| pubmed-article:18612415 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0521119 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0007603 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0001480 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0024075 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0441889 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0475445 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C0205217 | lld:lifeskim |
| pubmed-article:18612415 | lifeskim:mentions | umls-concept:C1708481 | lld:lifeskim |
| pubmed-article:18612415 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:18612415 | pubmed:dateCreated | 2008-7-9 | lld:pubmed |
| pubmed-article:18612415 | pubmed:abstractText | There is growing awareness that tumour cells build up a "self-advantageous" microenvironment that reduces effectiveness of anti-tumour immune response. While many different immunosuppressive mechanisms are likely to come into play, recent evidence suggests that extracellular adenosine acting at A2A receptors may have a major role in down-modulating the immune response as cancerous tissues contain elevated levels of adenosine and adenosine break-down products. While there is no doubt that all cells possess plasma membrane adenosine transporters that mediate adenosine uptake and may also allow its release, it is now clear that most of extracellularly-generated adenosine originates from the catabolism of extracellular ATP. | lld:pubmed |
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| pubmed-article:18612415 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18612415 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18612415 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18612415 | pubmed:issn | 1932-6203 | lld:pubmed |
| pubmed-article:18612415 | pubmed:author | pubmed-author:PistoiaVitoV | lld:pubmed |
| pubmed-article:18612415 | pubmed:author | pubmed-author:Di... | lld:pubmed |
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| pubmed-article:18612415 | pubmed:author | pubmed-author:PellegattiPat... | lld:pubmed |
| pubmed-article:18612415 | pubmed:author | pubmed-author:PiccardiFeder... | lld:pubmed |
| pubmed-article:18612415 | pubmed:author | pubmed-author:BianchiGiovan... | lld:pubmed |
| pubmed-article:18612415 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18612415 | pubmed:volume | 3 | lld:pubmed |
| pubmed-article:18612415 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18612415 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18612415 | pubmed:pagination | e2599 | lld:pubmed |
| pubmed-article:18612415 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:18612415 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18612415 | pubmed:articleTitle | Increased level of extracellular ATP at tumor sites: in vivo imaging with plasma membrane luciferase. | lld:pubmed |
| pubmed-article:18612415 | pubmed:affiliation | Department of Experimental and Diagnostic Medicine, Section of General Pathology, Interdisciplinary Center for the Study of Inflammation, University of Ferrara, Ferrara, Italy. | lld:pubmed |
| pubmed-article:18612415 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18612415 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18612415 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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