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ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)

Devil Facial Tumour 1 (DFT1) is one of two transmissible neoplasms of Tasmanian devils (Sarcophilus harrisii) predominantly affecting their facial regions. DFT1’s cellular origin is that of Schwann cell lineage where lesions are evident macroscopically late in the disease. Conversely, the pre-clinic...

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Autores principales: Hayes, Dane A., Kunde, Dale A., Taylor, Robyn L., Pyecroft, Stephen B., Sohal, Sukhwinder Singh, Snow, Elizabeth T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462353/
https://www.ncbi.nlm.nih.gov/pubmed/28591206
http://dx.doi.org/10.1371/journal.pone.0177919
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author Hayes, Dane A.
Kunde, Dale A.
Taylor, Robyn L.
Pyecroft, Stephen B.
Sohal, Sukhwinder Singh
Snow, Elizabeth T.
author_facet Hayes, Dane A.
Kunde, Dale A.
Taylor, Robyn L.
Pyecroft, Stephen B.
Sohal, Sukhwinder Singh
Snow, Elizabeth T.
author_sort Hayes, Dane A.
collection PubMed
description Devil Facial Tumour 1 (DFT1) is one of two transmissible neoplasms of Tasmanian devils (Sarcophilus harrisii) predominantly affecting their facial regions. DFT1’s cellular origin is that of Schwann cell lineage where lesions are evident macroscopically late in the disease. Conversely, the pre-clinical timeframe from cellular transmission to appearance of DFT1 remains uncertain demonstrating the importance of an effective pre-clinical biomarker. We show that ERBB3, a marker expressed normally by the developing neural crest and Schwann cells, is immunohistohemically expressed by DFT1, therefore the potential of ERBB3 as a biomarker was explored. Under the hypothesis that serum ERBB3 levels may increase as DFT1 invades local and distant tissues our pilot study determined serum ERBB3 levels in normal Tasmanian devils and Tasmanian devils with DFT1. Compared to the baseline serum ERBB3 levels in unaffected Tasmanian devils, Tasmanian devils with DFT1 showed significant elevation of serum ERBB3 levels. Interestingly Tasmanian devils with cutaneous lymphoma (CL) also showed elevation of serum ERBB3 levels when compared to the baseline serum levels of Tasmanian devils without DFT1. Thus, elevated serum ERBB3 levels in otherwise healthy looking devils could predict possible DFT1 or CL in captive or wild devil populations and would have implications on the management, welfare and survival of Tasmanian devils. ERBB3 is also a therapeutic target and therefore the potential exists to consider modes of administration that may eradicate DFT1 from the wild.
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spelling pubmed-54623532017-06-22 ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1) Hayes, Dane A. Kunde, Dale A. Taylor, Robyn L. Pyecroft, Stephen B. Sohal, Sukhwinder Singh Snow, Elizabeth T. PLoS One Research Article Devil Facial Tumour 1 (DFT1) is one of two transmissible neoplasms of Tasmanian devils (Sarcophilus harrisii) predominantly affecting their facial regions. DFT1’s cellular origin is that of Schwann cell lineage where lesions are evident macroscopically late in the disease. Conversely, the pre-clinical timeframe from cellular transmission to appearance of DFT1 remains uncertain demonstrating the importance of an effective pre-clinical biomarker. We show that ERBB3, a marker expressed normally by the developing neural crest and Schwann cells, is immunohistohemically expressed by DFT1, therefore the potential of ERBB3 as a biomarker was explored. Under the hypothesis that serum ERBB3 levels may increase as DFT1 invades local and distant tissues our pilot study determined serum ERBB3 levels in normal Tasmanian devils and Tasmanian devils with DFT1. Compared to the baseline serum ERBB3 levels in unaffected Tasmanian devils, Tasmanian devils with DFT1 showed significant elevation of serum ERBB3 levels. Interestingly Tasmanian devils with cutaneous lymphoma (CL) also showed elevation of serum ERBB3 levels when compared to the baseline serum levels of Tasmanian devils without DFT1. Thus, elevated serum ERBB3 levels in otherwise healthy looking devils could predict possible DFT1 or CL in captive or wild devil populations and would have implications on the management, welfare and survival of Tasmanian devils. ERBB3 is also a therapeutic target and therefore the potential exists to consider modes of administration that may eradicate DFT1 from the wild. Public Library of Science 2017-06-07 /pmc/articles/PMC5462353/ /pubmed/28591206 http://dx.doi.org/10.1371/journal.pone.0177919 Text en © 2017 Hayes et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hayes, Dane A.
Kunde, Dale A.
Taylor, Robyn L.
Pyecroft, Stephen B.
Sohal, Sukhwinder Singh
Snow, Elizabeth T.
ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title_full ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title_fullStr ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title_full_unstemmed ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title_short ERBB3: A potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (DFT1)
title_sort erbb3: a potential serum biomarker for early detection and therapeutic target for devil facial tumour 1 (dft1)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462353/
https://www.ncbi.nlm.nih.gov/pubmed/28591206
http://dx.doi.org/10.1371/journal.pone.0177919
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