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基于iTRAQ的多倍体巨癌细胞和出芽子代细胞蛋白质组学分析揭示了卵巢癌发展的几种不同途径。

iTRAQ-based proteomic analysis of polyploid giant cancer cells and budding progeny cells reveals several distinct pathways for ovarian cancer development.

作者信息

Zhang Shiwu, Mercado-Uribe Imelda, Hanash Samir, Liu Jinsong

机构信息

Department of Pathology, Tianjin Union Medicine Center (Nankai University Affiliated Hospital), Tianjin, People's Republic of China ; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.

出版信息

PLoS One. 2013 Nov 14;8(11):e80120. doi: 10.1371/journal.pone.0080120. eCollection 2013.

Abstract

Polyploid giant cancer cells (PGCCs) are a morphologically distinct subgroup of human tumor cells with increased nuclear size or multiple nuclei, but they are generally considered unimportant because they are presumed to be nondividing and thus nonviable. We have recently shown that these large cancer cells are not only viable but also can divide asymmetrically and yield progeny cancer cells with cancer stem-like properties via budding division. To further understand the molecular events involved in the regulation of PGCCs and the generation of their progeny cancer cells, we comparatively analyzed the proteomic profiles of PGCCs, PGCCs with budding daughter cells, and regular control cancer cells from the HEY and SKOv3 human ovarian cancer cell lines with and without CoCl2. We used a high-throughput iTRAQ-based proteomic methodology coupled with liquid chromatography-electrospray ionization tandem mass spectroscopy to determine the differentiated regulated proteins. We performed Western blotting and immunohistochemical analyses to validate the differences in the expression patterns of a variety of proteins between PGCCs or budding PGCCs and regular cancer cells identified by iTRAQ approach and also a selected group of proteins from the literature. The differentially regulated proteins included proteins involved in response to hypoxia, stem cell generation, chromatin remodeling, cell-cycle regulation, and invasion and metastasis. In particular, we found that HIF-1alpha and its known target STC1 are upregulated in PGCCs. In addition, we found that a panel of stem cell-regulating factors and epithelial-to-mesenchymal transition regulatory transcription factors were upregulated in budding PGCCs, whereas expression of the histone 1 family of nucleosomal linker proteins was consistently lower in PGCCs than in control cells. Thus, proteomic expression patterns provide valuable insight into the underlying mechanisms of PGCC formation and the relationship between PGCCs and cancer stem cells in patients with ovarian cancers.

摘要

多倍体巨癌细胞(PGCCs)是人类肿瘤细胞中形态上独特的一个亚群,其细胞核增大或有多个细胞核,但通常被认为不重要,因为它们被假定为不分裂,因此无活力。我们最近发现,这些大癌细胞不仅有活力,而且能够不对称分裂,并通过出芽分裂产生具有癌症干细胞样特性的子代癌细胞。为了进一步了解参与PGCCs调控及其子代癌细胞生成的分子事件,我们比较分析了来自HEY和SKOv3人卵巢癌细胞系的PGCCs、带有出芽子代细胞的PGCCs以及正常对照癌细胞在有或没有CoCl2情况下的蛋白质组学图谱。我们使用基于iTRAQ的高通量蛋白质组学方法结合液相色谱 - 电喷雾电离串联质谱来确定差异调节的蛋白质。我们进行了蛋白质印迹和免疫组织化学分析,以验证通过iTRAQ方法鉴定的PGCCs或出芽PGCCs与正常癌细胞之间多种蛋白质表达模式的差异,以及从文献中选取的一组蛋白质的差异。差异调节的蛋白质包括参与缺氧反应、干细胞生成、染色质重塑、细胞周期调控以及侵袭和转移的蛋白质。特别地,我们发现HIF - 1α及其已知靶点STC1在PGCCs中上调。此外,我们发现一组干细胞调节因子和上皮 - 间质转化调节转录因子在出芽PGCCs中上调,而核小体连接蛋白的组蛋白1家族在PGCCs中的表达始终低于对照细胞。因此,蛋白质组学表达模式为卵巢癌患者中PGCCs形成的潜在机制以及PGCCs与癌症干细胞之间的关系提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0b/3858113/86bef6021180/pone.0080120.g001.jpg

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