Tumour Microenvironment-Immune Cell Interactions Influencing Breast Cancer Heterogeneity and Disease Progression
1Charles Perkins Centre, School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Breast cancer heterogeneity arises from mutations and the tumor microenvironment (TME). Targeting TME and immune-stromal interactions offers a promising therapeutic strategy for breast cancer progression and resistance.
Area of Science:
- Oncology
- Cancer Biology
- Immunology
Background:
- Breast cancer heterogeneity drives disease progression, metastasis, and therapeutic resistance.
- The tumor microenvironment (TME), comprising diverse cellular and non-cellular components, significantly influences cancer cell behavior.
- Interactions within the TME, particularly between stromal and immune cells, generate mechanical and chemical cues that impact cancer evolution.
Purpose of the Study:
- To review emerging concepts on how TME interactions contribute to breast cancer heterogeneity and progression.
- To explore the therapeutic potential of targeting the TME and its associated cellular interactions.
Main Methods:
- Literature review of current research on breast cancer heterogeneity and the TME.
- Analysis of mechanisms driving intratumoral heterogeneity.
- Discussion of therapeutic strategies targeting TME components and cell-cell communications.
Main Results:
- Germline and somatic mutations initiate heterogeneity, which is further amplified by TME-driven selective pressures.
- Stromal-immune cell interactions within the TME are critical for metastasis and can induce therapeutic resistance.
- The TME plays a crucial role in adapting cancer cells, leading to a feedback loop that enhances disease complexity.
Conclusions:
- Targeting the TME and immune-stromal cell interactions presents a viable therapeutic avenue for breast cancer.
- Understanding TME dynamics is essential for developing effective treatments against heterogeneous breast cancer.
- Therapeutic strategies focused on the TME may overcome treatment resistance and improve patient outcomes.
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