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内皮素-1 通过促进基质-上皮相互作用刺激头颈部鳞状细胞癌的运动性。

Endothelin-1 stimulates motility of head and neck squamous carcinoma cells by promoting stromal-epithelial interactions.

机构信息

Oral Disease Research Group, School of Clinical Dentistry, University of Sheffield S10 2TA, UK.

出版信息

Int J Cancer. 2012 Jan 1;130(1):40-7. doi: 10.1002/ijc.25968. Epub 2011 Apr 13.

Abstract

The invasion and migration of cancer cells is increasingly recognised to be influenced by factors derived from adjacent tumour-associated stroma. The contextual signals regulating stromal-tumour interactions, however, remain poorly understood. Here, we identify a role for endothelin-1 (ET-1), a mitogenic peptide elevated in a number of malignancies, in promoting pro-metastatic cross-talk between head and neck cancer cells and adjacent fibroblasts. We demonstrate that treatment of oral fibroblasts with ET-1 activates ADAM17-mediated release of epidermal growth factor receptor (EGFR) ligands, triggering EGFR signalling and increased motility in neighbouring head and neck cancer cells. ET-1-mediated paracrine transactivation of EGFR also increased cyclo-oxygenase-2 levels in the cancer cells, providing a molecular insight into the mechanisms by which the elevated levels of ET-1 observed in head and neck cancers may contribute to disease progression.

摘要

癌细胞的侵袭和迁移越来越被认为受到来自肿瘤相关基质的相关因素的影响。然而,调节基质-肿瘤相互作用的上下文信号仍知之甚少。在这里,我们确定内皮素-1(ET-1)在促进头颈部癌细胞和相邻成纤维细胞之间的促转移交叉对话中发挥作用,ET-1 是一种在多种恶性肿瘤中升高的有丝分裂肽。我们证明,用 ET-1 处理口腔成纤维细胞可激活 ADAM17 介导的表皮生长因子受体(EGFR)配体的释放,从而触发相邻头颈部癌细胞中的 EGFR 信号和迁移增加。ET-1 介导的 EGFR 旁分泌转激活也增加了癌细胞中环氧化酶-2 的水平,为观察到头颈部癌症中升高的 ET-1 水平可能导致疾病进展的机制提供了分子见解。

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