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粒细胞巨噬细胞集落刺激因子上调人头颈部癌细胞中的基质金属蛋白酶-2(MMP-2)和膜型1基质金属蛋白酶(MT1-MMP)。

Granulocyte-macrophage colony-stimulating factor upregulates matrix metalloproteinase-2 (MMP-2) and membrane type-1 MMP (MT1-MMP) in human head and neck cancer cells.

作者信息

Tomita T, Fujii M, Tokumaru Y, Imanishi Y, Kanke M, Yamashita T, Ishiguro R, Kanzaki J, Kameyama K, Otani Y

机构信息

Department of Otolaryngology, Keio University, School of Medicine, 35 Shinanomachi, Shinjuku-ku, 160-8582, Tokyo, Japan.

出版信息

Cancer Lett. 2000 Aug 1;156(1):83-91. doi: 10.1016/s0304-3835(00)00446-8.

Abstract

Matrix metalloproteinase-2 (MMP-2) and membrane type 1-MMP (MT1-MMP) play an important role in the invasion and metastasis of head and neck squamous cell carcinoma (HNSCC), but the mechanism of their regulation is not clearly understood. Recently, granulocyte-macrophage colony-stimulating factor (GM-CSF) has been shown to be associated with cancer invasion and metastasis. We hypothesized that GM-CSF may upregulate MMP-2 and/or MT1-MMP expression in HNSCC cells, and may thereby influence their ability to invade and metastasize. We studied the effects of GM-CSF on the production of MMP-2 and MT1-MMP in HNSCC cell lines SAS and HSC-2. Gelatin zymography of conditioned media derived from HNSCC cells revealed a major band of 68 kDa, which was characterized as proMMP-2. GM-CSF stimulated the production of proMMP-2 in both cell lines in a dose-dependent manner. Treatment with 50 ng/ml GM-CSF for 24 h increased the proMMP-2 activity 3.4-fold in SAS cells and 2.3-fold in HSC-2 cells compared with untreated controls. Northern blot analyses demonstrated that GM-CSF led to elevated mRNA levels of MMP-2 and MT1-MMP in both cell lines. The results identify GM-CSF as a regulator of MMP-2 and MT1-MMP expression in certain types of HNSCC, and suggest that GM-CSF may contribute to the invasiveness of HNSCC through the regulation of MMP-2 and MT1-MMP expression.

摘要

基质金属蛋白酶-2(MMP-2)和膜型1基质金属蛋白酶(MT1-MMP)在头颈部鳞状细胞癌(HNSCC)的侵袭和转移中起重要作用,但其调控机制尚不清楚。最近,粒细胞-巨噬细胞集落刺激因子(GM-CSF)已被证明与癌症侵袭和转移有关。我们假设GM-CSF可能上调HNSCC细胞中MMP-2和/或MT1-MMP的表达,从而影响其侵袭和转移能力。我们研究了GM-CSF对HNSCC细胞系SAS和HSC-2中MMP-2和MT1-MMP产生的影响。来自HNSCC细胞的条件培养基的明胶酶谱显示一条68 kDa的主要条带,其被鉴定为前MMP-2。GM-CSF以剂量依赖的方式刺激两种细胞系中前MMP-2的产生。与未处理的对照相比,用50 ng/ml GM-CSF处理24小时使SAS细胞中的前MMP-2活性增加3.4倍,HSC-2细胞中增加2.3倍。Northern印迹分析表明,GM-CSF导致两种细胞系中MMP-2和MT1-MMP的mRNA水平升高。结果表明GM-CSF是某些类型HNSCC中MMP-2和MT1-MMP表达的调节剂,并表明GM-CSF可能通过调节MMP-2和MT1-MMP的表达促进HNSCC的侵袭性。

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