Optical Imaging Laboratory, Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
Department of Electrical and Computer Engineering, Texas A&M University, College Station, TX 77843, USA.
Sci Rep. 2016 Dec 21;6:39616. doi: 10.1038/srep39616.
Metastasis causes as many as 90% of cancer-related deaths, especially for the deadliest skin cancer, melanoma. Since hematogenous dissemination of circulating tumor cells is the major route of metastasis, detection and destruction of circulating tumor cells are vital for impeding metastasis and improving patient prognosis. Exploiting the exquisite intrinsic optical absorption contrast of circulating melanoma cells, we developed dual-wavelength photoacoustic flow cytography coupled with a nanosecond-pulsed melanoma-specific laser therapy mechanism. We have successfully achieved in vivo label-free imaging of rare single circulating melanoma cells in both arteries and veins of mice. Further, the photoacoustic signal from a circulating melanoma cell immediately hardware-triggers a lethal pinpoint laser irradiation to kill it on the spot in a thermally confined manner without causing collateral damage. A pseudo-therapy study including both in vivo and in vitro experiments demonstrated the performance and the potential clinical value of our method, which can facilitate early treatment of metastasis by clearing circulating tumor cells from vasculature.
转移导致多达 90%的癌症相关死亡,尤其是对于最致命的皮肤癌——黑色素瘤。由于循环肿瘤细胞的血源性播散是转移的主要途径,因此检测和破坏循环肿瘤细胞对于阻止转移和改善患者预后至关重要。我们利用循环黑色素瘤细胞出色的固有光学吸收对比度,开发了双波长光声流动细胞术,并结合纳秒脉冲黑色素瘤特异性激光治疗机制。我们已经成功地在小鼠的动脉和静脉中实现了对罕见的单个循环黑色素瘤细胞的无标记体内成像。此外,来自循环黑色素瘤细胞的光声信号立即通过硬件触发致死性的精确激光照射,以热限制的方式当场杀死它,而不会造成附带损伤。包括体内和体外实验在内的假治疗研究证明了我们方法的性能和潜在的临床价值,它可以通过从脉管系统清除循环肿瘤细胞来促进转移的早期治疗。