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Silencing the hsp25 Gene Eliminates Migration Capability of the Highly Metastatic Murine 4T1 Breast Adenocarcinoma Cell

机译:沉默hsp25基因消除了高度转移性小鼠4T1乳腺癌细胞的迁移能力。

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摘要

The 25-kDa heat shock protein (Hsp25) is associated with various malignancies and is expressed at high levels in biopsies as well as circulating in the serum of breast cancer patients. In this study, we used RNA interference technology to silence the hsp25 gene in 4T1 breast adenocarcinoma cells, known as a poorly immunogenic, highly metastatic cell line. We demonstrate that transfection of 4T1 cells with short interference RNA-Hsp25 dramatically inhibits proliferation as compared with control transfected cells. In addition, we show that 4T1 cells transfected with short interference RNA-Hsp25 abrogates tumor migration potential by a mechanism that is in part due to the repression of matrix metalloproteinase 9 expression and a concomitant upregulation of its antagonist, tissue inhibitor metalloproteinase 1. Taken together, these findings provide a model system for the study of metastatic potential of tumors and are suggestive of an earlier unrecognized role for Hsp25 in tumor migration.
机译:25 kDa热激蛋白(Hsp25)与各种恶性肿瘤相关,并在活检组织中高水平表达,并在乳腺癌患者的血清中循环表达。在这项研究中,我们使用RNA干扰技术来沉默4T1乳腺癌细胞中的hsp25基因,该细胞被称为免疫原性差,高度转移性细胞系。我们证明,与对照转染细胞相比,短干扰RNA-Hsp25转染4T1细胞可显着抑制增殖。此外,我们显示,短干扰RNA-Hsp25转染的4T1细胞通过某种机制消除了肿瘤的迁移潜力,该机制部分归因于基质金属蛋白酶9表达的抑制及其拮抗剂组织抑制剂金属蛋白酶1的上调。 ,这些发现为研究肿瘤的转移潜力提供了一个模型系统,并暗示了Hsp25在肿瘤迁移中的较早未被认识的作用。

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