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酸性微环境通过酸感应离子通道 1 诱导白细胞介素-8 表达和基质金属蛋白酶-2/-9 激活,促进乳腺癌细胞的进展。

Acidic microenvironment induction of interleukin-8 expression and matrix metalloproteinase-2/-9 activation via acid-sensing ion channel 1 promotes breast cancer cell progression.

机构信息

Department of Pathology, Wakayama Medical University, Wakayama 641-8509, Japan.

出版信息

Oncol Rep. 2021 Mar;45(3):1284-1294. doi: 10.3892/or.2020.7907. Epub 2020 Dec 24.

DOI:10.3892/or.2020.7907
PMID:33650662
Abstract

The cancer microenvironment exhibits local acidosis compared with the surrounding normal tissue. Many reports have shown that acidosis accelerates the invasiveness and metastasis of cancer, yet the underlying molecular mechanisms remain unclear. In the present study, we focused on acid-induced functional changes through acid receptors in breast cancer cells. Acidic treatment induced interleukin (IL)-8 expression in MDA-MB-231 cells and promoted cell migration and invasion. The acidic microenvironment elevated matrix metalloproteinase (MMP)-2 and MMP-9 activity, and addition of IL-8 had similar effects. However, inhibition of IL-8 suppressed the acid-induced migration and invasion of MDA-MB-231 cells. MDA-MB-231 cells express various acid receptors including ion channels and G protein-coupled receptors. Interestingly, acidic stimulation increased the expression of acid-sensing ion channel 1 (ASIC1), and acid-induced IL-8 was significantly decreased by ASIC1 knockdown. Moreover, phosphorylation of nuclear factor (NF)-κB was induced by acidic treatment, and inhibition of NF-κB activation reduced acid-induced IL-8 expression. These results suggest that IL-8 induction by an acidic microenvironment promotes breast cancer development and that ASIC1 might be a novel therapeutic target for breast cancer metastasis.

摘要

与周围正常组织相比,癌症微环境表现出局部酸中毒。许多报告表明,酸中毒加速了癌症的侵袭和转移,但潜在的分子机制仍不清楚。在本研究中,我们专注于通过乳腺癌细胞中的酸受体研究酸诱导的功能变化。酸性处理诱导 MDA-MB-231 细胞中白细胞介素(IL)-8 的表达,并促进细胞迁移和侵袭。酸性微环境升高了基质金属蛋白酶(MMP)-2 和 MMP-9 的活性,添加 IL-8 也具有类似的作用。然而,抑制 IL-8 抑制了 MDA-MB-231 细胞的酸诱导迁移和侵袭。MDA-MB-231 细胞表达多种酸受体,包括离子通道和 G 蛋白偶联受体。有趣的是,酸性刺激增加了酸敏感离子通道 1(ASIC1)的表达,并且 ASIC1 敲低显著降低了酸诱导的 IL-8。此外,酸性处理诱导核因子(NF)-κB 的磷酸化,抑制 NF-κB 激活可减少酸诱导的 IL-8 表达。这些结果表明,酸性微环境诱导的 IL-8 促进乳腺癌的发展,ASIC1 可能是乳腺癌转移的一个新的治疗靶点。

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