Department of Surgery, UCL Division of Surgery and Interventional Science, London, United Kingdom.
Int J Cancer. 2012 Mar 15;130(6):1264-72. doi: 10.1002/ijc.26090. Epub 2011 Jun 9.
Endothelin-1 (ET-1) is produced by and stimulates colorectal cancer cells. Fibroblasts produce tumour stroma required for cancer development. We investigated whether ET-1 stimulated processes involved in tumour stroma production by colonic fibroblasts. Primary human fibroblasts, isolated from normal tissues adjacent to colon cancers, were cultured with or without ET-1 and its antagonists. Cellular proliferation, migration and contraction were measured. Expression of enzymes involved in tumour stroma development and alterations in gene transcription were determined by Western blotting and genome microarrays. ET-1 stimulated proliferation, contraction and migration (p < 0.01 v control) and the expression of matrix degrading enzymes TIMP-1 and MMP-2, but not MMP-3. ET-1 upregulated genes for profibrotic growth factors and receptors, signalling molecules, actin modulators and extracellular matrix components. ET-1 stimulated colonic fibroblast cellular processes in vitro that are involved in developing tumour stroma. Upregulated genes were consistent with these processes. By acting as a strong stimulus for tumour stroma creation, ET-1 is proposed as a target for adjuvant cancer therapy.
内皮素-1(ET-1)由结直肠癌细胞产生并刺激其生长。成纤维细胞产生肿瘤生长所需的基质。我们研究了 ET-1 是否刺激结直肠成纤维细胞产生肿瘤基质的过程。原代人结直肠成纤维细胞取自结肠癌旁的正常组织,在有无 ET-1 及其拮抗剂的条件下进行培养。通过细胞增殖、迁移和收缩试验来测量细胞的增殖、迁移和收缩。通过 Western blot 和基因芯片检测肿瘤基质形成中涉及的酶的表达和基因转录的改变。ET-1 刺激增殖、收缩和迁移(p < 0.01 比对照组)以及基质降解酶 TIMP-1 和 MMP-2 的表达,但不包括 MMP-3。ET-1 上调了致纤维化生长因子及其受体、信号分子、肌动蛋白调节剂和细胞外基质成分的基因。ET-1 在体外刺激结直肠成纤维细胞的细胞过程,这些过程参与了肿瘤基质的形成。上调的基因与这些过程一致。ET-1 作为肿瘤基质形成的强刺激物,被提议作为辅助癌症治疗的靶点。