Lasič Samo, Oredsson Stina, Partridge Savannah C, Saal Lao H, Topgaard Daniel, Nilsson Markus, Bryskhe Karin
CR Development AB, Lund, Sweden.
Department of Biology, Lund University, Lund, Sweden.
NMR Biomed. 2016 May;29(5):631-9. doi: 10.1002/nbm.3504. Epub 2016 Feb 29.
Although diffusion MRI has shown promise for the characterization of breast cancer, it has low specificity to malignant subtypes. Higher specificity might be achieved if the effects of cell morphology and molecular exchange across cell membranes could be disentangled. The quantification of exchange might thus allow the differentiation of different types of breast cancer cells. Based on differences in diffusion rates between the intra- and extracellular compartments, filter exchange spectroscopy/imaging (FEXSY/FEXI) provides non-invasive quantification of the apparent exchange rate (AXR) of water between the two compartments. To test the feasibility of FEXSY for the differentiation of different breast cancer cells, we performed experiments on several breast epithelial cell lines in vitro. Furthermore, we performed the first in vivo FEXI measurement of water exchange in human breast. In cell suspensions, pulsed gradient spin-echo experiments with large b values and variable pulse duration allow the characterization of the intracellular compartment, whereas FEXSY provides a quantification of AXR. These experiments are very sensitive to the physiological state of cells and can be used to establish reliable protocols for the culture and harvesting of cells. Our results suggest that different breast cancer subtypes can be distinguished on the basis of their AXR values in cell suspensions. Time-resolved measurements allow the monitoring of the physiological state of cells in suspensions over the time-scale of hours, and reveal an abrupt disintegration of the intracellular compartment. In vivo, exchange can be detected in a tumor, whereas, in normal tissue, the exchange rate is outside the range experimentally accessible for FEXI. At present, low signal-to-noise ratio and limited scan time allows the quantification of AXR only in a region of interest of relatively large tumors.
尽管扩散磁共振成像在乳腺癌特征表征方面已显示出前景,但它对恶性亚型的特异性较低。如果能够区分细胞形态和跨细胞膜分子交换的影响,可能会实现更高的特异性。因此,交换的量化可能有助于区分不同类型的乳腺癌细胞。基于细胞内和细胞外间隙之间扩散速率的差异,过滤交换光谱法/成像(FEXSY/FEXI)可对两间隙之间水的表观交换率(AXR)进行无创量化。为了测试FEXSY区分不同乳腺癌细胞的可行性,我们在几种乳腺上皮细胞系上进行了体外实验。此外,我们首次对人体乳腺中的水交换进行了体内FEXI测量。在细胞悬液中,采用大b值和可变脉冲持续时间的脉冲梯度自旋回波实验可表征细胞内间隙,而FEXSY可对AXR进行量化。这些实验对细胞的生理状态非常敏感,可用于建立可靠的细胞培养和收获方案。我们的结果表明,不同的乳腺癌亚型可根据其在细胞悬液中的AXR值进行区分。时间分辨测量可在数小时的时间尺度上监测悬液中细胞的生理状态,并揭示细胞内间隙的突然解体。在体内,肿瘤中可检测到交换,而在正常组织中,交换率超出了FEXI实验可及的范围。目前,低信噪比和有限的扫描时间仅允许在相对较大肿瘤感兴趣区域内对AXR进行量化。