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整合素α6β4糖基化在癌症中的作用。

Roles of Integrin α6β4 Glycosylation in Cancer.

作者信息

Kariya Yoshinobu, Kariya Yukiko, Gu Jianguo

机构信息

Department of Biochemistry, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima City, Fukushima 960-1295, Japan.

Division of Regulatory Glycobiology, Institute of Molecular Biomembrane and Glycobiology, Tohoku Medical and Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai, Miyagi 981-8558, Japan.

出版信息

Cancers (Basel). 2017 Jul 5;9(7):79. doi: 10.3390/cancers9070079.

Abstract

Malignant transformation is accompanied with aberrant glycosylation of proteins. Such changes in glycan structure also occur in the integrins, which are a large family of cell surface receptors for the extracellular matrix and play key roles in tumor progression. There is now increasing evidence that glycosylation of integrins affects cellular signaling and interaction with the extracellular matrix, receptor tyrosine kinases, and galectins, thereby regulating cell adhesion, motility, growth, and survival. Integrin α6β4 is a receptor for laminin-332 and the increased expression level is correlated with malignant progression and poor survival in various types of cancers. Recent studies have revealed that integrin α6β4 plays central roles in tumorigenesis and the metastatic process. In this review, we summarize our current understanding of the molecular mechanisms of tumor progression driven by integrin α6β4 and also discuss the modification of glycans on integrin β4 subunit to address the important roles of glycan in integrin-mediated tumor progression.

摘要

恶性转化伴随着蛋白质的异常糖基化。聚糖结构的这种变化也发生在整合素中,整合素是细胞外基质的一大类细胞表面受体家族,在肿瘤进展中起关键作用。现在越来越多的证据表明,整合素的糖基化会影响细胞信号传导以及与细胞外基质、受体酪氨酸激酶和半乳糖凝集素的相互作用,从而调节细胞黏附、运动、生长和存活。整合素α6β4是层粘连蛋白-332的受体,其表达水平升高与各种类型癌症的恶性进展和不良预后相关。最近的研究表明,整合素α6β4在肿瘤发生和转移过程中起核心作用。在这篇综述中,我们总结了目前对整合素α6β4驱动肿瘤进展的分子机制的理解,并讨论了整合素β4亚基上聚糖的修饰,以阐述聚糖在整合素介导的肿瘤进展中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1938/5532615/91e6d923c1a8/cancers-09-00079-g001.jpg

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