The dormant cancer cell life cycle
Tri Giang Phan1,2, Peter I Croucher3,4
1Immunology, Garvan Institute of Medical Research, Sydney, NSW, Australia. t.phan@garvan.org.au.
Abstract:
The success of targeted therapies and immunotherapies has created optimism that cancers may be curable. However, not all patients respond, drug resistance is common and many patients relapse owing to dormant cancer cells. These rare and elusive cells can disseminate early and hide in specialized niches in distant organs before being reactivated to cause disease relapse after successful treatment of the primary tumour. Despite their importance, we are yet to leverage knowledge generated from experimental models and translate the potential of targeting dormant cancer cells to prevent disease relapse in the clinic. This is due, at least in part, to the lack of adherence to consensus definitions by researchers, limited models that faithfully recapitulate this stage of metastatic spread and an absence of interdisciplinary approaches. However, the application of new high-resolution, single-cell technologies is starting to revolutionize the field and transcend classical reductionist models of studying individual cell types or genes in isolation to provide a global view of the complex underlying cellular ecosystem and transcriptional landscape that controls dormancy. In this Perspective, we synthesize some of these recent advances to describe the hallmarks of cancer cell dormancy and how the dormant cancer cell life cycle offers opportunities to target not only the cancer but also its environment to achieve a durable cure for seemingly incurable cancers.
Insights
Dormant cancer cells can cause relapse after treatment. Targeting these elusive cells and their environment offers a new strategy for durable cancer cures.
Area of Science:
- Oncology
- Cancer Biology
- Translational Medicine
Background:
- Targeted therapies and immunotherapies show promise for cancer cure, but drug resistance and relapse remain significant challenges.
- Relapse is often caused by dormant cancer cells that evade treatment and hide in specific niches.
- Current research faces hurdles due to inconsistent definitions, limited models, and lack of interdisciplinary approaches.
Purpose of the Study:
- To synthesize recent advances in understanding cancer cell dormancy.
- To describe the hallmarks of cancer cell dormancy and its life cycle.
- To identify opportunities for targeting dormant cells and their microenvironment for durable cancer cures.
Main Methods:
- Review and synthesis of recent scientific literature.
- Application of high-resolution, single-cell technologies.
- Analysis of cellular ecosystems and transcriptional landscapes controlling dormancy.
Main Results:
- Cancer cell dormancy is characterized by specific hallmarks and a distinct life cycle.
- Single-cell technologies provide a global view of the complex factors controlling dormancy.
- Dormant cancer cells can be targeted, along with their environment, to prevent relapse.
Conclusions:
- Understanding cancer cell dormancy is crucial for preventing disease relapse.
- Targeting dormant cancer cells and their niches offers a promising strategy for achieving durable cancer cures.
- Interdisciplinary approaches and advanced technologies are key to overcoming challenges in this field.
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