肿瘤来源的外泌体通过调节人卵巢癌异种移植模型中的微血管血液动力学促进肿瘤生长。
Tumor-Derived Exosomes Promote Tumor Growth Through Modulating Microvascular Hemodynamics in a Human Ovarian Cancer Xenograft Model.
机构信息
Institute of Microcirculation, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
International Center of Microvascular Medicine, Chinese Academy of Medical Sciences, Beijing, China.
出版信息
Microcirculation. 2024 Oct;31(7):e12876. doi: 10.1111/micc.12876. Epub 2024 Jul 15.
OBJECTIVE
Abnormal tumor vascular network contributes to aberrant blood perfusion and reduced oxygenation in tumors, which lead to poor efficacy of chemotherapy and radiotherapy. We aimed to explore the effects of the tumor-derived exosomes (TDEs) and C188-9 (a small molecule inhibitor of signal transducer and activator of transcription 3, STAT3) on tumor microvascular hemodynamics and determine which blood flow oscillations for various frequency intervals are responsible for these changes.
METHODS
Microvascular hemodynamics parameters were recorded using a PeriFlux 6000 EPOS system in tumor surface in a nude mouse subcutaneous xenograft model. Oscillations of laser Doppler flowmetry (LDF) signal were investigated by wavelet transform analysis.
RESULTS
TDEs facilitated tumor growth at least partially was associated with increasing blood flow in smaller vessels with lower speed and decreasing the blood flow at larger vessels with higher speed. Lower oxyhemoglobin saturation (SO) on tumor surface was aggravated by TDEs, and C188-9 treatment significantly alleviated this decrease. Wavelet transform spectral analysis revealed that TDEs increased the amplitude of oscillations in four frequency intervals related to endothelial (NO-dependent and -independent), myogenic and neurogenic activities, and C188-9 had no effect on this increase.
CONCLUSIONS
TDEs facilitated tumor growth partially was associated with increasing blood flow in distributing vessels, reducing blood perfusion in larger vessels, and lowering SO on tumor surface. Enhanced vascular smooth muscle, endothelial and neurogenic activities occurred in tumor superficial zone.
目的
异常肿瘤血管网络导致肿瘤内血液灌注和氧合异常,从而降低化疗和放疗的疗效。本研究旨在探讨肿瘤来源的外泌体(TDEs)和 C188-9(信号转导和转录激活因子 3,STAT3 的小分子抑制剂)对肿瘤微血管血液动力学的影响,并确定哪些血流振荡的不同频率间隔负责这些变化。
方法
使用 PeriFlux 6000 EPOS 系统在裸鼠皮下异种移植模型的肿瘤表面记录微血管血液动力学参数。通过小波变换分析研究激光多普勒血流仪(LDF)信号的振荡。
结果
TDEs 至少部分促进肿瘤生长与较小血管的血流增加有关,这些血管的速度较低,而较大血管的血流速度较高。TDEs 加重了肿瘤表面低氧合血红蛋白饱和度(SO),C188-9 治疗显著减轻了这种降低。小波变换谱分析显示,TDEs 增加了与内皮(NO 依赖和非依赖)、肌源性和神经源性活动相关的四个频率间隔的振荡幅度,而 C188-9 对这种增加没有影响。
结论
TDEs 促进肿瘤生长的部分原因是分布血管的血流增加,较大血管的血流灌注减少,肿瘤表面的 SO 降低。肿瘤浅层区血管平滑肌、内皮和神经源性活动增强。