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白细胞介素-27对黑色素瘤的抗肿瘤活性。

Antitumor activities of interleukin-27 on melanoma.

作者信息

Nagai Hiroshi, Oniki Shuntaro, Fujiwara Susumu, Xu Mingli, Mizoguchi Izuru, Yoshimoto Takayuki, Nishigori Chikako

机构信息

Department of Internal Related, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Endocr Metab Immune Disord Drug Targets. 2010 Mar;10(1):41-6. doi: 10.2174/187153010790827920.

Abstract

The worldwide incidence of malignant melanoma has been steadily increasing, and it has become a major public health problem in many countries. Melanoma has been considered as a prototypical "immunogenic" tumor on the basis of clinical observations showing that primary lesions can spontaneously regress and that immunosuppressed individuals have an increased incidence of melanoma. Thus, various immunological therapies have been intensively conducted for the treatment of melanoma. Interleukin(IL)-27 is a IL-12-related heterodimeric cytokine composed of p28 and EBV-induced gene 3 subunits that are structurally related to the p35 and p40 subunits of IL-12, respectively. Recent studies reveal that IL-27 exhibits not only potent antitumor immune activities via cytotoxic T lymphocytes or natural killer cells but also an antiangiogenic effect. We recently clarified that IL-27 possesses an antiproliferative activity on melanoma cells. This review summarizes anti-tumor responses induced by IL-27 and novel anti-melanoma activities of IL-27.

摘要

恶性黑色素瘤的全球发病率一直在稳步上升,并且在许多国家已成为一个主要的公共卫生问题。基于临床观察,即原发性病变可自发消退以及免疫抑制个体患黑色素瘤的发病率增加,黑色素瘤被认为是一种典型的“免疫原性”肿瘤。因此,已经针对黑色素瘤的治疗广泛开展了各种免疫疗法。白细胞介素(IL)-27是一种与IL-12相关的异二聚体细胞因子,由p28和EB病毒诱导基因3亚基组成,它们在结构上分别与IL-12的p35和p40亚基相关。最近的研究表明,IL-27不仅通过细胞毒性T淋巴细胞或自然杀伤细胞表现出强大的抗肿瘤免疫活性,而且还具有抗血管生成作用。我们最近阐明,IL-27对黑色素瘤细胞具有抗增殖活性。本综述总结了IL-27诱导的抗肿瘤反应以及IL-27的新型抗黑色素瘤活性。

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