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Tumor-Associated Macrophages: From Mechanisms to Therapy

期刊

IMMUNITY
卷 41, 期 1, 页码 49-61

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2014.06.010

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资金

  1. NIH [RO1 CA172451, PO1 CA100324]
  2. Rowley Breast Cancer Scientific Research Project [1003251030]
  3. Wellcome Trust, UK
  4. Wellcome Trust [101067/Z/13/Z] Funding Source: Wellcome Trust
  5. MRC [G1002033] Funding Source: UKRI
  6. Medical Research Council [G1002033] Funding Source: researchfish
  7. Wellcome Trust [101067/Z/13/Z] Funding Source: researchfish

向作者/读者索取更多资源

The tumor microenvironment is a complex ecology of cells that evolves with and provides support to tumor cells during the transition to malignancy. Among the innate and adaptive immune cells recruited to the tumor site, macrophages are particularly abundant and are present at all stages of tumor progression. Clinical studies and experimental mouse models indicate that these macrophages generally play a protumoral role. In the primary tumor, macrophages can stimulate angiogenesis and enhance tumor cell invasion, motility, and intravasation. During monocytes and/or metastasis, macrophages prime the premetastatic site and promote tumor cell extravasation, survival, and persistent growth. Macrophages are also immunosuppressive, preventing tumor cell attack by natural killer and T cells during tumor progression and after recovery from chemo-or immunotherapy. Therapeutic success in targeting these protumoral roles in preclinical models and in early clinical trials suggests that macrophages are attractive targets as part of combination therapy in cancer treatment.

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