Source:http://linkedlifedata.com/resource/pubmed/id/21317876
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0025202,
umls-concept:C0036525,
umls-concept:C0085295,
umls-concept:C0086035,
umls-concept:C0185117,
umls-concept:C0431085,
umls-concept:C0442038,
umls-concept:C0449258,
umls-concept:C0677930,
umls-concept:C1336956,
umls-concept:C1522484,
umls-concept:C1527148,
umls-concept:C2911684
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pubmed:issue |
6
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pubmed:dateCreated |
2011-6-1
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pubmed:abstractText |
Downregulation of the immune system facilitates tumor progression at different stages of cutaneous melanoma. Sentinel nodes, the first lymph nodes on lymphatics draining directly from a primary melanoma, are immune downregulated by tumor-generated immunosuppressive cytokines, including interleukin-10 (IL-10). To better understand the kinetics of sentinel node suppression, we investigated IL-10 expression by melanoma cells and tumor-associated macrophages and lymphocytes at different stages of primary melanoma evolution. We used reverse-transcriptase in situ PCR to identify the cellular sources of IL-10 mRNA in 39 melanomas. IL-10 mRNA was identified in tumor cells of 2 of 6 melanomas in situ (33%), of 17 of 21 invasive melanomas (81%) and of 11 of 12 metastatic melanomas (92%). Higher IL-10 expression correlates with tumor progression, with differences between melanoma in situ, invasive melanoma and metastatic melanoma. In primary melanomas, the IL-10 mRNA content of tumor cells correlates with Clark's level. There was significantly more IL-10 mRNA in vertical growth-phase melanoma cells than in radial growth-phase cells. In a logistic regression model, moderate-to-high IL-10 mRNA expression by tumor cells was significantly associated with vertical growth-phase melanoma. IL-10 mRNA was detected in melanoma-associated macrophages and lymphocytes. In invasive melanomas, IL-10 mRNA reactivity of macrophages decreased as Clark's level increased. Alterations of immunity by IL-10 derived from melanoma cells and melanoma-associated macrophages and lymphocytes potentially facilitate evolution of the primary melanoma and render regional lymph nodes susceptible to metastases.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1530-0285
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
801-9
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pubmed:meshHeading |
pubmed-meshheading:21317876-Disease Progression,
pubmed-meshheading:21317876-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:21317876-Humans,
pubmed-meshheading:21317876-Interleukin-10,
pubmed-meshheading:21317876-Lymphocytes, Tumor-Infiltrating,
pubmed-meshheading:21317876-Melanoma,
pubmed-meshheading:21317876-Neoplasm Invasiveness,
pubmed-meshheading:21317876-Nevus, Pigmented,
pubmed-meshheading:21317876-RNA, Messenger,
pubmed-meshheading:21317876-Skin Neoplasms,
pubmed-meshheading:21317876-Tumor Markers, Biological
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pubmed:year |
2011
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pubmed:articleTitle |
IL-10 expression by primary tumor cells correlates with melanoma progression from radial to vertical growth phase and development of metastatic competence.
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pubmed:affiliation |
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. itakura@ucla.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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