Molecular Cardiology Research Institute, Tufts Medical Center, Boston, MA, U.S.A.
Genetics, Molecular, and Cellular Biology Program, Tufts Graduate School of Biomedical Sciences, Boston, MA, U.S.A.
Clin Sci (Lond). 2024 Sep 18;138(18):1131-1150. doi: 10.1042/CS20240537.
Vascular endothelial growth factor receptor inhibitors (VEGFRis) improve cancer survival but are associated with treatment-limiting hypertension, often attributed to endothelial cell (EC) dysfunction. Using phosphoproteomic profiling of VEGFRi-treated ECs, drugs were screened for mitigators of VEGFRi-induced EC dysfunction and validated in primary aortic ECs, mice, and canine cancer patients. VEGFRi treatment significantly raised systolic blood pressure (SBP) and increased markers of endothelial and renal dysfunction in mice and canine cancer patients. α-Adrenergic-antagonists were identified as drugs that most oppose the VEGFRi proteomic signature. Doxazosin, one such α-antagonist, prevented EC dysfunction in murine, canine, and human aortic ECs. In mice with sorafenib-induced-hypertension, doxazosin mitigated EC dysfunction but not hypertension or glomerular endotheliosis, while lisinopril mitigated hypertension and glomerular endotheliosis without impacting EC function. Hence, reversing EC dysfunction was insufficient to mitigate VEGFRi-induced-hypertension in this mouse model. Canine cancer patients with VEGFRi-induced-hypertension were randomized to doxazosin or lisinopril and both agents significantly decreased SBP. The canine clinical trial supports safety and efficacy of doxazosin and lisinopril as antihypertensives for VEGFRi-induced-hypertension and the potential of trials in canines with spontaneous cancer to accelerate translation. The overall findings demonstrate the utility of phosphoproteomics to identify EC-protective agents to mitigate cardio-oncology side effects.
血管内皮生长因子受体抑制剂 (VEGFRi) 可提高癌症患者的生存率,但与治疗相关的高血压相关,这通常归因于内皮细胞 (EC) 功能障碍。使用 VEGFRi 处理的 EC 的磷酸化蛋白质组学分析,筛选出可减轻 VEGFRi 诱导的 EC 功能障碍的药物,并在原代主动脉 EC、小鼠和犬癌症患者中进行验证。VEGFRi 治疗显著升高收缩压 (SBP),并增加了小鼠和犬癌症患者内皮和肾功能障碍的标志物。α-肾上腺素能拮抗剂被鉴定为最能对抗 VEGFRi 蛋白质组学特征的药物。多沙唑嗪是一种 α-拮抗剂,可防止小鼠、犬和人主动脉 EC 中的 EC 功能障碍。在索拉非尼诱导高血压的小鼠中,多沙唑嗪减轻了 EC 功能障碍,但不能减轻高血压或肾小球内皮细胞增多症,而赖诺普利减轻了高血压和肾小球内皮细胞增多症,但不影响 EC 功能。因此,在这种小鼠模型中,逆转 EC 功能障碍不足以减轻 VEGFRi 诱导的高血压。患有 VEGFRi 诱导性高血压的犬癌症患者被随机分为多沙唑嗪或赖诺普利组,这两种药物均显著降低 SBP。犬科临床试验支持多沙唑嗪和赖诺普利作为 VEGFRi 诱导性高血压降压药的安全性和有效性,并有可能在患有自发性癌症的犬科动物中进行试验,以加速转化。总的来说,这些发现证明了磷酸化蛋白质组学在鉴定保护内皮细胞的药物以减轻心血管肿瘤学副作用方面的实用性。