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The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer

Devil Facial Tumour 2 (DFT2) is a recently discovered contagious cancer circulating in the Tasmanian devil (Sarcophilus harrisii), a species which already harbours a more widespread contagious cancer, Devil Facial Tumour 1 (DFT1). Here we show that in contrast to DFT1, DFT2 cells express major histo...

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Autores principales: Caldwell, Alison, Coleby, Rachel, Tovar, Cesar, Stammnitz, Maximilian R, Kwon, Young Mi, Owen, Rachel S, Tringides, Marios, Murchison, Elizabeth P, Skjødt, Karsten, Thomas, Gareth J, Kaufman, Jim, Elliott, Tim, Woods, Gregory M, Siddle, Hannah VT
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092122/
https://www.ncbi.nlm.nih.gov/pubmed/30103855
http://dx.doi.org/10.7554/eLife.35314
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author Caldwell, Alison
Coleby, Rachel
Tovar, Cesar
Stammnitz, Maximilian R
Kwon, Young Mi
Owen, Rachel S
Tringides, Marios
Murchison, Elizabeth P
Skjødt, Karsten
Thomas, Gareth J
Kaufman, Jim
Elliott, Tim
Woods, Gregory M
Siddle, Hannah VT
author_facet Caldwell, Alison
Coleby, Rachel
Tovar, Cesar
Stammnitz, Maximilian R
Kwon, Young Mi
Owen, Rachel S
Tringides, Marios
Murchison, Elizabeth P
Skjødt, Karsten
Thomas, Gareth J
Kaufman, Jim
Elliott, Tim
Woods, Gregory M
Siddle, Hannah VT
author_sort Caldwell, Alison
collection PubMed
description Devil Facial Tumour 2 (DFT2) is a recently discovered contagious cancer circulating in the Tasmanian devil (Sarcophilus harrisii), a species which already harbours a more widespread contagious cancer, Devil Facial Tumour 1 (DFT1). Here we show that in contrast to DFT1, DFT2 cells express major histocompatibility complex (MHC) class I molecules, demonstrating that loss of MHC is not necessary for the emergence of a contagious cancer. However, the most highly expressed MHC class I alleles in DFT2 cells are common among host devils or non-polymorphic, reducing immunogenicity in a population sharing these alleles. In parallel, MHC class I loss is emerging in vivo, thus DFT2 may be mimicking the evolutionary trajectory of DFT1. Based on these results we propose that contagious cancers may exploit partial histocompatibility between the tumour and host, but that loss of allogeneic antigens could facilitate widespread transmission of DFT2.
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spelling pubmed-60921222018-08-16 The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer Caldwell, Alison Coleby, Rachel Tovar, Cesar Stammnitz, Maximilian R Kwon, Young Mi Owen, Rachel S Tringides, Marios Murchison, Elizabeth P Skjødt, Karsten Thomas, Gareth J Kaufman, Jim Elliott, Tim Woods, Gregory M Siddle, Hannah VT eLife Cancer Biology Devil Facial Tumour 2 (DFT2) is a recently discovered contagious cancer circulating in the Tasmanian devil (Sarcophilus harrisii), a species which already harbours a more widespread contagious cancer, Devil Facial Tumour 1 (DFT1). Here we show that in contrast to DFT1, DFT2 cells express major histocompatibility complex (MHC) class I molecules, demonstrating that loss of MHC is not necessary for the emergence of a contagious cancer. However, the most highly expressed MHC class I alleles in DFT2 cells are common among host devils or non-polymorphic, reducing immunogenicity in a population sharing these alleles. In parallel, MHC class I loss is emerging in vivo, thus DFT2 may be mimicking the evolutionary trajectory of DFT1. Based on these results we propose that contagious cancers may exploit partial histocompatibility between the tumour and host, but that loss of allogeneic antigens could facilitate widespread transmission of DFT2. eLife Sciences Publications, Ltd 2018-08-14 /pmc/articles/PMC6092122/ /pubmed/30103855 http://dx.doi.org/10.7554/eLife.35314 Text en © 2018, Caldwell et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cancer Biology
Caldwell, Alison
Coleby, Rachel
Tovar, Cesar
Stammnitz, Maximilian R
Kwon, Young Mi
Owen, Rachel S
Tringides, Marios
Murchison, Elizabeth P
Skjødt, Karsten
Thomas, Gareth J
Kaufman, Jim
Elliott, Tim
Woods, Gregory M
Siddle, Hannah VT
The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title_full The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title_fullStr The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title_full_unstemmed The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title_short The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancer
title_sort newly-arisen devil facial tumour disease 2 (dft2) reveals a mechanism for the emergence of a contagious cancer
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092122/
https://www.ncbi.nlm.nih.gov/pubmed/30103855
http://dx.doi.org/10.7554/eLife.35314
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