Department of Breast-Thyroid-Surgery and Cancer Center, Xiang'an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Fujian Key Laboratory of Precision Diagnosis and Treatment in Breast Cancer (Xiang'an Hospital of Xiamen University), Xiamen, China.
Cancer Res. 2023 Oct 13;83(20):3428-3441. doi: 10.1158/0008-5472.CAN-22-3432.
Sentinel lymph node (SLN) biopsy plays a critical role in axillary staging of breast cancer. However, traditional SLN mapping does not accurately discern the presence or absence of metastatic disease. Detection of SLN metastasis largely hinges on examination of frozen sections or paraffin-embedded tissues post-SLN biopsy. To improve detection of SLN metastasis, we developed a second near-infrared (NIR-II) in vivo fluorescence imaging system, pairing erbium-based rare-earth nanoparticles (ErNP) with bright down-conversion fluorescence at 1,556 nm. To visualize SLNs bearing breast cancer, ErNPs were modified by balixafortide (ErNPs@POL6326), a peptide antagonist of the chemokine receptor CXCR4. The ErNPs@POL6326 probes readily drained into SLNs when delivered subcutaneously, entering metastatic breast tumor cells specifically via CXCR4-mediated endocytosis. NIR fluorescence signals increased significantly in tumor-positive versus tumor-negative SLNs, enabling accurate determination of SLN breast cancer metastasis. In a syngeneic mouse mammary tumor model and a human breast cancer xenograft model, sensitivity for SLN metastasis detection was 92.86% and 93.33%, respectively, and specificity was 96.15% and 96.08%, respectively. Of note, the probes accurately detected both macrometastases and micrometastases in SLNs. These results overall underscore the potential of ErNPs@POL6326 for real-time visualization of SLNs and in vivo screening for SLN metastasis.
NIR-IIb imaging of a rare-earth nanoprobe that is specifically taken up by breast cancer cells can accurately detect breast cancer macrometastases and micrometastases in sentinel lymph nodes.
前哨淋巴结 (SLN) 活检在乳腺癌腋窝分期中起着至关重要的作用。然而,传统的 SLN 绘图并不能准确辨别是否存在转移性疾病。SLN 转移的检测主要取决于 SLN 活检后对冷冻切片或石蜡包埋组织的检查。为了提高 SLN 转移的检测率,我们开发了第二个近红外(NIR-II)体内荧光成像系统,将基于铒的稀土纳米粒子(ErNP)与在 1556nm 处的明亮下转换荧光相结合。为了可视化携带乳腺癌的 SLN,ErNP 通过 balixafortide(ErNPs@POL6326)进行修饰,balixafortide 是趋化因子受体 CXCR4 的肽拮抗剂。当经皮给药时,ErNPs@POL6326 探针很容易流入 SLN,通过 CXCR4 介导的内吞作用特异性进入转移性乳腺癌肿瘤细胞。在肿瘤阳性与肿瘤阴性 SLN 中,NIR 荧光信号显著增加,从而能够准确确定 SLN 乳腺癌转移。在同种小鼠乳腺肿瘤模型和人乳腺癌异种移植模型中,SLN 转移检测的灵敏度分别为 92.86%和 93.33%,特异性分别为 96.15%和 96.08%。值得注意的是,该探针可准确检测 SLN 中的大转移灶和微转移灶。这些结果总体上强调了 ErNPs@POL6326 用于实时可视化 SLN 和体内筛查 SLN 转移的潜力。
专门被乳腺癌细胞摄取的稀土纳米探针的 NIR-IIb 成像可以准确检测 SLN 中的乳腺癌大转移灶和微转移灶。