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内源性 GRP78 相互作用组在人类头颈部癌症中的作用:细胞表面 GRP78 在癌症干性中的决定性作用。

The Endogenous GRP78 Interactome in Human Head and Neck Cancers: A Deterministic Role of Cell Surface GRP78 in Cancer Stemness.

机构信息

Graduate Institute of Biomedical Sciences, Chang Gung University College of Medicine, Tao-Yuan, Taiwan.

Department of Radiation Oncology, Chang Gung Memorial Hospital, Tao-Yuan, Taiwan.

出版信息

Sci Rep. 2018 Jan 11;8(1):536. doi: 10.1038/s41598-017-14604-5.

Abstract

Cell surface glucose regulated protein 78 (GRP78), an endoplasmic reticulum (ER) chaperone, was suggested to be a cancer stem cell marker, but the influence of this molecule on cancer stemness is poorly characterized. In this study, we developed a mass spectrometry platform to detect the endogenous interactome of GRP78 and investigated its role in cancer stemness. The interactome results showed that cell surface GRP78 associates with multiple molecules. The influence of cell population heterogeneity of head and neck cancer cell lines (OECM1, FaDu, and BM2) according to the cell surface expression levels of GRP78 and the GRP78 interactome protein, Progranulin, was investigated. The four sorted cell groups exhibited distinct cell cycle distributions, asymmetric/symmetric cell divisions, and different relative expression levels of stemness markers. Our results demonstrate that cell surface GRP78 promotes cancer stemness, whereas drives cells toward a non-stemlike phenotype when it chaperones Progranulin. We conclude that cell surface GRP78 is a chaperone exerting a deterministic influence on cancer stemness.

摘要

细胞表面葡萄糖调节蛋白 78(GRP78)是内质网(ER)伴侣蛋白,被认为是癌症干细胞标志物,但该分子对癌症干细胞特性的影响尚未得到充分描述。在这项研究中,我们开发了一种质谱平台来检测 GRP78 的内源性互作组,并研究了它在癌症干细胞特性中的作用。互作组结果表明,细胞表面的 GRP78 与多种分子结合。根据 GRP78 表面表达水平和 GRP78 互作蛋白颗粒蛋白前体(Progranulin),研究了头颈部癌细胞系(OECM1、FaDu 和 BM2)细胞群体异质性的影响。四个分选的细胞群表现出不同的细胞周期分布、不对称/对称细胞分裂以及不同的干性标志物相对表达水平。我们的结果表明,细胞表面的 GRP78 促进了癌症干细胞特性,而当它伴侣蛋白 Progranulin 时,会促使细胞向非干细胞样表型分化。我们得出结论,细胞表面的 GRP78 是一种伴侣蛋白,对癌症干细胞特性具有决定性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f3a/5765009/81c9091f74ad/41598_2017_14604_Fig1_HTML.jpg

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