Center for Molecular and Biomolecular Imaging, Department of Chemistry, Duke University, Durham, NC 27708, USA.
Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3693-7. doi: 10.1073/pnas.1000386107. Epub 2010 Feb 8.
Early and specific detection of metastatic cancer cells in the lung (the most common organ targeted by metastases) could significantly improve cancer treatment outcomes. However, the most widespread lung imaging methods use ionizing radiation and have low sensitivity and/or low specificity for cancer cells. Here we address this problem with an imaging method to detect submillimeter-sized metastases with molecular specificity. Cancer cells are targeted by iron oxide nanoparticles functionalized with cancer-binding ligands, then imaged by high-resolution hyperpolarized (3)He MRI. We demonstrate in vivo detection of pulmonary micrometastates in mice injected with breast adenocarcinoma cells. The method not only holds promise for cancer imaging but more generally suggests a fundamentally unique approach to molecular imaging in the lungs.
早期和特异性检测肺部(转移最常见的器官)中的转移性癌细胞,可以显著改善癌症治疗效果。然而,最广泛使用的肺部成像方法使用电离辐射,对癌细胞的灵敏度和/或特异性较低。在这里,我们使用一种具有分子特异性的成像方法来解决这个问题,可以检测亚毫米大小的转移灶。用与癌细胞结合的配体功能化的氧化铁纳米颗粒来靶向癌细胞,然后通过高分辨率的超极化(3)He MRI 进行成像。我们在注射乳腺癌细胞的小鼠中证明了肺部微转移灶的体内检测。该方法不仅有望用于癌症成像,而且更普遍地为肺部的分子成像提供了一种独特的方法。
Proc Natl Acad Sci U S A. 2010-2-8
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