4.7 Review

Context-dependent roles of complement in cancer

Journal

NATURE REVIEWS CANCER
Volume 19, Issue 12, Pages 698-715

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41568-019-0210-0

Keywords

-

Categories

Funding

  1. Pierre Fabre Research Institute
  2. Association pour la Recherche sur le Cancer (ARC)
  3. Cartes d'Identite des Tumeurs (CIT) programme from the Ligue Nationale Contre le Cancer [RS19/75-111]
  4. Cancer Research for Personalized Medicine (CARPEM)
  5. Institut National du Cancer (INCa) (HTE Plan Cancer) [C1608DS]
  6. Institut National du Cancer (INCa) (PRTK G26 NIVOREN)
  7. Association pour la recherche de therapeutiques innovantes en cancerologie (ARTIC, BioniKK programme)
  8. INSERM
  9. University of Paris
  10. Sorbonne University
  11. CARPEM T8
  12. Labex Immuno-Oncology Excellence Program
  13. ARC
  14. CARPEM

Ask authors/readers for more resources

The tumour microenvironment (TME) highly influences the growth and spread of tumours, thus impacting the patient's clinical outcome. In this context, the complement system plays a major and complex role. It may either act to kill antibody-coated tumour cells, support local chronic inflammation or hamper antitumour T cell responses favouring tumour progression. Recent studies demonstrate that these opposing effects are dependent upon the sites of complement activation, the composition of the TME and the tumour cell sensitivity to complement attack. In this Review, we present the evidence that has so far accrued showing a role for complement activation and its effects on cancer control and clinical outcome under different TME contexts. We also include a new analysis of the publicly available transcriptomic data to provide an overview of the prognostic value of complement gene expression in 30 cancer types. We argue that the interplay of complement components within each cancer type is unique, governed by the properties of the tumour cells and the TME. This concept is of critical importance for the design of efficient therapeutic strategies aimed at targeting complement components and their signalling.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available