首页> 外文期刊>Molecular cancer research: MCR >Vitamin k epoxide reductase: a protein involved in angiogenesis.
【24h】

Vitamin k epoxide reductase: a protein involved in angiogenesis.

机译:维生素K环氧还原酶:一种参与血管生成的蛋白质。

获取原文
获取原文并翻译 | 示例
           

摘要

Vitamin K epoxide reductase (VKOR) is a newly identified protein which has been reported to convert the epoxide of vitamin K back to vitamin K, a cofactor essential for the posttranslational gamma-carboxylation of several blood coagulation factors. We found that the gene is expressed ubiquitously including vascular endothelial cells, smooth muscle cells, fibroblasts and cardiomyocytes, and is overexpressed in 11 tumor tissues on microarray. Stable transfection of VKOR cDNA into tumor cell line A549 and H7402 did not promote the cell proliferation. These results promoted us to hypothesize that VKOR may also be involved in angiogenesis. To test this hypothesis, the expression of VKOR was studied in different vascular cells in developmental and pathologic heart tissues. The effects of overexpression and suppressing expression of VKOR on endothelial cell proliferation, migration, adhesion, and tubular network formation were explored. We found that VKOR expression in arteries was prominent in vascular endothelial cells and was high in the ventricular aneurysm tissue of human heart and human fetal heart. In vitro studies showed that overexpression of VKOR slightly but significantly stimulated human umbilical vein endothelial cell proliferation (by 120%), migration (by 118%), adhesion (by 117%), as well as tubular network formation. Antisense to VKOR gene inhibited the proliferation (by 67%), migration (by 64%), adhesion (by 50%), and tubular network formation. Our findings support the impact of VKOR in the process of angiogenesis; hence, the molecule may have a potential application in cardiovascular disease and cancer therapy.
机译:维生素K环氧还原酶(VKOR)是一种新近鉴定的蛋白质,据报道可将维生素K的环氧化物转化回维生素K,这是几种凝血因子的翻译后γ-羧化所必需的辅因子。我们发现该基因广泛表达,包括血管内皮细胞,平滑肌细胞,成纤维细胞和心肌细胞,并且在微阵列上的11个肿瘤组织中过表达。 VKOR cDNA稳定转染到肿瘤细胞系A549和H7402中不会促进细胞增殖。这些结果促使我们推测VKOR也可能与血管生成有关。为了验证该假设,研究了发育和病理性心脏组织中不同血管细胞中VKOR的表达。探索过表达和抑制VKOR表达对内皮细胞增殖,迁移,粘附和肾小管网络形成的影响。我们发现,血管中的VKOR表达在血管内皮细胞中突出,在人心脏和胎儿心脏的心室动脉瘤组织中高表达。体外研究表明,VKOR的过表达轻微但显着刺激了人脐静脉内皮细胞的增殖(120%),迁移(118%),粘附(117%)以及肾小管网络形成。对VKOR基因的反义抑制增殖(67%),迁移(64%),粘附(50%)和肾小管网络形成。我们的发现支持了VKOR在血管生成过程中的影响。因此,该分子可能在心血管疾病和癌症治疗中具有潜在的应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号