pubmed-article:20127705 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C0025202 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C1704387 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C1522642 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C1979963 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C2003903 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:20127705 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:20127705 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:20127705 | pubmed:dateCreated | 2010-3-1 | lld:pubmed |
pubmed-article:20127705 | pubmed:abstractText | The intratumoral heterogeneity of cancer testis antigens (CTA) expression, which is driven by promoter methylation status, may hamper the effectiveness of CTA-directed vaccination of melanoma patients. Thus, we investigated whether the intratumoral heterogeneity of CTA expression is inherited at cellular level, or evolves throughout cellular replication, leading to a phenotypically unstable tumor cell population with reduced immunogenicity and/or able to escape immune control. Utilizing a previously characterized ex vivo clonal model of intratumoral heterogeneity of CTA expression in melanoma, Mel 313 MAGE-A3-low clone 5 (clone 5(M3-low)) and MAGE-A3-high clone 14 (clone 14(M3-high)) were sub-cloned and analyzed for CTA profile. Molecular assays demonstrated that levels of MAGE-A3 expression were highly conserved among generated sub-clones, as compared to parental clones. A similar behavior was identified for an extensive panel of other CTA investigated. Inherited levels of MAGE-A3 expression correlated with the extent of promoter methylation among clone 5(M3-low) and clone 14(M3-high) sub-clones analyzed. Treatment of clone 5(M3-low) with a DNA hypomethylating agent (DHA) resulted in an up-regulated expression of MAGE-A3, which was inherited at single cell level, being still detectable at day 60 in its sub-clones. Bisulfite sequencing demonstrated that also MAGE-A3 promoter methylation status was inherited among sub-clones generated from DHA-treated clone 5(M3-low) and strictly correlated with MAGE-A3 expression levels in investigated sub-clones. Similar results were obtained for additional CTA studied. Altogether our findings demonstrate that constitutive and DHA-modified CTA profiles of melanoma cells are clonally inherited throughout cellular replications, thus providing relevant insights to improve the effectiveness of CTA-based immunotherapy. | lld:pubmed |
pubmed-article:20127705 | pubmed:language | eng | lld:pubmed |
pubmed-article:20127705 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20127705 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20127705 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20127705 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20127705 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20127705 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:20127705 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20127705 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20127705 | pubmed:month | May | lld:pubmed |
pubmed-article:20127705 | pubmed:issn | 1097-4652 | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:FonsattiEster... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:SigalottiLuca... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:CalabròLuanaL | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:ColizziFrance... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:CoralSandraS | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:AltomonteMare... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:MaioMicheleM | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:FrattaElisabe... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:DanielliRicca... | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:CovreAlessiaA | lld:pubmed |
pubmed-article:20127705 | pubmed:author | pubmed-author:NicolayHugues... | lld:pubmed |
pubmed-article:20127705 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20127705 | pubmed:volume | 223 | lld:pubmed |
pubmed-article:20127705 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20127705 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20127705 | pubmed:pagination | 352-8 | lld:pubmed |
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pubmed-article:20127705 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20127705 | pubmed:articleTitle | Epigenetically regulated clonal heritability of CTA expression profiles in human melanoma. | lld:pubmed |
pubmed-article:20127705 | pubmed:affiliation | Cancer Bioimmunotherapy Unit, Centro di Riferimento Oncologico, Istituto di Ricovero e Cura a Carattere Scientifico, Aviano, PN, Italy. | lld:pubmed |
pubmed-article:20127705 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20127705 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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