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UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma

Renal cell carcinoma (RCC) is a common malignant tumor globally. The overall survival of patients with RCC is poor; one important factor is tumor heterogeneity. Ubiquitin-conjugating enzyme E2T (UBE2T) has been reported to act as an oncogene in various types of cancer; however, its role in RCC has y...

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Autores principales: Hao, Peng, Kang, Bo, Li, Yapeng, Hao, Wenqi, Ma, Feihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625406/
https://www.ncbi.nlm.nih.gov/pubmed/31173226
http://dx.doi.org/10.3892/mmr.2019.10322
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author Hao, Peng
Kang, Bo
Li, Yapeng
Hao, Wenqi
Ma, Feihong
author_facet Hao, Peng
Kang, Bo
Li, Yapeng
Hao, Wenqi
Ma, Feihong
author_sort Hao, Peng
collection PubMed
description Renal cell carcinoma (RCC) is a common malignant tumor globally. The overall survival of patients with RCC is poor; one important factor is tumor heterogeneity. Ubiquitin-conjugating enzyme E2T (UBE2T) has been reported to act as an oncogene in various types of cancer; however, its role in RCC has yet to be investigated. In the present study, UBE2T was demonstrated via reverse transcription-quantitative PCR analysis to be significantly upregulated in RCC samples and cell lines compared with in normal tissue and cells. Additionally, UBE2T expression was significantly associated with late tumor stage and high grade in patients with RCC, and patients with high UBE2T expression exhibited poor prognosis compared with patients with low expression. Following knockdown of UBE2T in 786-O cells using RNA interference technology, the proliferation and colony formation of cells were inhibited as determined by an MTT assay and crystal violet staining, respectively; however, the migration and invasion of 786-O cells were not affected, as determined by wound-healing assay and Transwell assays, respectively. Xenograft RCC tumor growth in vivo was also significantly suppressed. The expression levels of two mesenchymal cell markers, N-cadherin and vimentin, were reduced following UBE2T knockdown, whereas E-cadherin and fibronectin levels were increased as determined by western blotting, indicating that epithelial-mesenchymal transition was suppressed. In addition, the phosphorylation levels of PI3K, Akt and mTOR were notably decreased following UBE2T knockdown, but were increased when UBE2T was overexpressed. Wortmannin, an Akt inhibitor, reversed the UBE2T overexpression-induced increase in the phosphorylation of PI3K, Akt and mTOR. Similarly, the UBE2T overexpression-induced promotion of 786-O cell proliferation was also attenuated by wortmannin. In conclusion, UBE2T promoted the proliferation of RCC cells by regulating PI3K/Akt signaling, suggesting it may be a novel target for the treatment of patients with RCC.
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spelling pubmed-66254062019-07-31 UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma Hao, Peng Kang, Bo Li, Yapeng Hao, Wenqi Ma, Feihong Mol Med Rep Articles Renal cell carcinoma (RCC) is a common malignant tumor globally. The overall survival of patients with RCC is poor; one important factor is tumor heterogeneity. Ubiquitin-conjugating enzyme E2T (UBE2T) has been reported to act as an oncogene in various types of cancer; however, its role in RCC has yet to be investigated. In the present study, UBE2T was demonstrated via reverse transcription-quantitative PCR analysis to be significantly upregulated in RCC samples and cell lines compared with in normal tissue and cells. Additionally, UBE2T expression was significantly associated with late tumor stage and high grade in patients with RCC, and patients with high UBE2T expression exhibited poor prognosis compared with patients with low expression. Following knockdown of UBE2T in 786-O cells using RNA interference technology, the proliferation and colony formation of cells were inhibited as determined by an MTT assay and crystal violet staining, respectively; however, the migration and invasion of 786-O cells were not affected, as determined by wound-healing assay and Transwell assays, respectively. Xenograft RCC tumor growth in vivo was also significantly suppressed. The expression levels of two mesenchymal cell markers, N-cadherin and vimentin, were reduced following UBE2T knockdown, whereas E-cadherin and fibronectin levels were increased as determined by western blotting, indicating that epithelial-mesenchymal transition was suppressed. In addition, the phosphorylation levels of PI3K, Akt and mTOR were notably decreased following UBE2T knockdown, but were increased when UBE2T was overexpressed. Wortmannin, an Akt inhibitor, reversed the UBE2T overexpression-induced increase in the phosphorylation of PI3K, Akt and mTOR. Similarly, the UBE2T overexpression-induced promotion of 786-O cell proliferation was also attenuated by wortmannin. In conclusion, UBE2T promoted the proliferation of RCC cells by regulating PI3K/Akt signaling, suggesting it may be a novel target for the treatment of patients with RCC. D.A. Spandidos 2019-08 2019-06-03 /pmc/articles/PMC6625406/ /pubmed/31173226 http://dx.doi.org/10.3892/mmr.2019.10322 Text en Copyright: © Hao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Hao, Peng
Kang, Bo
Li, Yapeng
Hao, Wenqi
Ma, Feihong
UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title_full UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title_fullStr UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title_full_unstemmed UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title_short UBE2T promotes proliferation and regulates PI3K/Akt signaling in renal cell carcinoma
title_sort ube2t promotes proliferation and regulates pi3k/akt signaling in renal cell carcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625406/
https://www.ncbi.nlm.nih.gov/pubmed/31173226
http://dx.doi.org/10.3892/mmr.2019.10322
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