Ma Mengjie, Liang Jianye, Zhang Dong, Xu Xi, Cheng Qingqing, Xiao Zeyu, Shi Changzheng, Luo Liangping
Medical Imaging Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Department of Medical Imaging, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
Front Oncol. 2021 Apr 30;11:672047. doi: 10.3389/fonc.2021.672047. eCollection 2021.
This study aimed to investigate the effectiveness of intravoxel incoherent motion (IVIM) diffusion-weighted imaging (DWI) and blood oxygen level-dependent (BOLD) magnetic resonance imaging (MRI) in monitoring tumor responses to antiangiogenic therapy combined with hypoxia-activated prodrugs (HAPs).
Establishing colon cancer xenograft model by subcutaneously injecting the HCT116 cell line into BALB/C nude mice. Twenty-four tumor-bearing mice were randomly divided into four groups and injected with bevacizumab combined with TH-302 (A), bevacizumab (B), TH-302 (C), or saline (D) on days 1, 4, 7, 10 and 13. Functional MRI was performed before and at 3, 6, 9, 12 and 15 days after treatment. Pathologic examinations, including HE staining, HIF-1α and CD31 immunohistochemical staining, and TUNEL and Ki-67 immunofluorescent staining, were performed after the last scan.
At the end of the study, Group A showed the lowest tumor volume, followed by Groups B, C, and D (F=120.652, P<0.001). For pathologic examinations, Group A showed the lowest percentage of CD31 staining (F=73.211, P<0.001) and Ki-67 staining (F=231.170, P<0.001), as well as the highest percentage of TUNEL staining (F=74.012, P<0.001). Moreover, the D* and f values exhibited positive correlations with CD31 (r=0.868, P<0.001, and r=0.698, P=0.012, respectively). R2* values was positively correlated with HIF-1α (r=0.776, P=0.003). D values were positively correlated with TUNEL (r=0.737, P=0.006) and negatively correlated with Ki-67 (r=0.912, P<0.001). The standard ADC values were positive correlated with TUNEL (r=0.672, P=0.017) and negative correlated with Ki-67 (r=0.873, P<0.001).
Anti-angiogenic agents combined with HAP can inhibit tumor growth effectively. In addition, IVIM-DWI and BOLD-MRI can be used to monitor the tumor microenvironment, including perfusion, hypoxia, cell apoptosis and proliferation, in a noninvasive manner.
本研究旨在探讨体素内不相干运动(IVIM)扩散加权成像(DWI)和血氧水平依赖(BOLD)磁共振成像(MRI)在监测肿瘤对抗血管生成治疗联合乏氧激活前体药物(HAPs)反应中的有效性。
通过将HCT116细胞系皮下注射到BALB/C裸鼠体内建立结肠癌异种移植模型。24只荷瘤小鼠随机分为四组,分别在第1、4、7、10和13天注射贝伐单抗联合TH-302(A组)、贝伐单抗(B组)、TH-302(C组)或生理盐水(D组)。在治疗前及治疗后3、6、9、12和15天进行功能MRI检查。在最后一次扫描后进行病理检查,包括HE染色、HIF-1α和CD31免疫组化染色以及TUNEL和Ki-67免疫荧光染色。
研究结束时,A组肿瘤体积最小,其次是B组、C组和D组(F = 120.652,P < 0.001)。病理检查显示,A组CD31染色百分比(F = 73.211,P < 0.001)和Ki-67染色百分比(F = 231.170,P < 0.001)最低,TUNEL染色百分比最高(F = 74.012,P < 0.001)。此外,D值和f值与CD31呈正相关(分别为r = 0.868,P < 0.001和r = 0.698,P = 0.012)。R2值与HIF-1α呈正相关(r = 0.776,P = 0.003)。D值与TUNEL呈正相关(r = 0.737,P = 0.006),与Ki-67呈负相关(r = 0.912,P < 0.001)。标准ADC值与TUNEL呈正相关(r = 0.672,P = 0.017),与Ki-67呈负相关(r = 0.873,P < 0.001)。
抗血管生成药物联合HAP可有效抑制肿瘤生长。此外,IVIM-DWI和BOLD-MRI可用于以非侵入性方式监测肿瘤微环境,包括灌注、缺氧、细胞凋亡和增殖。