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IL-12 和 IL-27 驱动的人肿瘤血管生成趋化因子的调节。

Regulation of angiostatic chemokines driven by IL-12 and IL-27 in human tumors.

机构信息

Department of Experimental and Laboratory Medicine, G. Gaslini Institute, Genova, Italy.

出版信息

J Leukoc Biol. 2011 Nov;90(5):875-82. doi: 10.1189/jlb.0511237. Epub 2011 Jul 12.

Abstract

Chemokines have pleiotropic effects in regulating immunity, angiogenesis, and tumor growth. CXC and CC chemokine families members and their receptors are able to exert a proangiogenic or an antiangiogenic effect in experimental models and in human tumors. In this review article, we have summarized literature data and our studies concerning the angiostatic activity of chemokines. Their angiostatic activity may be a result of a direct effect on the biological functions of endothelial cells and/or an effect on tumor cells inhibiting their capability to stimulate new blood vessel formation. Moreover, chemokines have a pro- and antitumor effect within the tumor microenvironment by regulating immune cell infiltration and its antitumor activities. We have focused our interest on the role of IL-12 and IL-27 in solid and hematological tumors, and we have suggested and discussed their potential use as antiangiogenic agents in the treatment of such tumors.

摘要

趋化因子在调节免疫、血管生成和肿瘤生长方面具有多效性。CXC 和 CC 趋化因子家族成员及其受体能够在实验模型和人类肿瘤中发挥促血管生成或抗血管生成作用。在这篇综述文章中,我们总结了有关趋化因子血管抑制活性的文献数据和我们的研究。它们的血管抑制活性可能是直接作用于内皮细胞的生物学功能的结果,或者是通过抑制肿瘤细胞刺激新血管形成的能力而产生的作用。此外,趋化因子通过调节免疫细胞浸润及其抗肿瘤活性在肿瘤微环境中具有促肿瘤和抗肿瘤作用。我们关注了白细胞介素-12 和白细胞介素-27 在实体瘤和血液系统肿瘤中的作用,并提出并讨论了它们作为此类肿瘤抗血管生成治疗剂的潜在用途。

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