Department of Biomedical Engineering, University of Southern California, Los Angeles, California 90089, USA.
Biotechnol Bioeng. 2013 Oct;110(10):2697-705. doi: 10.1002/bit.24923. Epub 2013 Apr 22.
In this article, we investigate the application of contactless high frequency ultrasound microbeam stimulation (HFUMS) for determining the invasion potential of breast cancer cells. In breast cancer patients, the finding of tumor metastasis significantly worsens the clinical prognosis. Thus, early determination of the potential of a tumor for invasion and metastasis would significantly impact decisions about aggressiveness of cancer treatment. Recent work suggests that invasive breast cancer cells (MDA-MB-231), but not weakly invasive breast cancer cells (MCF-7, SKBR3, and BT-474), display a number of neuronal characteristics, including expression of voltage-gated sodium channels. Since sodium channels are often co-expressed with calcium channels, this prompted us to test whether single-cell stimulation by a highly focused ultrasound microbeam would trigger Ca(2+) elevation, especially in highly invasive breast cancer cells. To calibrate the diameter of the microbeam ultrasound produced by a 200-MHz single element LiNbO3 transducer, we focused the beam on a wire target and performed a pulse-echo test. The width of the beam was ∼17 µm, appropriate for single cell stimulation. Membrane-permeant fluorescent Ca(2+) indicators were utilized to monitor Ca(2+) changes in the cells due to HFUMS. The cell response index (CRI), which is a composite parameter reflecting both Ca(2+) elevation and the fraction of responding cells elicited by HFUMS, was much greater in highly invasive breast cancer cells than in the weakly invasive breast cancer cells. The CRI of MDA-MB-231 cells depended on peak-to-peak amplitude of the voltage driving the transducer. These results suggest that HFUMS may serve as a novel tool to determine the invasion potential of breast cancer cells, and with further refinement may offer a rapid test for invasiveness of tumor biopsies in situ.
在本文中,我们研究了接触式高频超声微束刺激(HFUMS)在确定乳腺癌细胞侵袭潜力中的应用。在乳腺癌患者中,肿瘤转移的发现显著恶化了临床预后。因此,早期确定肿瘤侵袭和转移的潜力将对癌症治疗的侵袭性决策产生重大影响。最近的工作表明,侵袭性乳腺癌细胞(MDA-MB-231),但不是弱侵袭性乳腺癌细胞(MCF-7、SKBR3 和 BT-474),表现出许多神经元特征,包括电压门控钠离子通道的表达。由于钠离子通道通常与钙通道共同表达,这促使我们测试单个细胞是否通过高度聚焦的超声微束刺激会引发 Ca(2+)升高,特别是在高度侵袭性的乳腺癌细胞中。为了校准 200-MHz 单元素 LiNbO3 换能器产生的微束超声的直径,我们将光束聚焦在金属丝靶标上并进行了脉冲回波测试。光束的宽度约为 17μm,适用于单细胞刺激。利用膜透性荧光 Ca(2+)指示剂监测由于 HFUMS 引起的细胞内 Ca(2+)变化。细胞反应指数(CRI)是一个综合参数,反映了 HFUMS 引起的 Ca(2+)升高和反应细胞的分数,在高度侵袭性的乳腺癌细胞中比在弱侵袭性的乳腺癌细胞中要大得多。MDA-MB-231 细胞的 CRI 取决于驱动换能器的电压的峰峰值幅度。这些结果表明,HFUMS 可以作为一种确定乳腺癌细胞侵袭潜力的新工具,并且随着进一步的改进,它可能为原位肿瘤活检的侵袭性提供快速测试。