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抗白细胞介素-6 受体抗体抑制人结肠癌细胞的进展。

Anti-interleukin-6 receptor antibody inhibits the progression in human colon carcinoma cells.

机构信息

Department of Medical Laboratory Science and Biotechnology, Yuanpei University, Hsin-Chu City, Taiwan.

出版信息

Eur J Clin Invest. 2011 Mar;41(3):277-84. doi: 10.1111/j.1365-2362.2010.02405.x. Epub 2010 Nov 26.

DOI:10.1111/j.1365-2362.2010.02405.x
PMID:21114487
Abstract

BACKGROUND

Interleukin-6 (IL-6) promotes proliferation and invasion in colorectal carcinoma, and serum IL-6 levels are correlated with survival in patients with colorectal carcinoma. In this study, we attempted to clarify the signal pathway downstream of IL-6 and the role of the IL-6 receptor complex in terms of the biological effects of clonogenic growth and invasiveness in colorectal carcinoma cells.

MATERIALS AND METHODS

IL-6-stimulated SW480 cells were treated with IL-6 receptor neutralization antibody, mitogen-activated protein kinase (MAPK) inhibitor and phosphatidylinositol 3-kinase inhibitor, and clonogenic growth and invasiveness were assessed. IL-6 and IL-6 receptor-expressing LoVo cells were also tested the IL-6 receptor antibody effect. The downstream molecules of the IL-6-mediated pathway were also evaluated.

RESULTS

IL-6 effectively enhanced the clonogenicity and invasiveness of SW480; however, these abilities were reversed by treatment with anti-IL-6 receptor antibody, and MAPK and PI3K inhibitors exhibited partial ability to reduce these effects. Similar effects were also found in anti-IL-6 receptor antibody-treated LoVo cells in addition of modulating STAT3 pathway. Anti-IL-6 receptor antibody also inhibited matrix metalloproteinase-2 (MMP-2) and 9 (MMP-9) expressions in IL-6-stimulated SW480.

CONCLUSIONS

IL-6 and the IL-6R complex could induce clonogenic growth and invasiveness by mediating signals in the Ras/MAPK and PI3K/AKt pathways, and the malignant phenotypes might be associated with the production of MMP-2 and MMP-9 after IL-6 stimulation in SW480 cancer cells.

摘要

背景

白细胞介素-6(IL-6)促进结直肠癌的增殖和侵袭,血清 IL-6 水平与结直肠癌患者的生存相关。在这项研究中,我们试图阐明 IL-6 下游的信号通路以及 IL-6 受体复合物在结直肠癌细胞的集落生长和侵袭性生物学效应中的作用。

材料和方法

用 IL-6 受体中和抗体、丝裂原活化蛋白激酶(MAPK)抑制剂和磷酸肌醇 3-激酶抑制剂处理 IL-6 刺激的 SW480 细胞,评估集落生长和侵袭性。还测试了表达 IL-6 和 IL-6 受体的 LoVo 细胞的 IL-6 受体抗体作用。还评估了 IL-6 介导途径的下游分子。

结果

IL-6 有效增强了 SW480 的集落形成能力和侵袭性;然而,这些能力被抗 IL-6 受体抗体的治疗逆转,MAPK 和 PI3K 抑制剂表现出部分降低这些效应的能力。在抗 IL-6 受体抗体处理的 LoVo 细胞中也发现了类似的效果,除了调节 STAT3 途径之外。抗 IL-6 受体抗体还抑制了 IL-6 刺激的 SW480 中基质金属蛋白酶-2(MMP-2)和 9(MMP-9)的表达。

结论

IL-6 和 IL-6R 复合物可以通过介导 Ras/MAPK 和 PI3K/AKt 通路中的信号诱导集落生长和侵袭性,并且恶性表型可能与 IL-6 刺激后 SW480 癌细胞中 MMP-2 和 MMP-9 的产生有关。

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