dc.contributor.author
Bose, Debojit
dc.date.accessioned
2018-06-08T10:41:00Z
dc.date.available
2018-06-01T10:12:57.699Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20881
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-24180
dc.description.abstract
The last two decades have witnessed enormous growth in the field of cancer
immunity. Mechanistic insights of cancer immunoediting have not only enhanced
our understanding but also paved the way to target and/or harness the innate
immune system to combat cancer, called cancer immunotherapy. Cyclic GMP-AMP
synthase (cGAS)/Stimulator of interferon genes(STING) pathway has recently
emerged as nodal player in cancer immunity and is currently being explored as
potential therapeutic target. Although therapeutic activation of this pathway
has shown promising anti-tumor effects in vivo, evidence also indicates the
role of this pathway in inflammation mediated carcinogenesis. This review
highlights our current understanding of cGAS/STING pathway in cancer, its
therapeutic targeting and potential alternate approaches to target this
pathway. Optimal therapeutic targeting and artificial tunability of this
pathway still demand in depth understanding of cGAS/STING pathway regulation
and homeostasis. View Full-Text
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Cyclic guanosine monophosphate–adenosine monophosphate (cGAMP)
dc.subject
cancer immunotherapy
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie
dc.title
cGAS/STING Pathway in Cancer
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Int. J. Mol. Sci. - 18 (2017), 11, Artikel Nr. 2456
dc.title.subtitle
Jekyll and Hyde Story of Cancer Immune Response
dcterms.bibliographicCitation.doi
10.3390/ijms18112456
dcterms.bibliographicCitation.url
http://doi.org/10.3390/ijms18112456
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000029843
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000009788
dcterms.accessRights.openaire
open access