Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28641
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dc.contributor.authorTo, Sarah Q-
dc.contributor.authorDmello, Rhynelle S-
dc.contributor.authorRichards, Anna K-
dc.contributor.authorErnst, Matthias-
dc.contributor.authorChand, Ashwini L-
dc.date2022-
dc.date.accessioned2022-01-28T05:11:26Z-
dc.date.available2022-01-28T05:11:26Z-
dc.date.issued2022-01-15-
dc.identifier.citationCancers 2022; 14(2): 429.en
dc.identifier.issn2072-6694
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28641-
dc.description.abstractInterleukin (IL)-6 family cytokines, such as IL-6 and IL-11, are defined by the shared use of the gp130 receptor for the downstream activation of STAT3 signaling and the activation of genes which contribute to the "hallmarks of cancer", including proliferation, survival, invasion and metastasis. Increased expression of these cytokines, or the ligand-specific receptors IL-6R and IL-11RA, in breast tumors positively correlate to disease progression and poorer patient outcome. In this review, we examine evidence from pre-clinical studies that correlate enhanced IL-6 and IL-11 mediated gp130/STAT3 signaling to the progression of breast cancer. Key processes by which the IL-6 family cytokines contribute to the heterogeneous nature of breast cancer, immune evasion and metastatic potential, are discussed. We examine the latest research into the therapeutic targeting of IL-6 family cytokines that inhibit STAT3 transcriptional activity as a potential breast cancer treatment, including current clinical trials. The importance of the IL-6 family of cytokines in cellular processes that promote the development and progression of breast cancer warrants further understanding of the molecular basis for its actions to help guide the development of future therapeutic targets.en
dc.language.isoeng
dc.subjectIL-11en
dc.subjectIL-6en
dc.subjectSTAT3en
dc.subjectbreast canceren
dc.subjectmetastasisen
dc.subjecttargeted therapiesen
dc.titleSTAT3 Signaling in Breast Cancer: Multicellular Actions and Therapeutic Potential.en
dc.typeJournal Articleen
dc.identifier.journaltitleCancersen
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Heidelberg, VIC 3084, Australiaen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35053592/en
dc.identifier.doi10.3390/cancers14020429en
dc.type.contentTexten
dc.identifier.orcid0000-0002-1245-729Xen
dc.identifier.orcid0000-0002-6399-1177en
dc.identifier.pubmedid35053592
local.name.researcherChand, Ashwini L
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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