dc.contributor.author
Wu, Xiaoqing
dc.contributor.author
Lu, Wenping
dc.contributor.author
Xu, Chaojie
dc.contributor.author
Jiang, Cuihong
dc.contributor.author
Zhuo, Zhili
dc.contributor.author
Wang, Ruipeng
dc.contributor.author
Zhang, Dongni
dc.contributor.author
Cui, Yongjia
dc.contributor.author
Chang, Lei
dc.contributor.author
Li, Chen
dc.date.accessioned
2023-06-05T09:15:19Z
dc.date.available
2023-06-05T09:15:19Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/39713
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-39431
dc.description.abstract
Background. The treatment of platinum-resistant recurrent ovarian cancer (PROC) is a clinical challenge and a hot topic. Tumor microenvironment (TME) as a key factor promoting ovarian cancer progression. Macrophage is a component of TME, and it has been reported that macrophage phenotype is related to the development of PROC. However, the mechanism underlying macrophage polarization and whether macrophage phenotype can be used as a prognostic indicator of PROC remains unclear. Methods. We used ESTIMATE to calculate the number of immune and stromal components in high-grade serous ovarian cancer (HGSOC) cases from The Cancer Genome Atlas database. The differential expression genes (DEGs) were analyzed via protein–protein interaction network, Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene ontology (GO) analysis to reveal major pathways of DEGs. CD80 was selected for survival analysis. IL-6 was selected for gene set enrichment analysis (GSEA). A subsequent cohort study was performed to confirm the correlation of IL-6 expression with macrophage phenotype in peripheral blood and to explore the clinical utility of macrophage phenotype for the prognosis of PROC patients. Results. A total of 993 intersecting genes were identified as candidates for further survival analysis. Further analysis revealed that CD80 expression was positively correlated with the survival of HGSOC patients. The results of GO and KEGG analysis suggested that macrophage polarization could be regulated via chemokine pathway and cytokine–cytokine receptor interaction. GSEA showed that the genes were mainly enriched in IL-6-STAT-3. Correlation analysis for the proportion of tumor infiltration macrophages revealed that M2 was correlated with IL-6. The results of a cohort study demonstrated that the regulation of macrophage phenotype by IL-6 is bidirectional. The high M1% was a protective factor for progression-free survival. Conclusion. Thus, the macrophage phenotype is a prognostic indicator in PROC patients, possibly via a hyperactive IL-6-related pathway, providing an additional clue for the therapeutic intervention of PROC.
en
dc.format.extent
15 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Macrophages Phenotype
en
dc.subject
Platinum-Resistant Serous Ovarian Cancer
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
Macrophages Phenotype Regulated by IL-6 Are Associated with the Prognosis of Platinum-Resistant Serous Ovarian Cancer: Integrated Analysis of Clinical Trial and Omics
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1155/2023/6455704
dcterms.bibliographicCitation.journaltitle
Journal of Immunology Research
dcterms.bibliographicCitation.volume
2023
dcterms.bibliographicCitation.url
https://doi.org/10.1155/2023/6455704
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2314-7156
refubium.resourceType.provider
WoS-Alert