Imai Toru, Muz Barbara, Yeh Cheng-Hung, Yao Junjie, Zhang Ruiying, Azab Abdel Kareem, Wang Lihong
a Department of Biomedical Engineering , Washington University in St. Louis , St. Louis , MO , USA.
b Department of Radiation Oncology , Cancer Biology Division, Washington University in St. Louis School of Medicine , St. Louis , MO , USA.
Cancer Biol Ther. 2017 Feb;18(2):101-105. doi: 10.1080/15384047.2016.1276137. Epub 2017 Jan 3.
Using photoacoustic microscopy (PAM), we evaluated non-invasively oxygenation and vascularization in vivo due to multiple myeloma (MM) progression. Mice injected with MM.1S-GFP were monitored with a fluorescence microscope for tumor progression. In vivo PAM of the cerebral bone marrow quantified the total oxygen saturation (sO). At 28 days after the MM cell injection, the total sO had decreased by half in the developing tumor regions, while in the non-tumor regions it had decreased by 20% compared with the value at one day post MM injection. The blood vessel density was reduced by 35% in the developing tumor regions, while in the non-tumor regions it was reduced by 8% compared with the value at one day post MM injection. Hence, PAM corroborated the development of hypoxia due to MM progression and demonstrated decreased vascularization surrounding the tumor areas.
我们使用光声显微镜(PAM)对多发性骨髓瘤(MM)进展导致的体内氧合和血管生成进行了非侵入性评估。对注射了MM.1S-GFP的小鼠用荧光显微镜监测肿瘤进展情况。对脑骨髓进行体内光声显微镜检查,以量化总氧饱和度(sO)。在注射MM细胞28天后,正在形成肿瘤的区域总sO降低了一半,而在非肿瘤区域,与注射MM后一天的值相比降低了20%。正在形成肿瘤的区域血管密度降低了35%,而在非肿瘤区域,与注射MM后一天的值相比降低了8%。因此,光声显微镜证实了MM进展导致缺氧的发生,并显示肿瘤区域周围的血管生成减少。