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使用亲和体探针对前哨淋巴结中的转移性癌细胞进行成像及其治疗诊断方法的可能性。

Imaging of Metastatic Cancer Cells in Sentinel Lymph Nodes using Affibody Probes and Possibility of a Theranostic Approach.

机构信息

Emeritus Professor, The Nippon Dental University, Tokyo, Japan, formerly of the Department of Oral and Maxillofacial Radiology, The Nippon Dental University School of Life Dentistry at Niigata, 1-8 Hamaura-cho, Chuo-ku, Niigata 951-8580, Japan.

Department of Life Science Dentistry, The Nippon Dental University, 1-9-20 Fujimi, Chiyoda-ku, Tokyo 102-8159, Japan.

出版信息

Int J Mol Sci. 2019 Jan 19;20(2):427. doi: 10.3390/ijms20020427.

Abstract

The accurate detection of lymph node metastases is essential for treatment success in early-stage malignant cancer. Sentinel lymph node (SLN) biopsy is the most effective procedure for detecting small or micrometastases that are undetectable by conventional imaging modalities. To demonstrate a new approach for developing a more efficient SLN biopsy procedure, we reported a two-stage imaging method combining lymphoscintigraphy and near-infrared (NIR) fluorescence imaging to depict metastatic cancer cells in SLNs in vivo. Furthermore, the theranostic potential of the combined procedure was examined by cell culture and xenograft mouse model. Anti-HER2 and anti-epidermal growth factor receptor (EGFR) affibody probes were used for NIR fluorescence imaging. Strong NIR fluorescence signal intensity of the anti-EGFR affibody probe was observed in SAS cells (EGFR positive). Radioactivity in the SLNs was clearly observed in the in vivo studies. High anti-EGFR affibody NIR fluorescence intensity was observed in the metastatic lymph nodes in mice. The addition of the IR700-conjugated anti-EGFR affibody to the culture medium decreased the proliferation of SAS cells. Decreased proliferation was shown in Ki-67 immunohistochemistry in xenograft tumors. Our data suggest that a two-stage combined imaging method using lymphoscintigraphy and affibody probes may offer the direct visualization of metastatic lymph nodes as an easily applied technique in SLN biopsy. Although further animal studies are required to assess the effect of treating lymphatic metastasis in this approach, our study results provide a foundation for the further development of this promising imaging and treatment strategy for earlier lymph node metastasis detection and treatment.

摘要

准确检测淋巴结转移对于早期恶性癌症的治疗成功至关重要。前哨淋巴结 (SLN) 活检是检测常规成像方式无法检测到的小或微转移的最有效方法。为了展示一种开发更有效的 SLN 活检程序的新方法,我们报告了一种结合淋巴闪烁显像和近红外 (NIR) 荧光成像的两阶段成像方法,以在体内描绘 SLN 中的转移性癌细胞。此外,通过细胞培养和异种移植小鼠模型检查了联合程序的治疗潜力。使用抗 HER2 和抗表皮生长因子受体 (EGFR) 亲和体探针进行 NIR 荧光成像。在 SAS 细胞(EGFR 阳性)中观察到抗 EGFR 亲和体探针的强烈 NIR 荧光信号强度。在体内研究中清楚地观察到 SLN 中的放射性。在携带转移性淋巴结的小鼠中观察到高抗 EGFR 亲和体 NIR 荧光强度。将与 IR700 缀合的抗 EGFR 亲和体添加到培养基中可降低 SAS 细胞的增殖。在异种移植肿瘤的 Ki-67 免疫组化中显示出增殖减少。我们的数据表明,使用淋巴闪烁显像和亲和体探针的两阶段联合成像方法可能提供作为 SLN 活检中易于应用的技术的转移性淋巴结的直接可视化。尽管需要进一步的动物研究来评估该方法治疗淋巴转移的效果,但我们的研究结果为进一步开发这种有前途的成像和治疗策略以早期检测和治疗淋巴结转移提供了基础。

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