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白细胞介素-8 诱导的三阴性乳腺癌细胞侵袭实验。

Interleukin-8-Induced Invasion Assay in Triple-Negative Breast Cancer Cells.

机构信息

Department of Biological Sciences, St. John's University, Queens, NY, USA.

出版信息

Methods Mol Biol. 2020;2108:107-115. doi: 10.1007/978-1-0716-0247-8_9.

Abstract

The pro-inflammatory and pro-angiogenic chemokine interleukin-8 (IL-8, CXCL8) induces proliferation and invasion of solid tumor cells. In many types of solid cancer, including triple-negative breast cancer (TNBC), the IL-8 expression is induced by proteasome inhibition. In this chapter, we describe a protocol for the analysis of TNBC cell invasion induced by IL-8 in response to proteasome inhibition by bortezomib (BZ). Using this approach, we show that BZ increases the invasion ability of TNBC cells, and that the BZ-increased TNBC cell invasion is suppressed by IκB kinase (IKK) inhibition, which also decreases the IL-8 expression. The experimental protocol includes the cell invasion assay, microscopic evaluation of the invading cells, and quantitative analysis of the obtained images. This protocol should be applicable also for measurement of chemokine-induced tumor cell invasion in other types of cancer cells.

摘要

促炎和促血管生成的趋化因子白细胞介素-8(IL-8,CXCL8)可诱导实体瘤细胞的增殖和侵袭。在许多类型的实体瘤中,包括三阴性乳腺癌(TNBC),IL-8 的表达受蛋白酶体抑制诱导。在本章中,我们描述了一种分析由 IL-8 诱导的 TNBC 细胞侵袭的方案,该方案响应硼替佐米(BZ)对蛋白酶体的抑制。使用这种方法,我们表明 BZ 增加了 TNBC 细胞的侵袭能力,而 IκB 激酶(IKK)抑制可抑制 BZ 增加的 TNBC 细胞侵袭,同时降低 IL-8 的表达。该实验方案包括细胞侵袭实验、侵袭细胞的显微镜评估以及获得的图像的定量分析。该方案也可适用于测量其他类型癌细胞中趋化因子诱导的肿瘤细胞侵袭。

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