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Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse

BACKGROUND: Keratins are structural marker proteins with tissue specific expression; however, recent reports indicate their involvement in cancer progression. Previous study from our lab revealed deregulation of many genes related to structural molecular integrity including KRT76. Here we evaluate t...

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Autores principales: Ambatipudi, Srikant, Bhosale, Priyanka G., Heath, Emma, Pandey, Manishkumar, Kumar, Gaurav, Kane, Shubhada, Patil, Asawari, Maru, Girish B., Desai, Rajiv S., Watt, Fiona M., Mahimkar, Manoj B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728316/
https://www.ncbi.nlm.nih.gov/pubmed/23936238
http://dx.doi.org/10.1371/journal.pone.0070688
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author Ambatipudi, Srikant
Bhosale, Priyanka G.
Heath, Emma
Pandey, Manishkumar
Kumar, Gaurav
Kane, Shubhada
Patil, Asawari
Maru, Girish B.
Desai, Rajiv S.
Watt, Fiona M.
Mahimkar, Manoj B.
author_facet Ambatipudi, Srikant
Bhosale, Priyanka G.
Heath, Emma
Pandey, Manishkumar
Kumar, Gaurav
Kane, Shubhada
Patil, Asawari
Maru, Girish B.
Desai, Rajiv S.
Watt, Fiona M.
Mahimkar, Manoj B.
author_sort Ambatipudi, Srikant
collection PubMed
description BACKGROUND: Keratins are structural marker proteins with tissue specific expression; however, recent reports indicate their involvement in cancer progression. Previous study from our lab revealed deregulation of many genes related to structural molecular integrity including KRT76. Here we evaluate the role of KRT76 downregulation in oral precancer and cancer development. METHODS: We evaluated KRT76 expression by qRT-PCR in normal and tumor tissues of the oral cavity. We also analyzed K76 expression by immunohistochemistry in normal, oral precancerous lesion (OPL), oral squamous cell carcinoma (OSCC) and in hamster model of oral carcinogenesis. Further, functional implication of KRT76 loss was confirmed using KRT76-knockout (KO) mice. RESULTS: We observed a strong association of reduced K76 expression with increased risk of OPL and OSCC development. The buccal epithelium of DMBA treated hamsters showed a similar trend. Oral cavity of KRT76-KO mice showed preneoplastic changes in the gingivobuccal epithelium while no pathological changes were observed in KRT76 negative tissues such as tongue. CONCLUSION: The present study demonstrates loss of KRT76 in oral carcinogenesis. The KRT76-KO mice data underlines the potential of KRT76 being an early event although this loss is not sufficient to drive the development of oral cancers. Thus, future studies to investigate the contributing role of KRT76 in light of other tumor driving events are warranted.
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spelling pubmed-37283162013-08-09 Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse Ambatipudi, Srikant Bhosale, Priyanka G. Heath, Emma Pandey, Manishkumar Kumar, Gaurav Kane, Shubhada Patil, Asawari Maru, Girish B. Desai, Rajiv S. Watt, Fiona M. Mahimkar, Manoj B. PLoS One Research Article BACKGROUND: Keratins are structural marker proteins with tissue specific expression; however, recent reports indicate their involvement in cancer progression. Previous study from our lab revealed deregulation of many genes related to structural molecular integrity including KRT76. Here we evaluate the role of KRT76 downregulation in oral precancer and cancer development. METHODS: We evaluated KRT76 expression by qRT-PCR in normal and tumor tissues of the oral cavity. We also analyzed K76 expression by immunohistochemistry in normal, oral precancerous lesion (OPL), oral squamous cell carcinoma (OSCC) and in hamster model of oral carcinogenesis. Further, functional implication of KRT76 loss was confirmed using KRT76-knockout (KO) mice. RESULTS: We observed a strong association of reduced K76 expression with increased risk of OPL and OSCC development. The buccal epithelium of DMBA treated hamsters showed a similar trend. Oral cavity of KRT76-KO mice showed preneoplastic changes in the gingivobuccal epithelium while no pathological changes were observed in KRT76 negative tissues such as tongue. CONCLUSION: The present study demonstrates loss of KRT76 in oral carcinogenesis. The KRT76-KO mice data underlines the potential of KRT76 being an early event although this loss is not sufficient to drive the development of oral cancers. Thus, future studies to investigate the contributing role of KRT76 in light of other tumor driving events are warranted. Public Library of Science 2013-07-30 /pmc/articles/PMC3728316/ /pubmed/23936238 http://dx.doi.org/10.1371/journal.pone.0070688 Text en © 2013 Ambatipudi 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ambatipudi, Srikant
Bhosale, Priyanka G.
Heath, Emma
Pandey, Manishkumar
Kumar, Gaurav
Kane, Shubhada
Patil, Asawari
Maru, Girish B.
Desai, Rajiv S.
Watt, Fiona M.
Mahimkar, Manoj B.
Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title_full Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title_fullStr Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title_full_unstemmed Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title_short Downregulation of Keratin 76 Expression during Oral Carcinogenesis of Human, Hamster and Mouse
title_sort downregulation of keratin 76 expression during oral carcinogenesis of human, hamster and mouse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728316/
https://www.ncbi.nlm.nih.gov/pubmed/23936238
http://dx.doi.org/10.1371/journal.pone.0070688
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