 cells which were engineered to express firefly luciferase reporter gene into the fat pad of the right 4th mammary gland in female BALB/c nude mice. The sole lymph node (LN) close to the tumor was regarded as the SLN for imaging investigation, which included metastatic and non-metastatic SLNs. The LN in the right 4th mammary gland from normal mice was used as normal control (normal mice LN). The commercially available preclinical streptavidin-coated, perfluorocarbon-containing lipid-shelled microbubbles (VisualSonics, Toronto, Canada) were used to generate B7-H3-targeted microbubbles (MB) and control microbubbles (MB). Then, ultrasound molecular imaging (USMI) was performed using a high-resolution transducer (MS250; center frequency, 21 MHz; Vevo 2100; VisualSonics, Toronto, Canada) after intravenous injection of microbubbles. RESULTS: The SLN was clearly detected and located under conventional (B-mode) and contrast-enhanced ultrasonography with microbubble injection. The metastatic SLNs showed a markedly higher signal from B7-H3-targeted microbubbles (MB) compared to the non-metastatic SLNs and normal LNs. The metastatic SLN was further confirmed by ex vivo bioluminescence imaging and eventually verified by histological analysis. CONCLUSIONS: Our findings suggest the potential value of USMI using B7-H3 targeted microbubbles in breast cancer and establish an effective imaging method for the non-invasive detection and characterization of SLN.
目的:使用非侵入性成像方法准确识别和评估前哨淋巴结 (SLN) 在肿瘤分期、手术规划和预后评估中起着至关重要的作用。在本研究中,我们评估了 B7-H3 靶向分子超声成像在荷瘤原位乳腺癌小鼠模型中早期 SLN 检测和特征中的作用。
方法:我们通过将表达萤火虫荧光素酶报告基因的 MAD-MB 231 细胞注入雌性 BALB/c 裸鼠右第 4 乳腺脂肪垫中,建立了具有淋巴结转移的乳腺癌小鼠模型。靠近肿瘤的唯一淋巴结 (LN) 被视为 SLN 进行成像研究,其中包括转移性和非转移性 SLN。来自正常小鼠的右第 4 乳腺中的 LN 用作正常对照 (正常小鼠 LN)。使用市售的预临床链霉亲和素包被的全氟碳脂质壳微泡 (VisualSonics,多伦多,加拿大) 生成 B7-H3 靶向微泡 (MB) 和对照微泡 (MB)。然后,在静脉注射微泡后,使用高分辨率换能器 (MS250;中心频率,21 MHz;Vevo 2100;VisualSonics,多伦多,加拿大) 进行超声分子成像 (USMI)。
结果:在注射微泡后,通过常规 (B 模式) 和对比增强超声可以清楚地检测到 SLN 并定位。与非转移性 SLN 和正常 LN 相比,转移性 SLN 显示出来自 B7-H3 靶向微泡 (MB) 的信号明显更高。通过离体生物发光成像进一步证实了转移性 SLN,并最终通过组织学分析进行了验证。
结论:我们的研究结果表明,使用 B7-H3 靶向微泡的 USMI 具有潜在的价值,可用于乳腺癌,并建立了一种用于非侵入性检测和特征描述 SLN 的有效成像方法。
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