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Targeting Tumor Associated Macrophages to Overcome Conventional Treatment Resistance in Glioblastoma

期刊

FRONTIERS IN PHARMACOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2020.00368

关键词

glioblastoma; macrophages; microglia; resistance; radiation; crosstalks; tumor-associated macrophage

资金

  1. French national research agency (ANR) through the LabEx IRON Innovative Radiopharmaceuticals in Oncology and Neurology as part of the French government Investissements d'Avenir program [ANR-11-LABX-0018]
  2. ANR
  3. University of Angers (Angers, France)
  4. La Region Pays-de-la-Loire
  5. Canceropole Grand-Ouest (Vectorization, imaging and radiotherapies network)
  6. LabEX IGO through the investment of the future program [ANR-11-LABX0016-01]
  7. ANR through the investment of the future program [ANR-11-LABX0016-01]
  8. INCa
  9. Ministry of Health and the Institute for Health and Medical Research (Inserm) [INCa-DGOS-Inserm_12558]
  10. LabEx IRON
  11. LabEx IRON-2
  12. University of Angers
  13. Institut National de la Sante et de la RechercheMedicale (INSERM)

向作者/读者索取更多资源

Glioblastoma (GB) is the most common and devastating form of brain cancer. Despite conventional treatments, progression or recurrences are systematic. In recent years, immunotherapies have emerged as an effective treatment in a number of cancers, leaving the question of their usefulness also faced with the particular case of brain tumors. The challenge here is major not only because the brain is the seat of our consciousness but also because of its isolation by the blood-brain barrier and the presence of a unique microenvironment that constitutes the central nervous system (CNS) with very specific constituent or patrolling cells. Much of the microenvironment is made up of immune cells or inflammation. Among these, tumor-associated macrophages (TAMs) are of significant interest as they are often involved in facilitating tumor progression as well as the development of resistance to standard therapies. In this review, the ubiquity of TAMs in GB will be discussed while the specific case of microglia resident in the brain will be also emphasized. In addition, the roles of TAMs as accomplices in the progression of GB and resistance to treatment will be presented. Finally, clinical trials targeting TAMs as a means of treating cancer will be discussed.

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