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Melanoma-restricted genes
Human metastatic cutaneous melanoma has gained a well deserved reputation for its immune responsiveness. The reason(s) remain(s) unknown. We attempted previously to characterize several variables that may affect the relationship between tumor and host immune cells but, taken one at the time, none yi...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC527872/ https://www.ncbi.nlm.nih.gov/pubmed/15488140 http://dx.doi.org/10.1186/1479-5876-2-34 |
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author | Wang, Ena Panelli, Monica C Zavaglia, Katia Mandruzzato, Susanna Hu, Nan Taylor, Phil R Seliger, Barbara Zanovello, Paola Freedman, Ralph S Marincola, Francesco M |
author_facet | Wang, Ena Panelli, Monica C Zavaglia, Katia Mandruzzato, Susanna Hu, Nan Taylor, Phil R Seliger, Barbara Zanovello, Paola Freedman, Ralph S Marincola, Francesco M |
author_sort | Wang, Ena |
collection | PubMed |
description | Human metastatic cutaneous melanoma has gained a well deserved reputation for its immune responsiveness. The reason(s) remain(s) unknown. We attempted previously to characterize several variables that may affect the relationship between tumor and host immune cells but, taken one at the time, none yielded a convincing explanation. With explorative purposes, high-throughput technology was applied here to portray transcriptional characteristics unique to metastatic cutaneous melanoma that may or may not be relevant to its immunogenic potential. Several functional signatures could be identified descriptive of immune or other biological functions. In addition, the transcriptional profile of metastatic melanoma was compared with that of primary renal cell cancers (RCC) identifying several genes co-coordinately expressed by the two tumor types. Since RCC is another immune responsive tumor, commonalities between RCC and melanoma may help untangle the enigma of their potential immune responsiveness. This purely descriptive study provides, therefore, a map for the investigation of metastatic melanoma in future clinical trials and at the same time may invite consideration of novel therapeutic targets. |
format | Text |
id | pubmed-527872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5278722004-11-14 Melanoma-restricted genes Wang, Ena Panelli, Monica C Zavaglia, Katia Mandruzzato, Susanna Hu, Nan Taylor, Phil R Seliger, Barbara Zanovello, Paola Freedman, Ralph S Marincola, Francesco M J Transl Med Research Human metastatic cutaneous melanoma has gained a well deserved reputation for its immune responsiveness. The reason(s) remain(s) unknown. We attempted previously to characterize several variables that may affect the relationship between tumor and host immune cells but, taken one at the time, none yielded a convincing explanation. With explorative purposes, high-throughput technology was applied here to portray transcriptional characteristics unique to metastatic cutaneous melanoma that may or may not be relevant to its immunogenic potential. Several functional signatures could be identified descriptive of immune or other biological functions. In addition, the transcriptional profile of metastatic melanoma was compared with that of primary renal cell cancers (RCC) identifying several genes co-coordinately expressed by the two tumor types. Since RCC is another immune responsive tumor, commonalities between RCC and melanoma may help untangle the enigma of their potential immune responsiveness. This purely descriptive study provides, therefore, a map for the investigation of metastatic melanoma in future clinical trials and at the same time may invite consideration of novel therapeutic targets. BioMed Central 2004-10-15 /pmc/articles/PMC527872/ /pubmed/15488140 http://dx.doi.org/10.1186/1479-5876-2-34 Text en Copyright © 2004 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wang, Ena Panelli, Monica C Zavaglia, Katia Mandruzzato, Susanna Hu, Nan Taylor, Phil R Seliger, Barbara Zanovello, Paola Freedman, Ralph S Marincola, Francesco M Melanoma-restricted genes |
title | Melanoma-restricted genes |
title_full | Melanoma-restricted genes |
title_fullStr | Melanoma-restricted genes |
title_full_unstemmed | Melanoma-restricted genes |
title_short | Melanoma-restricted genes |
title_sort | melanoma-restricted genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC527872/ https://www.ncbi.nlm.nih.gov/pubmed/15488140 http://dx.doi.org/10.1186/1479-5876-2-34 |
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