Publication:
STAT3-Mediated Astrocyte Reactivity Associated with Brain Metastasis Contributes to Neurovascular Dysfunction.

dc.contributor.authorSarmiento Soto, Manuel
dc.contributor.authorLarkin, James R
dc.contributor.authorMartin, Chris
dc.contributor.authorKhrapitchev, Alexandre A
dc.contributor.authorMaczka, Melissa
dc.contributor.authorEconomopoulos, Vasiliki
dc.contributor.authorScott, Helen
dc.contributor.authorEscartin, Carole
dc.contributor.authorBonvento, Gilles
dc.contributor.authorSerres, Sébastien
dc.contributor.authorSibson, Nicola R
dc.date.accessioned2023-02-09T09:45:07Z
dc.date.available2023-02-09T09:45:07Z
dc.date.issued2020-10-26
dc.description.abstractAstrocytes are thought to play a pivotal role in coupling neural activity and cerebral blood flow. However, it has been shown that astrocytes undergo morphologic changes in response to brain metastasis, switching to a reactive phenotype, which has the potential to significantly compromise cerebrovascular function and contribute to the neurological sequelae associated with brain metastasis. Given that STAT3 is a key regulator of astrocyte reactivity, we aimed here to determine the impact of STAT3-mediated astrocyte reactivity on neurovascular function in brain metastasis. Rat models of brain metastasis and ciliary neurotrophic factor were used to induce astrocyte reactivity. Multimodal imaging, electrophysiology, and IHC were performed to determine the relationship between reactive astrocytes and changes in the cerebrovascular response to electrical and physiological stimuli. Subsequently, the STAT3 pathway in astrocytes was inhibited with WP1066 to determine the role of STAT3-mediated astrocyte reactivity, specifically, in brain metastasis. Astrocyte reactivity associated with brain metastases impaired cerebrovascular responses to stimuli at both the cellular and functional level and disrupted astrocyte-endothelial interactions in both animal models and human brain metastasis samples. Inhibition of STAT3-mediated astrocyte reactivity in rats with brain metastases restored cerebrovascular function, as shown by in vivo imaging, and limited cerebrovascular changes associated with tumor growth. Together these findings suggest that inhibiting STAT3-mediated astrocyte reactivity may confer significant improvements in neurological outcome for patients with brain metastases and could potentially be tested in other brain tumors. SIGNIFICANCE: These findings demonstrate that selectively targeting STAT3-mediated astrocyte reactivity ameliorates the cerebrovascular dysfunction associated with brain metastasis, providing a potential therapeutic avenue for improved patient outcome.
dc.identifier.doi10.1158/0008-5472.CAN-20-2251
dc.identifier.essn1538-7445
dc.identifier.pmid33106335
dc.identifier.unpaywallURLhttps://aacrjournals.org/cancerres/article-pdf/80/24/5642/2800767/5642.pdf
dc.identifier.urihttp://hdl.handle.net/10668/16481
dc.issue.number24
dc.journal.titleCancer research
dc.journal.titleabbreviationCancer Res
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number5642-5655
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshAnimals
dc.subject.meshAstrocytes
dc.subject.meshBrain Neoplasms
dc.subject.meshCell Line, Tumor
dc.subject.meshCerebrovascular Circulation
dc.subject.meshCiliary Neurotrophic Factor
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLaser Speckle Contrast Imaging
dc.subject.meshMagnetic Resonance Spectroscopy
dc.subject.meshMultimodal Imaging
dc.subject.meshNeoplasms, Experimental
dc.subject.meshPyridines
dc.subject.meshRats
dc.subject.meshRats, Inbred Strains
dc.subject.meshSTAT3 Transcription Factor
dc.subject.meshTyrphostins
dc.titleSTAT3-Mediated Astrocyte Reactivity Associated with Brain Metastasis Contributes to Neurovascular Dysfunction.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number80
dspace.entity.typePublication

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