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Nm23与肿瘤抑制因子VHL之间的相互作用。

Interaction between Nm23 and the tumor suppressor VHL.

作者信息

Lin Chih-Hung, Dammai Vincent, Adryan Boris, Hsu Tien

机构信息

Department of Surgery, Cathay General Hospital, Taipei, Taiwan, Republic of China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2015 Feb;388(2):143-52. doi: 10.1007/s00210-014-1002-4. Epub 2014 Jun 12.

Abstract

Among the anti-tumor genes (tumor suppressors and metastasis suppressors), the von-Hippel Lindau gene and the Nm23 family of genes are among the more intriguing ones. Both are small (long and short forms of VHL are 30 and 19 kD, respectively, and Nm23 is ~17 kD), and both possess diverse molecular and cellular functions. Despite extensive studies, the entire spectra of functions and the molecular function-phenotype correlation of these two proteins have not been completely elucidated. In this report, we present data showing these two proteins interact physically. We also summarize and confirm the previous studies that demonstrated the endocytic function of these two genes and further show that the endocytic function of VHL is mediated through the activity of Nm23. These functional and molecular interactions are evolutionarily conserved from Drosophila to human.

摘要

在抗肿瘤基因(肿瘤抑制基因和转移抑制基因)中,冯·希佩尔-林道基因和Nm23基因家族是比较引人关注的。二者都很小(VHL的长、短形式分别为30 kD和19 kD,Nm23约为17 kD),且都具有多种分子和细胞功能。尽管进行了广泛研究,但这两种蛋白质的全部功能谱以及分子功能与表型的相关性尚未完全阐明。在本报告中,我们展示的数据表明这两种蛋白质存在物理相互作用。我们还总结并证实了先前证明这两个基因具有内吞功能的研究,并进一步表明VHL的内吞功能是通过Nm23的活性介导的。这些功能和分子相互作用从果蝇到人类在进化上是保守的。

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