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再生增强转移:神经血管信号在促进黑色素瘤脑转移中的新作用。

Regeneration Enhances Metastasis: A Novel Role for Neurovascular Signaling in Promoting Melanoma Brain Metastasis.

作者信息

Prakash Roshini, Izraely Sivan, Thareja Nikita S, Lee Rex H, Rappaport Maya, Kawaguchi Riki, Sagi-Assif Orit, Ben-Menachem Shlomit, Meshel Tsipi, Machnicki Michal, Ohe Shuichi, Hoon Dave S, Coppola Giovanni, Witz Isaac P, Carmichael S Thomas

机构信息

Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.

Department of Cell Research and Immunology, School of Molecular Cell Biology and Biotechnology, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.

出版信息

Front Neurosci. 2019 Apr 9;13:297. doi: 10.3389/fnins.2019.00297. eCollection 2019.

Abstract

Neural repair after stroke involves initiation of a cellular proliferative program in the form of angiogenesis, neurogenesis, and molecular growth signals in the surrounding tissue elements. This cellular environment constitutes a niche in which regeneration of new blood vessels and new neurons leads to partial tissue repair after stroke. Cancer metastasis has similar proliferative cellular events in the brain and other organs. Do cancer and CNS tissue repair share similar cellular processes? In this study, we identify a novel role of the regenerative neurovascular niche induced by stroke in promoting brain melanoma metastasis through enhancing cellular interactions with surrounding niche components. Repair-mediated neurovascular signaling induces metastatic cells to express genes crucial to metastasis. Mimicking stroke-like conditions displays an enhancement of metastatic migration potential and allows for the determination of cell-specific signals produced by the regenerative neurovascular niche. Comparative analysis of both and expression profiles reveals a major contribution of endothelial cells in mediating melanoma metastasis. These results point to a previously undiscovered role of the regenerative neurovascular niche in shaping the tumor microenvironment and brain metastatic landscape.

摘要

中风后的神经修复涉及以血管生成、神经发生以及周围组织成分中的分子生长信号等形式启动细胞增殖程序。这种细胞环境构成了一个微环境,其中新血管和新神经元的再生导致中风后部分组织修复。癌症转移在大脑和其他器官中具有类似的增殖性细胞事件。癌症与中枢神经系统组织修复是否共享相似的细胞过程?在本研究中,我们确定了中风诱导的再生神经血管微环境在通过增强与周围微环境成分的细胞相互作用促进脑黑色素瘤转移方面的新作用。修复介导的神经血管信号传导诱导转移细胞表达对转移至关重要的基因。模拟中风样条件显示转移迁移潜力增强,并有助于确定再生神经血管微环境产生的细胞特异性信号。对两者表达谱的比较分析揭示了内皮细胞在介导黑色素瘤转移中的主要作用。这些结果表明再生神经血管微环境在塑造肿瘤微环境和脑转移格局方面具有先前未被发现的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5935/6465799/2100471cac57/fnins-13-00297-g001.jpg

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