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Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells

BACKGROUND: This study aimed to investigate the function and underlying molecular mechanism of N-α-acetyltransferase 10 protein (Naa10p) in cisplatin (CDDP) chemosensitivity in oral squamous cell carcinoma (OSCC). METHODS: Salivary Naa10p levels in 76 OSCC patients undergoing CDDP-based chemotherapy...

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Autores principales: Sun, Lichun, Wang, Kaixin, Peng, Lu, Zhang, Jinfang, Yang, Jie, Zhao, Juan, Xu, Jiang, Zheng, Jun, Zeng, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917391/
https://www.ncbi.nlm.nih.gov/pubmed/33658848
http://dx.doi.org/10.2147/CMAR.S296783
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author Sun, Lichun
Wang, Kaixin
Peng, Lu
Zhang, Jinfang
Yang, Jie
Zhao, Juan
Xu, Jiang
Zheng, Jun
Zeng, Yan
author_facet Sun, Lichun
Wang, Kaixin
Peng, Lu
Zhang, Jinfang
Yang, Jie
Zhao, Juan
Xu, Jiang
Zheng, Jun
Zeng, Yan
author_sort Sun, Lichun
collection PubMed
description BACKGROUND: This study aimed to investigate the function and underlying molecular mechanism of N-α-acetyltransferase 10 protein (Naa10p) in cisplatin (CDDP) chemosensitivity in oral squamous cell carcinoma (OSCC). METHODS: Salivary Naa10p levels in 76 OSCC patients undergoing CDDP-based chemotherapy were detected using enzyme-linked immunosorbent assay. Quantitative real-time polymerase chain reaction and Western blot were used to examine the expression of Naa10p in constructed CDDP-resistant OSCC cell (Cal-27/CDDP) lines and nude mouse model. In addition, the tumor volume and weight of nude mice were analyzed. Lentiviral system was employed to establish and identify OSCC cell lines with stable Naa10p interference or overexpression. MTT assay was used for drug sensitivity analysis. P-gp and Bcl-2 expression levels were tested by Western blot. RESULTS: Higher salivary Naa10p expression was present in the complete response/partial response group (n=46) compared to the stable disease/progressive disease group (n=30) in OSCC patients receiving chemotherapy treatment. Naa10p expression was down-regulated in Cal-27/CDDP cells and tissues. Naa10p overexpression significantly reduced the expression level of drug-resistant molecules. Naa10p was related to CDDP resistance and enhanced CDDP sensitivity in OSCC according to drug sensitivity analysis and nude mouse model experiments. CONCLUSION: Naa10p plays a tumor suppressor gene role and is associated with CDDP resistance in OSCC. It can enhance CDDP sensitivity in OSCC and may be a potential target for OSCC chemotherapy.
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spelling pubmed-79173912021-03-02 Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells Sun, Lichun Wang, Kaixin Peng, Lu Zhang, Jinfang Yang, Jie Zhao, Juan Xu, Jiang Zheng, Jun Zeng, Yan Cancer Manag Res Original Research BACKGROUND: This study aimed to investigate the function and underlying molecular mechanism of N-α-acetyltransferase 10 protein (Naa10p) in cisplatin (CDDP) chemosensitivity in oral squamous cell carcinoma (OSCC). METHODS: Salivary Naa10p levels in 76 OSCC patients undergoing CDDP-based chemotherapy were detected using enzyme-linked immunosorbent assay. Quantitative real-time polymerase chain reaction and Western blot were used to examine the expression of Naa10p in constructed CDDP-resistant OSCC cell (Cal-27/CDDP) lines and nude mouse model. In addition, the tumor volume and weight of nude mice were analyzed. Lentiviral system was employed to establish and identify OSCC cell lines with stable Naa10p interference or overexpression. MTT assay was used for drug sensitivity analysis. P-gp and Bcl-2 expression levels were tested by Western blot. RESULTS: Higher salivary Naa10p expression was present in the complete response/partial response group (n=46) compared to the stable disease/progressive disease group (n=30) in OSCC patients receiving chemotherapy treatment. Naa10p expression was down-regulated in Cal-27/CDDP cells and tissues. Naa10p overexpression significantly reduced the expression level of drug-resistant molecules. Naa10p was related to CDDP resistance and enhanced CDDP sensitivity in OSCC according to drug sensitivity analysis and nude mouse model experiments. CONCLUSION: Naa10p plays a tumor suppressor gene role and is associated with CDDP resistance in OSCC. It can enhance CDDP sensitivity in OSCC and may be a potential target for OSCC chemotherapy. Dove 2021-02-22 /pmc/articles/PMC7917391/ /pubmed/33658848 http://dx.doi.org/10.2147/CMAR.S296783 Text en © 2021 Sun et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Sun, Lichun
Wang, Kaixin
Peng, Lu
Zhang, Jinfang
Yang, Jie
Zhao, Juan
Xu, Jiang
Zheng, Jun
Zeng, Yan
Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title_full Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title_fullStr Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title_full_unstemmed Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title_short Naa10p Enhances Chemosensitivity to Cisplatin in Oral Squamous Cell Carcinoma Cells
title_sort naa10p enhances chemosensitivity to cisplatin in oral squamous cell carcinoma cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917391/
https://www.ncbi.nlm.nih.gov/pubmed/33658848
http://dx.doi.org/10.2147/CMAR.S296783
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