Suppr超能文献

敌友?神经血管单元在脑转移形成中的双面性。

Foe or friend? Janus-faces of the neurovascular unit in the formation of brain metastases.

机构信息

1 Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.

2 Institute of Life Sciences, Vasile Goldiş Western University of Arad, Arad, Romania.

出版信息

J Cereb Blood Flow Metab. 2018 Apr;38(4):563-587. doi: 10.1177/0271678X17732025. Epub 2017 Sep 18.

Abstract

Despite the potential obstacle represented by the blood-brain barrier for extravasating malignant cells, metastases are more frequent than primary tumors in the central nervous system. Not only tightly interconnected endothelial cells can hinder metastasis formation, other cells of the brain microenvironment (like astrocytes and microglia) can also be very hostile, destroying the large majority of metastatic cells. However, malignant cells that are able to overcome these harmful mechanisms may benefit from the shielding and even support provided by cerebral endothelial cells, astrocytes and microglia, rendering the brain a sanctuary site against anti-tumor strategies. Thus, cells of the neurovascular unit have a Janus-faced attitude towards brain metastatic cells, being both destructive and protective. In this review, we present the main mechanisms of brain metastasis formation, including those involved in extravasation through the brain vasculature and survival in the cerebral environment.

摘要

尽管血脑屏障对恶性细胞渗出构成了潜在的障碍,但转移瘤在中枢神经系统中的发生率高于原发性肿瘤。不仅紧密相互连接的内皮细胞可以阻碍转移形成,脑微环境中的其他细胞(如星形胶质细胞和小胶质细胞)也可能非常具有敌意,破坏绝大多数转移性细胞。然而,能够克服这些有害机制的恶性细胞可能会受益于大脑内皮细胞、星形胶质细胞和小胶质细胞提供的屏蔽甚至支持,使大脑成为对抗抗肿瘤策略的避难所。因此,神经血管单元的细胞对脑转移细胞具有两面性,既具有破坏性又具有保护性。在这篇综述中,我们介绍了脑转移形成的主要机制,包括通过脑血管渗透和在脑环境中存活的机制。

相似文献

1
Foe or friend? Janus-faces of the neurovascular unit in the formation of brain metastases.
J Cereb Blood Flow Metab. 2018 Apr;38(4):563-587. doi: 10.1177/0271678X17732025. Epub 2017 Sep 18.
2
Response of the neurovascular unit to brain metastatic breast cancer cells.
Acta Neuropathol Commun. 2019 Aug 19;7(1):133. doi: 10.1186/s40478-019-0788-1.
3
STAT3-Mediated Astrocyte Reactivity Associated with Brain Metastasis Contributes to Neurovascular Dysfunction.
Cancer Res. 2020 Dec 15;80(24):5642-5655. doi: 10.1158/0008-5472.CAN-20-2251. Epub 2020 Oct 26.
5
Cells of the Blood-Brain Barrier: An Overview of the Neurovascular Unit in Health and Disease.
Methods Mol Biol. 2022;2492:3-24. doi: 10.1007/978-1-0716-2289-6_1.
6
Characterization of the blood-brain barrier of metastatic and primary malignant neoplasms.
J Neurosurg. 2013 Aug;119(2):427-33. doi: 10.3171/2013.3.JNS122226. Epub 2013 Apr 26.
7
Glioma-induced remodeling of the neurovascular unit.
Brain Res. 2009 Sep 8;1288:125-34. doi: 10.1016/j.brainres.2009.06.095. Epub 2009 Jul 9.
8
Brain mesenchymal stem cells: physiology and pathological implications.
Dev Growth Differ. 2016 Jun;58(5):469-80. doi: 10.1111/dgd.12296. Epub 2016 Jun 7.
9
Role of the neurovascular unit in the process of cerebral ischemic injury.
Pharmacol Res. 2020 Oct;160:105103. doi: 10.1016/j.phrs.2020.105103. Epub 2020 Jul 31.

引用本文的文献

1
Inflammasome activation in peritumoral astrocytes is a key player in breast cancer brain metastasis development.
Acta Neuropathol Commun. 2023 Sep 25;11(1):155. doi: 10.1186/s40478-023-01646-2.
2
The Role of Microglia in Brain Metastases: Mechanisms and Strategies.
Aging Dis. 2024 Feb 1;15(1):169-185. doi: 10.14336/AD.2023.0514.
7
Drug delivery for neuronopathic lysosomal storage diseases: evolving roles of the blood brain barrier and cerebrospinal fluid.
Metab Brain Dis. 2022 Aug;37(6):1745-1756. doi: 10.1007/s11011-021-00893-3. Epub 2022 Jan 28.
8
Microphysiological systems to study tumor-stroma interactions in brain cancer.
Brain Res Bull. 2021 Sep;174:220-229. doi: 10.1016/j.brainresbull.2021.06.012. Epub 2021 Jun 21.
9
10
Site-specific metastasis: A cooperation between cancer cells and the metastatic microenvironment.
Int J Cancer. 2021 Mar 15;148(6):1308-1322. doi: 10.1002/ijc.33247. Epub 2020 Aug 27.

本文引用的文献

1
Malignant pericytes expressing GT198 give rise to tumor cells through angiogenesis.
Oncotarget. 2017 May 25;8(31):51591-51607. doi: 10.18632/oncotarget.18196. eCollection 2017 Aug 1.
2
Emerging strategies for delivering antiangiogenic therapies to primary and metastatic brain tumors.
Adv Drug Deliv Rev. 2017 Sep 15;119:159-174. doi: 10.1016/j.addr.2017.06.011. Epub 2017 Jun 22.
3
Cooperation of neurotrophin receptor TrkB and Her2 in breast cancer cells facilitates brain metastases.
Breast Cancer Res. 2017 Apr 26;19(1):51. doi: 10.1186/s13058-017-0844-3.
4
CCR4 is a determinant of melanoma brain metastasis.
Oncotarget. 2017 May 9;8(19):31079-31091. doi: 10.18632/oncotarget.16076.
5
The roles of microglia/macrophages in tumor progression of brain cancer and metastatic disease.
Front Biosci (Landmark Ed). 2017 Jun 1;22(10):1805-1829. doi: 10.2741/4573.
7
Brain metastasization of breast cancer.
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):132-147. doi: 10.1016/j.bbcan.2017.03.004. Epub 2017 Mar 21.
8
Targeted Treatment of Brain Metastases.
Curr Neurol Neurosci Rep. 2017 Apr;17(4):37. doi: 10.1007/s11910-017-0741-2.
9
Astrocyte-induced Reelin expression drives proliferation of Her2 breast cancer metastases.
Clin Exp Metastasis. 2017 Feb;34(2):185-196. doi: 10.1007/s10585-017-9839-9. Epub 2017 Feb 17.
10
Breast Cancer Brain Metastases: Clonal Evolution in Clinical Context.
Int J Mol Sci. 2017 Jan 13;18(1):152. doi: 10.3390/ijms18010152.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验