Jiang An-Na, Liu Jing-Tao, Zhao Kun, Wu Hao, Wang Song, Yan Kun, Yang Wei
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Pharmacy, Peking University Cancer Hospital & Institute, Beijing, China.
Front Oncol. 2020 Nov 18;10:561805. doi: 10.3389/fonc.2020.561805. eCollection 2020.
To determine whether the specific inhibitor of matrix metalloproteinase (MMP)-batimastat (BB-94)-could decrease the progression of liver tumor after radiofrequency ablation (RFA) and achieve better therapeutic efficacy in an animal model.
experiments, the proliferation of H22 liver tumor cells was detected by CCK 8 assay and cell migration was detected by Transwell method. experiments, H22 murine liver tumors were used. First, 32 mice with one tumor were randomized into four groups (n = 8 each group): control (PBS only), RFA alone (65°C, 5 min), BB-94 (30 mg/kg), RFA+BB-94. The growth rate of the residual tumor and the end point survival were calculated and the pathologic changes were evaluated. Secondly, a total of 48 tumors in 24 animals (paired tumors) were randomized into three groups (n = 8 each group): control, RFA alone, RFA+BB-94. Each mouse was implanted with two tumors subcutaneously, one tumor was treated by RFA and the other was evaluated for distant metastasis after applying BB-94.
, the proliferation assay demonstrated higher proliferation ability after heat treatment (0.82 ± 0.07 1.27 ± 0.08, P = 0.008), and it could be inhibited by BB-94 (1.27 ± 0.08 0.67 ± 0.06, P = 0.001). In the cell migration assay, the H22 cells demonstrated enhanced tumor invasiveness in the heat group than the control group (33.7 ± 2.1 19.7 ± 4.9, P = 0.011). And it could be significantly suppressed after BB-94 incubation (33.7 ± 2.1 23.0 ± 4.6, P = 0.009). With one tumor animal, the growth rate of the residual tumor in the BB-94+RFA group was slower than that in the RFA alone group (P = 0.003). And combination of BB-94 could significantly prolong the survival of the mice (40.3 ± 1.4d 47.1 ± 1.3d, P = 0.002). The expression of CD31 and VEGF at the coagulation margin were decreased after combined with BB-94. With two tumors animal, the growth of metastasis tumor in the BB-94+RFA group was slower than that in the RFA group (P < 0.001).
BB-94 combined with RFA reduced the invasiveness of the liver tumor and improved the end-point survival. Our data suggested that targeting the MMP process with the specific inhibition could help to increase overall ablation efficacy.
确定基质金属蛋白酶(MMP)特异性抑制剂batimastat(BB - 94)能否降低射频消融(RFA)后肝肿瘤的进展,并在动物模型中获得更好的治疗效果。
实验中,采用CCK 8法检测H22肝肿瘤细胞的增殖情况,采用Transwell法检测细胞迁移情况。实验使用H22小鼠肝肿瘤。首先,将32只患有单个肿瘤的小鼠随机分为四组(每组n = 8):对照组(仅注射PBS)、单纯RFA组(65°C,5分钟)、BB - 94组(30 mg/kg)、RFA + BB - 94组。计算残余肿瘤的生长速率和终点生存率,并评估病理变化。其次,将24只动物(成对肿瘤)中的48个肿瘤随机分为三组(每组n = 8):对照组、单纯RFA组、RFA + BB - 94组。每只小鼠皮下植入两个肿瘤,一个肿瘤接受RFA治疗,另一个在应用BB - 94后评估远处转移情况。
增殖实验表明,热处理后增殖能力更高(0.82±0.07对1.27±0.08,P = 0.008),且可被BB - 94抑制(1.27±0.08对0.67±0.06,P = 0.001)。在细胞迁移实验中,H22细胞在热处理组中的肿瘤侵袭性比对照组增强(33.7±2.1对19.7±4.9,P = 0.011)。BB - 94孵育后可显著抑制(33.7±2.1对23.0±4.6,P = 0.009)。对于单肿瘤动物,BB - 94 + RFA组残余肿瘤的生长速率比单纯RFA组慢(P = 0.003)。并且BB - 94联合使用可显著延长小鼠的生存期(40.3±1.4天对47.1±1.3天,P = 0.002)。联合BB - 94后,凝血边缘处CD31和VEGF的表达降低。对于双肿瘤动物,BB - 94 + RFA组转移瘤的生长比RFA组慢(P < 0.001)。
BB - 94联合RFA可降低肝肿瘤的侵袭性并提高终点生存率。我们的数据表明,用特异性抑制剂靶向MMP过程有助于提高整体消融疗效。