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PHD2 在肿瘤血管生成中。

PHD2 in tumour angiogenesis.

机构信息

Department of Radiation Oncology, University of California, 2340 Sutter Street, S-332, Box 1331, San Francisco, CA 94143-1331, USA.

出版信息

Br J Cancer. 2010 Jun 29;103(1):1-5. doi: 10.1038/sj.bjc.6605682. Epub 2010 May 11.

Abstract

Originally identified as the enzymes responsible for catalysing the oxidation of specific, conserved proline residues within hypoxia-inducible factor-1alpha (HIF-1alpha), the additional roles for the prolyl hydroxylase domain (PHD) proteins have remained elusive. Of the four identified PHD enzymes, PHD2 is considered to be the key oxygen sensor, as knockdown of PHD2 results in elevated HIF protein. Several recent studies have highlighted the importance of PHD2 in tumourigenesis. However, there is conflicting evidence as to the exact role of PHD2 in tumour angiogenesis. The divergence seems to be because of the contribution of stromal-derived PHD2, and in particular the involvement of endothelial cells, vs tumour-derived PHD2. This review summarises our current understanding of PHD2 and tumour angiogenesis, focusing on the influences of PHD2 on vascular normalisation and neovascularisation.

摘要

最初被确定为催化缺氧诱导因子-1α(HIF-1α)中特定保守脯氨酸残基氧化的酶,脯氨酰羟化酶结构域(PHD)蛋白的其他作用仍然难以捉摸。在四种已鉴定的 PHD 酶中,PHD2 被认为是关键的氧传感器,因为 PHD2 的敲低会导致 HIF 蛋白升高。最近的几项研究强调了 PHD2 在肿瘤发生中的重要性。然而,关于 PHD2 在肿瘤血管生成中的确切作用存在相互矛盾的证据。这种分歧似乎是由于基质衍生的 PHD2 的贡献,特别是内皮细胞的参与,而不是肿瘤衍生的 PHD2。这篇综述总结了我们目前对 PHD2 和肿瘤血管生成的理解,重点介绍了 PHD2 对血管正常化和新血管生成的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3119/2905285/c1afdf0a7af9/6605682f1.jpg

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