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Updated: Feb 5, 2026

Enrichment and Characterization of the Tumor Immune and Non-immune Microenvironments in Established Subcutaneous Murine Tumors
Published on: June 7, 2018
Efferocytosis in the tumor microenvironment
Thomas A Werfel1, Rebecca S Cook2,3,4,5
1Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, 759 Preston Research Building, 2220 Pierce Ave, Nashville, TN, 37232, USA.
Programmed cell death, or apoptosis, is managed by efferocytosis, a process where phagocytes clear apoptotic cells to prevent inflammation and maintain tissue homeostasis. Dysfunctional efferocytosis contributes to disease and cancer immunosuppression.
Area of Science:
- Immunology
- Cell Biology
- Pathology
Background:
- Millions of human cells undergo programmed cell death (apoptosis) every minute.
- Apoptotic cells risk secondary necrosis, releasing inflammatory intracellular contents.
- Efferocytosis, the engulfment of apoptotic cells by phagocytes, prevents inflammation and maintains tissue homeostasis.
Purpose of the Study:
- To explore the molecular mechanisms of efferocytosis.
- To understand how efferocytosis failure contributes to disease.
- To investigate cancer's exploitation of efferocytosis for immune evasion.
Main Methods:
- Review of current literature on efferocytosis.
- Analysis of molecular pathways involved in efferent recognition and engulfment.
- Examination of the role of efferocytosis in tumor microenvironments.
Main Results:
- Efferocytosis is crucial for preventing inflammation and maintaining tissue homeostasis during normal cell turnover.
- Failures in efferocytosis are linked to various diseases.
- Cancers leverage efferocytosis to create an immunosuppressive tumor microenvironment, promoting tumor growth and immune evasion.
Conclusions:
- Efferocytosis is a vital physiological process with significant implications in disease pathogenesis.
- Targeting efferocytosis presents a potential therapeutic strategy, particularly as an adjunct to cancer treatments.
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