Related Experiment Video
Updated: Mar 8, 2026

07:43
Intracarotid Cancer Cell Injection to Produce Mouse Models of Brain Metastasis
Published on: February 8, 2017
28.3K
Breast Cancer Brain Metastases: Clonal Evolution in Clinical Context
Jodi M Saunus1,2, Amy E McCart Reed3,4, Zhun Leong Lim5,6
1The University of Queensland (UQ), UQ Centre for Clinical Research, Herston, Queensland 4029, Australia. j.saunus@uq.edu.au.
International Journal of Molecular Sciences
|January 19, 2017
Summary
Brain metastases, often resistant to therapies due to the blood-brain barrier, adapt within the brain niche. Understanding their genomic landscape and the neural environment is key to improving treatment for this growing breast cancer challenge.
Area of Science:
- Oncology
- Neuroscience
- Genomics
Background:
- Brain metastases represent a significant challenge in breast cancer, with rising incidence.
- The blood-brain barrier (BBB) has historically limited therapeutic efficacy.
- Emerging evidence suggests dynamic tumor evolution and increased permeability within the brain.
Purpose of the Study:
- To review experimental approaches and studies on the genomic landscape of breast cancer brain metastases.
- To contextualize clonal outgrowth factors, including tumor cell capabilities and the neural niche.
- To discuss factors contributing to treatment resistance and outline current clinical trials.
Main Methods:
- Review of experimental approaches.
- Analysis of landmark studies on genomic landscape.
- Contextualization with factors impacting clonal outgrowth and clinical behavior.
Main Results:
- Breast cancer brain metastases exhibit exceptional adaptability within the unique brain microenvironment.
- The brain can transition from a sanctuary to a tumor-supportive niche.
- Genomic profiling reveals insights into tumor evolution and adaptation.
Conclusions:
- Understanding the genomic landscape and brain microenvironment is crucial for managing breast cancer brain metastases.
- Factors like late detection and altered vascular dynamics contribute to treatment resistance.
- Precision management and ongoing clinical trials offer hope for improved outcomes.
Related Concept Videos
Tumor Progression
7.7K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
7.7K
Metastasis
6.7K
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
6.7K
T Cell Activation and Clonal Selection
16.9K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
16.9K

