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Immune microenvironments in solid tumors: new targets for therapy

期刊

GENES & DEVELOPMENT
卷 25, 期 24, 页码 2559-2572

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.169029.111

关键词

leukocyte; inflammation; chemotherapy; radiation therapy; cytotoxic therapy; cancer

资金

  1. American Board of Radiology (ABR)
  2. Conquer Cancer Foundation of the American Society for Clinical Oncology (ASCO)
  3. Cancer Research UK
  4. Breast Cancer Research Foundation
  5. NIH/NCI
  6. Department of Defense [W81XWH-11-1-0702, PR080717]
  7. Susan G. Komen for the Cure Foundation [KG111084]

向作者/读者索取更多资源

Leukocytes and their soluble mediators play important regulatory roles in all aspects of solid tumor development. While immunotherapeutic strategies have conceptually held clinical promise, with the exception of a small percentage of patients, they have failed to demonstrate effective, consistent, and durable anti-cancer responses. Several subtypes of leukocytes that commonly infiltrate solid tumors harbor immunosuppressive activity and undoubtedly restrict the effectiveness of these strategies. Several of these same immune cells also foster tumor development by expression of potent protumor mediators. Given recent evidence revealing that immune-based mechanisms regulate the response to conventional cytotoxic therapy, it seems reasonable to speculate that tumor progression could be effectively diminished by combining cytotoxic strategies with therapies that blunt protumor immune-based effectors and/or neutralize those that instead impede development of desired anti-tumor immunity, thus providing synergistic effects between traditional cytotoxic and immune-modulatory approaches.

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