Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm

Equine melanocytic neoplasm (EMN) is a cutaneous neoplasm and is mostly observed in aged grey horses. This preliminary study aimed to identify potential proteins to differentiate normal, mild and severe EMN from serum proteomic profiling. Serum samples were collected from 25 grey horses assigned to...

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Main Authors: Parichart Tesena, Amornthep Kingkaw, Wanwipa Vongsangnak, Surakiet Pitikarn, Narumon Phaonakrop, Sittiruk Roytrakul, Attawit Kovitvadhi
Other Authors: Kasetsart University
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Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/75633
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spelling th-mahidol.756332022-08-04T18:36:20Z Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm Parichart Tesena Amornthep Kingkaw Wanwipa Vongsangnak Surakiet Pitikarn Narumon Phaonakrop Sittiruk Roytrakul Attawit Kovitvadhi Kasetsart University Mahidol University Thailand National Center for Genetic Engineering and Biotechnology Agricultural and Biological Sciences Veterinary Equine melanocytic neoplasm (EMN) is a cutaneous neoplasm and is mostly observed in aged grey horses. This preliminary study aimed to identify potential proteins to differentiate normal, mild and severe EMN from serum proteomic profiling. Serum samples were collected from 25 grey horses assigned to three groups: normal (free of EMN; n = 10), mild (n = 6) and severe EMN (n = 9). To explore the differences in proteins between groups, proteomic profiling and analysis were employed. Accordingly, 8241 annotated proteins out of 8725 total proteins were compared between normal and EMN groups and inspected based on differentially expressed proteins (DEPs). Through DEP analysis, 95 significant DEPs differed between normal and EMN groups. Among these DEPs, 41 significant proteins were categorised according to protein functions. Based on 41 significant proteins, 10 were involved in metabolism and 31 in non-metabolism. Interestingly, phospholipid phosphatase6 (PLPP6) and ATPase subunit alpha (Na+/K+-ATPase) were considered as potential proteins uniquely expressed in mild EMN and related to lipid and energy metabolism, respectively. Non-metabolism-related proteins (BRCA1, phosphorylase B kinase regulatory subunit: PHKA1, tyrosine-protein kinase receptor: ALK and rho-associated protein kinase: ROCK1) correlated to melanoma development differed among all groups. The results of our study provide a foundation for early EMN biomonitoring and prevention. 2022-08-04T07:56:26Z 2022-08-04T07:56:26Z 2021-07-01 Article Animals. Vol.11, No.7 (2021) 10.3390/ani11071913 20762615 2-s2.0-85108621344 https://repository.li.mahidol.ac.th/handle/123456789/75633 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85108621344&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Agricultural and Biological Sciences
Veterinary
spellingShingle Agricultural and Biological Sciences
Veterinary
Parichart Tesena
Amornthep Kingkaw
Wanwipa Vongsangnak
Surakiet Pitikarn
Narumon Phaonakrop
Sittiruk Roytrakul
Attawit Kovitvadhi
Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
description Equine melanocytic neoplasm (EMN) is a cutaneous neoplasm and is mostly observed in aged grey horses. This preliminary study aimed to identify potential proteins to differentiate normal, mild and severe EMN from serum proteomic profiling. Serum samples were collected from 25 grey horses assigned to three groups: normal (free of EMN; n = 10), mild (n = 6) and severe EMN (n = 9). To explore the differences in proteins between groups, proteomic profiling and analysis were employed. Accordingly, 8241 annotated proteins out of 8725 total proteins were compared between normal and EMN groups and inspected based on differentially expressed proteins (DEPs). Through DEP analysis, 95 significant DEPs differed between normal and EMN groups. Among these DEPs, 41 significant proteins were categorised according to protein functions. Based on 41 significant proteins, 10 were involved in metabolism and 31 in non-metabolism. Interestingly, phospholipid phosphatase6 (PLPP6) and ATPase subunit alpha (Na+/K+-ATPase) were considered as potential proteins uniquely expressed in mild EMN and related to lipid and energy metabolism, respectively. Non-metabolism-related proteins (BRCA1, phosphorylase B kinase regulatory subunit: PHKA1, tyrosine-protein kinase receptor: ALK and rho-associated protein kinase: ROCK1) correlated to melanoma development differed among all groups. The results of our study provide a foundation for early EMN biomonitoring and prevention.
author2 Kasetsart University
author_facet Kasetsart University
Parichart Tesena
Amornthep Kingkaw
Wanwipa Vongsangnak
Surakiet Pitikarn
Narumon Phaonakrop
Sittiruk Roytrakul
Attawit Kovitvadhi
format Article
author Parichart Tesena
Amornthep Kingkaw
Wanwipa Vongsangnak
Surakiet Pitikarn
Narumon Phaonakrop
Sittiruk Roytrakul
Attawit Kovitvadhi
author_sort Parichart Tesena
title Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
title_short Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
title_full Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
title_fullStr Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
title_full_unstemmed Preliminary study: Proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
title_sort preliminary study: proteomic profiling uncovers potential proteins for biomonitoring equine melanocytic neoplasm
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/75633
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