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KH 型剪接调控蛋白控制结直肠癌细胞生长并调节肿瘤微环境。

KH-Type Splicing Regulatory Protein Controls Colorectal Cancer Cell Growth and Modulates the Tumor Microenvironment.

机构信息

Centre for Colorectal Disease, St. Vincent's University Hospital, Dublin, Ireland; Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California.

Centre for Colorectal Disease, St. Vincent's University Hospital, Dublin, Ireland; School of Medicine, University College Dublin, Dublin, Ireland.

出版信息

Am J Pathol. 2019 Oct;189(10):1916-1932. doi: 10.1016/j.ajpath.2019.07.004. Epub 2019 Aug 9.

Abstract

KH-type splicing regulatory protein (KHSRP) is a multifunctional nucleic acid binding protein implicated in key aspects of cancer cell biology: inflammation and cell-fate determination. However, the role KHSRP plays in colorectal cancer (CRC) tumorigenesis remains largely unknown. Using a combination of in silico analysis of large data sets, ex vivo analysis of protein expression in patients, and mechanistic studies using in vitro models of CRC, we investigated the oncogenic role of KHSRP. We demonstrated KHSRP expression in the epithelial and stromal compartments of both primary and metastatic tumors. Elevated expression was found in tumor versus matched normal tissue, and these findings were validated in larger independent cohorts in silico. KHSRP expression was a prognostic indicator of worse overall survival (hazard ratio, 3.74; 95% CI, 1.43-22.97; P = 0.0138). Mechanistic data in CRC cell line models supported a role of KHSRP in driving epithelial cell proliferation in both a primary and metastatic setting, through control of the G/S transition. In addition, KHSRP promoted a proangiogenic extracellular environment by regulating the secretion of oncogenic proteins involved in diverse cellular processes, such as migration and response to cellular stress. Our study provides novel mechanistic insight into the tumor-promoting effects of KHSRP in CRC.

摘要

KH 型剪接调控蛋白 (KHSRP) 是一种多功能核酸结合蛋白,与癌细胞生物学的关键方面有关:炎症和细胞命运决定。然而,KHSRP 在结直肠癌 (CRC) 肿瘤发生中的作用在很大程度上尚不清楚。我们使用计算机分析大型数据集、对患者的蛋白质表达进行体外分析,以及使用 CRC 的体外模型进行机制研究的组合,研究了 KHSRP 的致癌作用。我们证明了 KHSRP 在原发性和转移性肿瘤的上皮和基质区室中的表达。在肿瘤与匹配的正常组织中发现表达升高,这些发现通过计算机模拟在更大的独立队列中得到了验证。KHSRP 表达是总体生存不良的预后指标(危险比,3.74;95%置信区间,1.43-22.97;P = 0.0138)。CRC 细胞系模型中的机制数据支持 KHSRP 在原发性和转移性环境中通过控制 G/S 过渡来驱动上皮细胞增殖的作用。此外,KHSRP 通过调节参与多种细胞过程(如迁移和对细胞应激的反应)的致癌蛋白的分泌,促进了促血管生成的细胞外环境。我们的研究为 KHSRP 在 CRC 中的促肿瘤作用提供了新的机制见解。

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