Seo Ju Hyeon, Jung Kyung Hee, Son Mi Kwon, Yan Hong Hua, Ryu Ye-Lim, Kim Jinhee, Lee Jung Kyun, Hong Sungwoo, Hong Soon-Sun
Department of Drug Development, College of Medicine, Inha University, 3-ga, Sinheung-dong, Jung-gu, Incheon 400-712, Republic of Korea.
Cancer Lett. 2013 Sep 28;338(2):271-81. doi: 10.1016/j.canlet.2013.04.002. Epub 2013 Apr 13.
Tropomyosin-related kinase A (TrkA) is emerging as an important player in carcinogenic progression. TrkA overexpression, which is associated with cell growth, proliferation, survival, and invasion, has been observed in pancreatic cancer. We therefore synthesized HS-345, a novel TrkA inhibitor, and evaluated its anti-cancer effect and underlying mechanism of action in pancreatic cancer. In this study, HS-345 effectively inhibited the growth and proliferation in three pancreatic cancer cell lines (PANC-1, MIA PaCa-2, and BxPC-3). Activation of the TrkA/Akt signal cascade was also inhibited by HS-345 treatment in a dose-dependent manner. The pro-apoptotic effect of HS-345 was evidenced by increased levels of cleaved caspase-3 and cleaved PARP, and decrease of Bcl/Bax expression via mitochondria membrane potential, as well as elevated numbers of TUNEL-positive apoptotic cells. HS-345 was additionally found to exert anti-angiogenic effect by decreasing the expression of HIF-1α and VEGF, major factors of angiogenesis, which were also demonstrated by the suppression of tube formation and migration of VEGF-treated human umbilical vein endothelial cells along with inhibition of blood vessel formation by HS-345 in a Matrigel plug assay with mice. Results of our investigation show that HS-345 inhibited the TrkA/Akt signaling pathway resulting in cell growth/angiogenesis inhibition and apoptosis induction. Based on our data, we suggest that HS-345 is a potential candidate for treating pancreatic cancer.
原肌球蛋白相关激酶A(TrkA)在致癌进程中逐渐成为一个重要角色。在胰腺癌中已观察到TrkA过表达,其与细胞生长、增殖、存活及侵袭相关。因此,我们合成了一种新型TrkA抑制剂HS - 345,并评估了其在胰腺癌中的抗癌作用及潜在作用机制。在本研究中,HS - 345有效抑制了三种胰腺癌细胞系(PANC - 1、MIA PaCa - 2和BxPC - 3)的生长和增殖。HS - 345处理还以剂量依赖性方式抑制了TrkA/Akt信号级联的激活。HS - 345的促凋亡作用通过裂解的半胱天冬酶 - 3和裂解的聚(ADP - 核糖)聚合酶水平升高、通过线粒体膜电位导致的Bcl/Bax表达降低以及TUNEL阳性凋亡细胞数量增加得以证明。此外,发现HS - 345通过降低血管生成的主要因子HIF - 1α和VEGF的表达发挥抗血管生成作用,这也通过抑制VEGF处理的人脐静脉内皮细胞的管形成和迁移以及在小鼠基质胶栓试验中HS - 345抑制血管形成得以证实。我们的研究结果表明,HS - 345抑制TrkA/Akt信号通路,导致细胞生长/血管生成抑制和凋亡诱导。基于我们的数据,我们认为HS - 345是治疗胰腺癌的潜在候选药物。