Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/18590
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DC Field | Value | Language |
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dc.contributor.author | Johnstone, Cameron N | - |
dc.contributor.author | Chand, Ashwini | - |
dc.contributor.author | Putoczki, Tracy L | - |
dc.contributor.author | Ernst, Matthias | - |
dc.date | 2015-07-14 | - |
dc.date.accessioned | 2018-08-30T06:23:39Z | - |
dc.date.available | 2018-08-30T06:23:39Z | - |
dc.date.issued | 2015-10 | - |
dc.identifier.citation | Cytokine & growth factor reviews 2015; 26(5): 489-98 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/18590 | - |
dc.description.abstract | Interleukin (IL)-11 is a member of the IL-6 family of cytokines that is defined by the shared use of the GP130 signal transducing receptor subunit. In addition of its long recognized activities as a hemopoietic growth factor, IL-11 has an emerging role in epithelial cancer biology. Through the activation of the GP130-Janus kinase signaling cascade and associated transcription factor STAT3, IL-11 can confer many of the tumor intrinsic 'hallmark' capabilities to neoplastic cells, if they express the ligand-specific IL-11Rα receptor subunit. Accordingly, IL-11 signaling has recently been identified as a rate-limiting step for the growth tumors arising from the mucosa of the gastrointestinal tract. However, there is less appreciation for a potential role of IL-11 to support breast cancer progression, apart from its well documented capacity to facilitate bone metastasis. Here we review evidence that IL-11 expression in breast cancer correlates with poor disease outcome and discuss some of the molecular mechanisms that are likely to underpin these observations. These include the capacity of IL-11 to stimulate survival and proliferation of cancer cells alongside angiogenesis of the primary tumor and of metastatic progenies at distant organs. We review current strategies to interfere with IL-11 signaling and advocate that inhibition of IL-11 signaling may represent an emerging therapeutic opportunity for numerous cancers. | - |
dc.language.iso | eng | - |
dc.subject | Cancer | - |
dc.subject | IL-11 | - |
dc.subject | IL-6 | - |
dc.subject | Interleukin | - |
dc.subject | STAT3 | - |
dc.title | Emerging roles for IL-11 signaling in cancer development and progression: Focus on breast cancer. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Cytokine & growth factor reviews | - |
dc.identifier.affiliation | Cancer & Inflammation Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | School of Cancer Medicine, LaTrobe University, Heidelberg, VIC 3084, Australia | - |
dc.identifier.affiliation | Department of Medical Biology, Melbourne University, Parkville, Victoria, Australia | - |
dc.identifier.affiliation | Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | Inflammation Division, Walter & Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia | en |
dc.identifier.affiliation | Cancer Metastasis Laboratory, Cancer Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia | en |
dc.identifier.doi | 10.1016/j.cytogfr.2015.07.015 | - |
dc.identifier.orcid | 0000-0002-6399-1177 | - |
dc.identifier.pubmedid | 26209885 | - |
dc.type.austin | Journal Article | - |
dc.type.austin | Research Support, Non-U.S. Gov't | - |
dc.type.austin | Review | - |
local.name.researcher | Ernst, Matthias | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
Appears in Collections: | Journal articles |
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