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在骨肉瘤细胞系中补体系统的激活通过增强生长因子的产生促进血管生成。

Activation of the complement system in an osteosarcoma cell line promotes angiogenesis through enhanced production of growth factors.

机构信息

Department of Microbiology and Immunology, Eulji University School of Medicine, Daejeon, 34824, South Korea.

Eulji Biomedical Science Research Institute, Eulji University School of Medicine, Daejeon, 34824, Republic of Korea.

出版信息

Sci Rep. 2018 Apr 3;8(1):5415. doi: 10.1038/s41598-018-23851-z.

Abstract

There is increasing evidence that the complement system is activated in various cancer tissues. Besides being involved in innate immunity against pathogens, the complement system also participates in inflammation and the modulation of tumor microenvironment. Recent studies suggest that complement activation promotes tumor progression in various ways. Among some cancer cell lines, we found that human bone osteosarcoma epithelial cells (U2-OS) can activate the alternative pathway of the complement system by pooled normal human serum. Interestingly, U2-OS cells showed less expression of complement regulatory proteins, compared to other cancer cell lines. Furthermore, the activated complement system enhanced the production of growth factors, which promoted angiogenesis of human endothelial cells. Our results demonstrated a direct linkage between the complement system and angiogenesis using the in vitro model, which suggest the complement system and related mechanisms might be potential targets for cancer treatment.

摘要

越来越多的证据表明,补体系统在各种癌症组织中被激活。补体系统除了参与针对病原体的先天免疫外,还参与炎症和肿瘤微环境的调节。最近的研究表明,补体的激活以多种方式促进肿瘤的进展。在一些癌细胞系中,我们发现人骨肉瘤上皮细胞(U2-OS)可以通过混合正常人血清激活补体系统的替代途径。有趣的是,与其他癌细胞系相比,U2-OS 细胞表达的补体调节蛋白较少。此外,激活的补体系统增强了生长因子的产生,从而促进了人内皮细胞的血管生成。我们的研究结果通过体外模型证明了补体系统与血管生成之间的直接联系,这表明补体系统和相关机制可能是癌症治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b567/5883033/0902de327e13/41598_2018_23851_Fig1_HTML.jpg

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