3.8 Article

Overexpression and extra-mitochondrial localization of the chaperonin Hsp60 in ameloblastoma

Journal

JOURNAL OF ORAL BIOSCIENCES
Volume 63, Issue 3, Pages 271-277

Publisher

ELSEVIER
DOI: 10.1016/j.job.2021.05.001

Keywords

Dentigerous cyst; Differential expression; Membrane proteins; Odontogenic tumors; Hsp60

Funding

  1. Consejo Nacional de Ciencia y Tecnologia (CONACyT, Mexico) [230110]

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The study aimed to identify differentially expressed membrane proteins in ameloblastomas and dentigerous cysts, with chaperonin Hsp60 identified as a potential target for ameloblastoma treatment due to its overexpression and possible involvement in ameloblastoma development.
Objectives: Ameloblastoma is an odontogenic neoplasm of the mandible and maxilla with various histological types and subtypes. It has been reported that some ameloblastomas could arise from dentigerous cyst walls; thus, the development of ameloblastoma from dentigerous cysts may be due to differential protein expression. Our aim was to identify a membrane protein that is differentially expressed in ameloblastomas with respect to dentigerous cysts. Methods: We analyzed the SDS-PAGE profiles of membrane proteins from ameloblastomas and dentigerous cysts. The protein in a band present in the ameloblastoma sample, but apparently absent in the dentigerous cyst sample was identified via mass spectrometry as the chaperonin Hsp60. We used western blotting and immunohistochemistry to analyze its overexpression and localization in ameloblastoma. Results: We found a differential band of 95 kDa in the membrane proteins of ameloblastoma. In this band, the chaperonin Hsp60 was identified, and its overexpression was corroborated using western blotting and immunohistochemistry. Hsp60 was localized in the plasma membrane of all ameloblastoma samples studied; in addition, it was found in the cell nucleus of the plexiform subtype of conventional ameloblastoma. Conclusions: Our results suggest that Hsp60 may be involved in ameloblastoma development, and could therefore be a potential therapeutic target for ameloblastoma treatment. (C) 2021 Japanese Association for Oral Biology. Published by Elsevier B.V. All rights reserved.

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