Nucleic Acid Sensing in the Tumor Vasculature.

RIG-I STING TREX1 cGAS endothelial cells nucleic acid sensors tumor angiogenesis tumor microenvironment vascular inflammation vascular normalization

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
03 Sep 2021
Historique:
received: 01 07 2021
revised: 28 08 2021
accepted: 31 08 2021
entrez: 10 9 2021
pubmed: 11 9 2021
medline: 11 9 2021
Statut: epublish

Résumé

Endothelial cells form a powerful interface between tissues and immune cells. In fact, one of the underappreciated roles of endothelial cells is to orchestrate immune attention to specific sites. Tumor endothelial cells have a unique ability to dampen immune responses and thereby maintain an immunosuppressive microenvironment. Recent approaches to trigger immune responses in cancers have focused on activating nucleic acid sensors, such as cGAS-STING, in combination with immunotherapies. In this review, we present a case for targeting nucleic acid-sensing pathways within the tumor vasculature to invigorate tumor-immune responses. We introduce two specific nucleic acid sensors-the DNA sensor TREX1 and the RNA sensor RIG-I-and discuss their functional roles in the vasculature. Finally, we present perspectives on how these nucleic acid sensors in the tumor endothelium can be targeted in an antiangiogenic and immune activation context. We believe understanding the role of nucleic acid-sensing in the tumor vasculature can enhance our ability to design more effective therapies targeting the tumor microenvironment by co-opting both vascular and immune cell types.

Identifiants

pubmed: 34503262
pii: cancers13174452
doi: 10.3390/cancers13174452
pmc: PMC8431390
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL137779
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM142619
Pays : United States
Organisme : NIH HHS
ID : R01 HL137779
Pays : United States
Organisme : NIH HHS
ID : T32 GM142619-01
Pays : United States
Organisme : NIH HHS
ID : R01 HL143803
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL143803
Pays : United States

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Auteurs

Adrian M Baris (AM)

Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.

Eugenia Fraile-Bethencourt (E)

Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.

Sudarshan Anand (S)

Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR 97239, USA.
Department of Radiation Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA.

Classifications MeSH