Vascular-Associated Mononuclear Phagocytes: First-Line Soldiers Ambushing Metastasis.
Han-Ying Huang1, Xin-Nan Zheng1, Lin Tian1
1State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, P. R. China.
Summary
Vascular-associated mononuclear phagocytes (VaMPs) patrol blood vessels, identifying and fighting early-stage cancer spread. Understanding their plasticity and targeting them offers new metastasis treatment strategies.
Area of Science:
- Immunology
- Cell Biology
- Oncology
Background:
- Mononuclear phagocytes (MPs) maintain tissue homeostasis by eliminating abnormal cells.
- Vascular-associated mononuclear phagocytes (VaMPs) are crucial sentinels against disseminated tumor cells.
- VaMPs exhibit diverse lifespans and phenotypes influenced by their microenvironment.
Purpose of the Study:
- To review the roles of patrolling monocytes, Kupffer cells, and perivascular macrophages in immunosurveillance during incipient metastasis.
- To explore the molecular mechanisms, including transcription factors and cell surface receptors, underlying VaMP anti-tumor activity.
- To summarize strategies for targeting VaMPs in overt metastasis.
Main Methods:
- Literature review of existing research on mononuclear phagocytes and metastasis.
- Analysis of molecular and cellular mechanisms driving VaMP phenotypic plasticity.
- Synthesis of current knowledge on VaMP roles in immunosurveillance.
Main Results:
- Identified three key VaMP types: patrolling monocytes, Kupffer cells, and perivascular macrophages.
- Highlighted the importance of lineage-determining transcription factors and cell surface receptors in VaMP anti-tumor functions.
- Discussed the phenotypic plasticity of VaMPs in response to the microenvironment.
Conclusions:
- VaMPs play a critical role in immunosurveillance against early-stage cancer metastasis.
- Targeting VaMPs presents a promising therapeutic strategy for managing overt metastasis.
- Further research into VaMP plasticity can optimize anti-cancer treatments.
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