Gao Jin-Hang, Wang Chun-Hui, Tong Huan, Wen Shi-Lei, Huang Zhi-Yin, Tang Cheng-Wei
Division of Peptides Related with Human Diseases, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.
Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu, China.
Sci Rep. 2015 Nov 16;5:16382. doi: 10.1038/srep16382.
AZD6244 (ARRY-142886), a highly selective MAPK-ERK kinase inhibitor, has shown excellent clinical efficacy in many tumors. However, the anti-tumor and anti-angiogenesis efficacy of AZD6244 on gastric cancer has not been well characterized. In this study, high p-ERK expression was associated with advanced TNM stage, increased lymphovascular invasion and poor survival. For absence of NRAS, KRAS and BRAF mutation, SGC7901 and BGC823 gastric cancer cells were relative resistance to AZD6244 in vitro. And such resistance was not attributed to the insufficient inhibition of ERK phosphorylation. However, tumor growth was significantly suppressed in SGC7901 xenografts by blockage of angiogenesis. This result was further supported by suppression of tube formation and migration in HUVEC cells after treatment with AZD6244. Moreover, the anti-angiogenesis effect of AZD6244 may predominantly attribute to its modulation on VEGF through p-ERK - c-Fos - HIF-1α integrated signal pathways. In conclusions, High p-ERK expression was associated with advanced TNM stage, increased lymphovascular invasion and poor survival. Targeting inhibition of p-ERK by AZD6244 suppress gastric cancer xenografts by blockage of angiogenesis without systemic toxicity. The anti-angiogenesis effect afford by AZD6244 may attribute to its modulation on p-ERK - c-Fos - HIF-1α - VEGF integrated signal pathways.
AZD6244(ARRY-142886)是一种高度选择性的丝裂原活化蛋白激酶-细胞外信号调节激酶(MAPK-ERK)抑制剂,已在多种肿瘤中显示出优异的临床疗效。然而,AZD6244对胃癌的抗肿瘤和抗血管生成疗效尚未得到充分表征。在本研究中,高磷酸化细胞外信号调节激酶(p-ERK)表达与晚期TNM分期、淋巴管浸润增加及生存率低相关。由于不存在神经母细胞瘤RAS病毒癌基因同源物(NRAS)、KRAS原癌基因、GTP酶(KRAS)和B-Raf原癌基因,丝氨酸/苏氨酸激酶(BRAF)突变,人胃癌细胞系SGC7901和人胃癌细胞系BGC823在体外对AZD6244相对耐药。并且这种耐药性并非归因于ERK磷酸化抑制不足。然而,通过阻断血管生成,SGC7901异种移植瘤的肿瘤生长受到显著抑制。用AZD6244处理后,人脐静脉内皮细胞(HUVEC)中管腔形成和迁移的抑制进一步支持了这一结果。此外,AZD6244的抗血管生成作用可能主要归因于其通过p-ERK - c-Fos - 缺氧诱导因子-1α(HIF-1α)整合信号通路对血管内皮生长因子(VEGF)的调节。总之,高p-ERK表达与晚期TNM分期、淋巴管浸润增加及生存率低相关。AZD6244靶向抑制p-ERK可通过阻断血管生成抑制胃癌异种移植瘤生长且无全身毒性。AZD6244提供的抗血管生成作用可能归因于其对p-ERK - c-Fos - HIF-1α - VEGF整合信号通路的调节。