| Literature DB >> 28123924 |
Jessica L Bowser1, Russell R Broaddus2.
Abstract
The prevailing view of CD73 in cancer is that it is overexpressed in tumors and promotes cancer progression by dampening local T cell-mediated immune responses. We recently found that CD73 is down-regulated in poorly-differentiated and advanced stage endometrial carcinoma compared to normal endometrium and well-differentiated, early stage tumors. We revealed that CD73-generated adenosine induces a physiological response to protect epithelial integrity in well-differentiated, early stage endometrial carcinoma. The ability of CD73-generated adenosine to protect the barrier is not so different from its ability to induce immunosuppression and other physiological responses in cancerous tissues. In this commentary we examine the complexity of CD73 in cancer and suggest that a "one size fits all" approach to the role of CD73/adenosine in cancer is no longer warranted. Given that tumors often hijack normal cellular responses, we also provide consideration on how CD73s known role to protect barrier function may have implications in promoting tumor progression.Entities:
Keywords: CD73; actin polymerization; adenosine; adenosine receptors; barrier function; cancer; cell 15 adhesions; endometrium; epithelial integrity; tumor progression
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Year: 2016 PMID: 28123924 PMCID: PMC5214510 DOI: 10.1080/21688370.2016.1224963
Source DB: PubMed Journal: Tissue Barriers ISSN: 2168-8362