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缝隙连接蛋白 43 在中枢神经系统肿瘤侵袭和生长中的矛盾作用。

Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System.

机构信息

Laboratory of Clinical Pharmacology and Pharmacometrics, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba-shi, Chiba 263-8522, Japan.

Division of Cancer Pathophysiology, National Cancer Center Research Institute, Chuo-ku, Tokyo 104-0045, Japan.

出版信息

Int J Mol Sci. 2018 Apr 11;19(4):1159. doi: 10.3390/ijms19041159.

Abstract

The tumor microenvironment is known to have increased levels of cytokines and metabolites, such as glutamate, due to their release from the surrounding cells. A normal cell around the tumor that responds to the inflammatory environment is likely to be subsequently altered. We discuss how these abnormalities will support tumor survival via the actions of gap junctions (GJs) and hemichannels (HCs) which are composed of hexamer of connexin43 (Cx43) protein. In particular, we discuss how GJ intercellular communication (GJIC) in glioma cells, the primary brain tumor, is a regulatory factor and its attenuation leads to tumor invasion. In contrast, the astrocytes, which are normal cells around the glioma, are "hijacked" by tumor cells, either by receiving the transmission of malignant substances from the cancer cells via GJIC, or perhaps via astrocytic HC activity through the paracrine signaling which enable the delivery of these substances to the distal astrocytes. This astrocytic signaling would promote tumor expansion in the brain. In addition, brain metastasis from peripheral tissues has also been known to be facilitated by GJs formed between cerebral vascular endothelial cells and cancer cells. Astrocytes and microglia are generally thought to eliminate cancer cells at the blood-brain barrier. In contrast, some reports suggest they facilitate tumor progression as tumor cells take advantage of the normal functions of astrocytes that support the survival of the neurons by exchanging nutrients and metabolites. In summary, GJIC is essential for the normal physiological function of growth and allowing the diffusion of physiological substances. Therefore, whether GJIC is cancer promoting or suppressing may be dependent on what permeates through GJs, when it is active, and to which cells. The nature of GJs, which has been ambiguous in brain tumor progression, needs to be revisited and understood together with new findings on Cx proteins and HC activities.

摘要

肿瘤微环境由于周围细胞的释放,已知细胞因子和代谢物(如谷氨酸)水平升高。肿瘤周围对炎症环境做出反应的正常细胞很可能随后发生改变。我们讨论了这些异常如何通过间隙连接(GJ)和半通道(HC)的作用来支持肿瘤存活,这些连接由六聚体连接蛋白 43(Cx43)蛋白组成。特别是,我们讨论了脑胶质瘤(原发性脑肿瘤)细胞中的 GJ 细胞间通讯(GJIC)如何成为调节因子,其衰减会导致肿瘤侵袭。相比之下,星形胶质细胞是肿瘤周围的正常细胞,它们被肿瘤细胞“劫持”,要么通过 GJIC 从癌细胞接收恶性物质的传递,要么通过星形胶质细胞 HC 活性通过旁分泌信号传递,从而将这些物质传递给远端星形胶质细胞。这种星形胶质细胞信号会促进大脑中的肿瘤扩张。此外,已知来自周围组织的脑转移也可通过脑血内皮细胞和癌细胞之间形成的 GJ 来促进。星形胶质细胞和小胶质细胞通常被认为可以在血脑屏障处消除癌细胞。相反,一些报告表明,它们通过癌细胞利用星形胶质细胞的正常功能促进肿瘤进展,这些功能通过交换营养物质和代谢物来支持神经元的存活。总之,GJIC 对于生长的正常生理功能和生理物质的扩散是必不可少的。因此,GJIC 是否促进或抑制癌症可能取决于通过 GJ 渗透的物质、其活性以及作用的细胞。间隙连接的性质在脑肿瘤进展中一直不明确,需要结合 Cx 蛋白和 HC 活性的新发现重新审视和理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4416/5979343/57af43370618/ijms-19-01159-g001.jpg

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