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巢蛋白与组织损伤和癌症的关系——一种潜在的肿瘤标志物?

Nestin involvement in tissue injury and cancer--a potential tumor marker?

作者信息

Tampaki Ekaterini Christina, Nakopoulou Lydia, Tampakis Athanasios, Kontzoglou Konstantinos, Weber Walter P, Kouraklis Gregory

机构信息

2nd Department of Propedeutic Surgery, Athens University Medical School, Laiko General Hospital, 17 Agiou Thoma Street, 11527, Athens, Greece,

出版信息

Cell Oncol (Dordr). 2014 Oct;37(5):305-15. doi: 10.1007/s13402-014-0193-5. Epub 2014 Aug 28.

Abstract

BACKGROUND

In eukaryotic cells, the cytoskeleton contains three major filamentous components: actin microfilaments, microtubules and intermediate filaments. Nestin represents one of the class VI intermediate filament proteins. Clinical and molecular analyses have revealed substantial information regarding the presence of Nestin in cells with progenitor or stem cell properties. During tissue injury Nestin is expressed in cells with progenitor cell-like properties. These cells may serve as a tissue reserve and, as such, may contribute to tissue repair. Based on currently available data, Nestin also appears to be implicated in two oncogenic processes. First, Nestin has been found to be expressed in cancer stem-like cells and poorly differentiated cancer cells and, as such, Nestin is thought to contribute to the aggressive behavior of these cells. Second, Nestin has been found to be involved in tumor angiogenesis through an interaction of cancer cells and blood vessel endothelial cells and, as such, Nestin is thought to facilitate tumor growth.

CONCLUSIONS

We conclude that Nestin may serve as a promising tumor marker and as a potential therapeutic target amenable to tumor suppression and angiogenesis inhibition.

摘要

背景

在真核细胞中,细胞骨架包含三种主要的丝状成分:肌动蛋白微丝、微管和中间丝。巢蛋白是VI类中间丝蛋白之一。临床和分子分析已经揭示了关于巢蛋白在具有祖细胞或干细胞特性的细胞中存在的大量信息。在组织损伤期间,巢蛋白在具有祖细胞样特性的细胞中表达。这些细胞可能作为一种组织储备,因此可能有助于组织修复。基于目前可用的数据,巢蛋白似乎也与两种致癌过程有关。首先,已发现巢蛋白在癌症干细胞样细胞和低分化癌细胞中表达,因此,巢蛋白被认为促成了这些细胞的侵袭性。其次,已发现巢蛋白通过癌细胞与血管内皮细胞的相互作用参与肿瘤血管生成,因此,巢蛋白被认为促进肿瘤生长。

结论

我们得出结论,巢蛋白可能作为一种有前景的肿瘤标志物以及作为一个适合肿瘤抑制和血管生成抑制的潜在治疗靶点。

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