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Intracarotid Cancer Cell Injection to Produce Mouse Models of Brain Metastasis
Published on: February 8, 2017
Hormonal and neuronal interactions shaping the brain metastatic microenvironment
Stephen Shovlin1, Leonie S Young2, Damir Varešlija3
1School of Pharmacy and Biomolecular Sciences, RCSI University of Medicine and Health Sciences, Dublin, Ireland.
Abstract:
Metastatic progression drives the majority of cancer-related fatalities, and involvement of the central nervous system (CNS) poses especially formidable challenges to patients and clinicians. Brain metastases (BrM), commonly originate from lung, breast and melanoma cancers, and carry disproportionately poor outcomes. Although therapeutic advances have extended survival for many extracranial tumors, BrM incidence continues to climb-underscoring critical knowledge gaps in understanding the unique biology of tumor colonization in the CNS. While definitive evidence remains limited, a growing focus on cancer neuroscience-especially regarding hormone dependent cancer cells in the brain-has begun to reveal that factors normally regulated by sex steroids and neurosteroids may similarly influence the specialized metastatic microenvironment in the CNS. Steroid hormones can permeate the blood-brain barrier (BBB) or be synthesized de novo by astrocytes and other CNS-resident cells, potentially influencing processes such as inflammation, synaptic plasticity, and immune surveillance. However, how these hormonal pathways are co-opted by disseminated cancer cells remains unclear. Here, we review the complex hormonal landscape of the adult brain and examine how neuroendocrine-immune interactions, often regulated by sex hormones, may support metastatic growth. We discuss the interplay between systemic hormones, local steroidogenesis, and tumor adaptation to identify novel therapeutic opportunities.
Insights
Brain metastases (BrM) are a major challenge in cancer. This review explores how hormones and neuroendocrine-immune interactions in the brain may fuel BrM growth, suggesting new therapeutic targets.
Area of Science:
- Neuroscience
- Oncology
- Endocrinology
Background:
- Metastatic progression, particularly to the central nervous system (CNS), is a leading cause of cancer mortality.
- Brain metastases (BrM) from lung, breast, and melanoma cancers have poor prognoses, despite advances in treating extracranial tumors.
- The increasing incidence of BrM highlights gaps in understanding CNS tumor biology and colonization.
Purpose of the Study:
- To review the hormonal landscape of the adult brain in the context of cancer neuroscience.
- To examine how neuroendocrine-immune interactions, influenced by sex hormones, may promote metastatic growth within the CNS.
- To identify novel therapeutic opportunities by understanding the interplay between hormones and tumor adaptation.
Main Methods:
- Literature review of existing research on brain metastases, cancer neuroscience, and hormonal regulation in the CNS.
- Analysis of the role of sex steroids and neurosteroids in the brain microenvironment.
- Exploration of neuroendocrine-immune interactions and their influence on tumor growth.
Main Results:
- Steroid hormones can cross the blood-brain barrier or be synthesized within the CNS, affecting inflammation, synaptic plasticity, and immune surveillance.
- Hormonal pathways normally involved in brain function may be co-opted by cancer cells to support colonization and growth.
- The interplay between systemic hormones, local steroidogenesis, and tumor adaptation is crucial for BrM development.
Conclusions:
- Understanding the brain's hormonal milieu is critical for addressing the challenges of brain metastases.
- Neuroendocrine-immune pathways represent promising targets for novel therapeutic strategies against BrM.
- Further research into hormone-tumor interactions in the CNS can lead to improved patient outcomes.
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