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CXC趋化因子与血管生成/血管生成抑制

CXC chemokines and angiogenesis/angiostasis.

作者信息

Keane M P, Arenberg D A, Moore B B, Addison C L, Strieter R M

机构信息

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, USA.

出版信息

Proc Assoc Am Physicians. 1998 Jul-Aug;110(4):288-96.

PMID:9686676
Abstract

Angiogenesis is important to a variety of physiological and pathological processes. While a variety of factors have been determined to regulate angiogenesis, members of the CXC chemokine family can either promote or inhibit this process. This disparity in biological behavior is due to the presence or absence of a structural-functional domain--three amino acid residues (Glu-Leu-Arg: the "ELR-motif") that precede the first cysteine amino acid residue of the primary structure of these cytokines. The purpose of this study is to introduce the topic of angiogenesis and focuses on the CXC chemokine family, because these cytokines are a unique family of molecules that can behave in a disparate manner in the regulation of angiogenesis associated with either chronic inflammatory-fibroproliferative disorders or tumor growth.

摘要

血管生成对多种生理和病理过程都很重要。虽然已经确定多种因素可调节血管生成,但CXC趋化因子家族成员既能促进也能抑制这一过程。这种生物学行为的差异是由于这些细胞因子一级结构中第一个半胱氨酸氨基酸残基之前存在或不存在一个结构功能域——三个氨基酸残基(Glu-Leu-Arg:“ELR模体”)。本研究的目的是介绍血管生成这一主题,并聚焦于CXC趋化因子家族,因为这些细胞因子是一类独特的分子家族,在与慢性炎症性纤维增生性疾病或肿瘤生长相关的血管生成调节中表现出不同的行为。

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