Le Jan Sébastien, Amy Céline, Cazes Aurélie, Monnot Catherine, Lamandé Noël, Favier Judith, Philippe Josette, Sibony Mathilde, Gasc Jean-Marie, Corvol Pierre, Germain Stéphane
INSERM U36, Collège de France, Paris.
Am J Pathol. 2003 May;162(5):1521-8. doi: 10.1016/S0002-9440(10)64285-X.
Ischemic and solid tumor tissues are less well perfused than normal tissue, leading to metabolic changes and chronic hypoxia, which in turn promotes angiogenesis. We identified human angiopoietin-like 4 (angptl4) as a gene with hypoxia-induced expression in endothelial cells. We showed that the levels of both mRNA and protein for ANGPTL4 increased in response to hypoxia. When tested in the chicken chorioallantoic membrane assay, ANGPTL4 induced a strong proangiogenic response, independently of vascular endothelial growth factor. In human pathology, ANGPTL4 mRNA is produced in ischemic tissues, in conditions such as critical leg ischemia. In tumors, ANGPTL4 is produced in the hypoxic areas surrounding necrotic regions. We observed particularly high levels of ANGPTL4 mRNA in tumor cells of conventional renal cell carcinoma. Other benign and malignant renal tumor cells do not produce ANGPTL4 mRNA. This molecule therefore seems to be a marker of conventional renal cell carcinoma. ANGPTL4, originally identified as a peroxisome proliferator-activated receptor alpha and gamma target gene, has potential for use as a new diagnostic tool and a potential therapeutic target, modulating angiogenesis both in tumors and in ischemic tissues. This study also suggests that ANGPTL4 may provide a link between metabolic disorders and hypoxia-induced angiogenesis.
与正常组织相比,缺血组织和实体瘤组织的灌注较差,导致代谢变化和慢性缺氧,进而促进血管生成。我们鉴定出人类血管生成素样4(angptl4)是一种在内皮细胞中受缺氧诱导表达的基因。我们发现,缺氧会导致ANGPTL4的mRNA和蛋白质水平升高。在鸡胚绒毛尿囊膜试验中进行测试时,ANGPTL4可诱导强烈的促血管生成反应,且不依赖于血管内皮生长因子。在人类病理学中,ANGPTL4 mRNA在诸如严重下肢缺血等缺血组织中产生。在肿瘤中,ANGPTL4在坏死区域周围的缺氧区域产生。我们在传统肾细胞癌的肿瘤细胞中观察到特别高水平的ANGPTL4 mRNA。其他良性和恶性肾肿瘤细胞不产生ANGPTL4 mRNA。因此,该分子似乎是传统肾细胞癌的标志物。ANGPTL4最初被鉴定为过氧化物酶体增殖物激活受体α和γ的靶基因,具有用作新诊断工具和潜在治疗靶点的潜力,可调节肿瘤和缺血组织中的血管生成。这项研究还表明,ANGPTL4可能在代谢紊乱和缺氧诱导的血管生成之间提供联系。