Lasagna Nadia, Fantappiè Ornella, Solazzo Michela, Morbidelli Lucia, Marchetti Serena, Cipriani Greta, Ziche Marina, Mazzanti Roberto
Department of Internal Medicine, Postgraduate School in Oncology, DENOthe, University of Florence, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Cancer Res. 2006 Mar 1;66(5):2673-82. doi: 10.1158/0008-5472.CAN-05-2290.
Based on literature, it is possible to hypothesize that multidrug resistance (MDR) and angiogenic phenotypes are linked to each other in human liver cancer cells. Our goal is to assess whether MDR cells trigger angiogenesis and to study the possible molecular mechanisms involved. Conditioned medium from parental drug-sensitive P5 cells (P5-CM) and MDR-positive P1(0.5) cells [P1(0.5)-CM] stimulated human umbilical vein endothelial cells (HUVEC) survival, proliferation, migration, and microtubular structure formation, but P1(0.5)-CM had a significantly greater effect than P5-CM. Cell implants were done in the rabbit avascular cornea to measure angiogenesis in vivo: P1(0.5) cells induced an important neovascular response in rabbit cornea after 1 week, whereas P5 cells had no effect. P1(0.5) and P5 cells produced vascular endothelial growth factor, but only P1(0.5) secreted hepatocyte growth factor (HGF) into the medium, and small interfering RNA specific for MDR1 clearly reduced HGF production in P1(0.5) cells. The transcription factor Ets-1 and the HGF receptor c-Met were up-regulated in P1(0.5) cells and in HUVEC cultured in P1(0.5)-CM. Inducible nitric oxide synthase (iNOS) seemed to play a major role in the proangiogenic effect of P1(0.5), and its inhibition by 1400W blunted the capacity of P1(0.5) cells to stimulate HUVEC proliferation, migration, and Ets-1 expression. In conclusion, these data show that development of MDR and angiogenic phenotypes are linked to each other in MDR cells. HGF production, Ets-1 and c-Met up-regulation, and iNOS expression can be part of the molecular mechanisms that enhance the angiogenic activity of the MDR-positive hepatocellular carcinoma cell line.
基于文献,可以推测多药耐药(MDR)与血管生成表型在人肝癌细胞中相互关联。我们的目标是评估MDR细胞是否会引发血管生成,并研究其中可能涉及的分子机制。亲本药物敏感P5细胞的条件培养基(P5-CM)和MDR阳性P1(0.5)细胞的条件培养基[P1(0.5)-CM]均可刺激人脐静脉内皮细胞(HUVEC)的存活、增殖、迁移及微管结构形成,但P1(0.5)-CM的作用明显强于P5-CM。将细胞植入兔无血管角膜以测量体内血管生成:1周后,P1(0.5)细胞在兔角膜中诱导了显著的新生血管反应,而P5细胞则无此作用。P1(0.5)和P5细胞均产生血管内皮生长因子,但只有P1(0.5)向培养基中分泌肝细胞生长因子(HGF),而针对MDR1的小干扰RNA明显降低了P1(0.5)细胞中HGF的产生。转录因子Ets-1和HGF受体c-Met在P1(0.5)细胞以及在P1(0.5)-CM中培养的HUVEC中上调。诱导型一氧化氮合酶(iNOS)似乎在P1(0.5)的促血管生成作用中起主要作用,用1400W抑制iNOS可减弱P1(0.5)细胞刺激HUVEC增殖、迁移及Ets-1表达的能力。总之,这些数据表明MDR和血管生成表型在MDR细胞中相互关联。HGF的产生、Ets-1和c-Met的上调以及iNOS的表达可能是增强MDR阳性肝癌细胞系血管生成活性的分子机制的一部分。