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p73作为发育性血管生成调节因子的新作用:对癌症治疗的启示。

Novel role of p73 as a regulator of developmental angiogenesis: Implication for cancer therapy.

作者信息

Marin Maria C, Marques Margarita M

机构信息

Instituto de Biomedicina and Departmento de Biologia Molecular; University of Leon ; Leon, Spain.

Instituto de Desarrollo Ganadero; University of Leon ; Leon, Spain.

出版信息

Mol Cell Oncol. 2015 May 26;3(1):e1019973. doi: 10.1080/23723556.2015.1019973. eCollection 2016 Jan.

DOI:10.1080/23723556.2015.1019973
PMID:27308533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4845169/
Abstract

Information regarding the role of p73 in the regulation of angiogenesis has been incomplete and quite controversial. Remarkably, several groups, including ours, have recently demonstrated that TP73 plays a fundamental role in angiogenesis regulation and that differential expression of TP73 could have important consequences in tumor angiogenesis. Here, we discuss a possible model for p73 function in the regulation of developmental angiogenesis and tumor angiogenesis.

摘要

关于p73在血管生成调节中的作用的信息一直不完整且颇具争议。值得注意的是,包括我们在内的几个研究小组最近证明,TP73在血管生成调节中起基本作用,并且TP73的差异表达可能在肿瘤血管生成中产生重要影响。在此,我们讨论p73在发育性血管生成和肿瘤血管生成调节中的功能的一种可能模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0b/4845169/594cd8c86522/kmco-03-01-1019973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0b/4845169/594cd8c86522/kmco-03-01-1019973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0b/4845169/594cd8c86522/kmco-03-01-1019973-g001.jpg

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TAp73通过抑制促血管生成细胞因子和HIF-1α活性来抑制肿瘤血管生成。
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BMP4 Signaling Acts via dual-specificity phosphatase 9 to control ERK activity in mouse embryonic stem cells.BMP4 信号通过双特异性磷酸酶 9 作用来控制小鼠胚胎干细胞中的 ERK 活性。
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The hemangioblast: from concept to authentication.血岛细胞:从概念到证实。
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