Yu Jing, Du Xia, Zhang Shuai, Long Jinhua, Wu Peng, Li Zongxue, Lyu Xinyue, Hong Qin, Chen Pengyu, Gao Bo
Department of Radiology, The Affiliated Hospital of Guizhou Medical University, Guiyang 550004, Guizhou Province, China.
Department of Head & Neck, The Affiliated Tumor Hospital of Guizhou Medical University, Guiyang 550004, Guizhou Province, China.
Mol Ther Oncol. 2024 Aug 8;32(3):200858. doi: 10.1016/j.omton.2024.200858. eCollection 2024 Sep 19.
Tumor vascular normalization (TVN) is associated with antitumor therapeutic efficacy in nasopharyngeal carcinoma (NPC). However, the short time window of TVN is the biggest hindrance to its wide clinical application. We investigated whether targeting transforming growth factor beta can enhance the TVN effect of bevacizumab (BEV)-induced patient-derived xenograft (PDX) models of NPC. We constructed mouse subcutaneous PDX models of NPC and classified the mice into four drug-treatment groups, namely placebo control, galunisertib, BEV, and galunisertib + BEV. We performed MRI multi-parameter examinations at different time points and evaluated the vascular density, vascular structure, and tumor hypoxia microenvironment by histopathology. The efficacy of chemotherapy and drug delivery was evaluated by administering cisplatin. We found that combined therapy with galunisertib and BEV significantly delayed tumor growth, enhanced the TVN effect, and improved chemotherapeutic efficacy compared with monotherapy. Mechanistically, galunisertib reversed the epithelial-mesenchymal transition process and inhibited the expression of hypoxia-inducible factor 1α and vascular endothelial growth factor by downregulating LAMC2. Correlation analysis of MRI data and pathological indicators showed that there was a good correlation between them.
肿瘤血管正常化(TVN)与鼻咽癌(NPC)的抗肿瘤治疗效果相关。然而,TVN的时间窗较短是其广泛临床应用的最大障碍。我们研究了靶向转化生长因子β是否能增强贝伐单抗(BEV)诱导的NPC患者来源异种移植(PDX)模型的TVN效应。我们构建了NPC小鼠皮下PDX模型,并将小鼠分为四个药物治疗组,即安慰剂对照组、加芦尼替尼组、BEV组和加芦尼替尼+BEV组。我们在不同时间点进行了MRI多参数检查,并通过组织病理学评估了血管密度、血管结构和肿瘤缺氧微环境。通过给予顺铂评估化疗和药物递送的疗效。我们发现,与单一疗法相比,加芦尼替尼和BEV联合治疗显著延迟了肿瘤生长,增强了TVN效应,并提高了化疗疗效。机制上,加芦尼替尼通过下调LAMC2逆转上皮-间质转化过程,并抑制缺氧诱导因子1α和血管内皮生长因子的表达。MRI数据与病理指标的相关性分析表明,两者之间存在良好的相关性。