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RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro
OBJECTIVE: Currently, many studies have found that RFC4 was up‐regulated in various cancers, and related to the progression and development. While the effects of RFC4 in oral tongue squamous cell carcinoma remain unclear, the main purpose of this research is to explore the role of RFC4 in oral tongu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128301/ https://www.ncbi.nlm.nih.gov/pubmed/33783864 http://dx.doi.org/10.1002/jcla.23761 |
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author | Zhang, Jian Wang, Linlin Xie, Xiao |
author_facet | Zhang, Jian Wang, Linlin Xie, Xiao |
author_sort | Zhang, Jian |
collection | PubMed |
description | OBJECTIVE: Currently, many studies have found that RFC4 was up‐regulated in various cancers, and related to the progression and development. While the effects of RFC4 in oral tongue squamous cell carcinoma remain unclear, the main purpose of this research is to explore the role of RFC4 in oral tongue squamous cell carcinoma. METHODS: The expression of RFC4 in various cancers was analyzed in GEPIA database, and the results were further verified by IHC assay. The relationship between RFC4 and several clinical parameters was analyzed; the proliferation was further observed by knockdown RFC4 in vitro. Finally, we constructed related nude mouse models by planting cells subcutaneous of nude mice, and the discrepancy was observed. RESULTS: Based on GEPIA database, RFC4 was up‐regulated in various cancers, including colorectal cancer, breast cancer, prostate cancer, lung cancer, and liver cancer. RFC4 was up‐regulated in oral tongue squamous cell carcinoma compared with the normal tissue from GEPIA online database; we further found that the expression of RFC4 was tightly associated with TNM stage (p = 0.005), but not with age, gender, and differentiation (p > 0.05). We further found that the proliferation of oral tongue squamous cell carcinoma was obviously restrained in vitro, and the carcinogenesis was also inhibited in vivo. CONCLUSIONS: We found that RFC4 was up‐regulated and related to the progression of oral tongue squamous cell carcinoma, and knockdown RFC4 could restrain the proliferation and progression. RFC4 might serve a potential biomarker and provide a new treatment strategy for lots of patients with oral tongue squamous cell carcinoma. |
format | Online Article Text |
id | pubmed-8128301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81283012021-05-21 RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro Zhang, Jian Wang, Linlin Xie, Xiao J Clin Lab Anal Research Articles OBJECTIVE: Currently, many studies have found that RFC4 was up‐regulated in various cancers, and related to the progression and development. While the effects of RFC4 in oral tongue squamous cell carcinoma remain unclear, the main purpose of this research is to explore the role of RFC4 in oral tongue squamous cell carcinoma. METHODS: The expression of RFC4 in various cancers was analyzed in GEPIA database, and the results were further verified by IHC assay. The relationship between RFC4 and several clinical parameters was analyzed; the proliferation was further observed by knockdown RFC4 in vitro. Finally, we constructed related nude mouse models by planting cells subcutaneous of nude mice, and the discrepancy was observed. RESULTS: Based on GEPIA database, RFC4 was up‐regulated in various cancers, including colorectal cancer, breast cancer, prostate cancer, lung cancer, and liver cancer. RFC4 was up‐regulated in oral tongue squamous cell carcinoma compared with the normal tissue from GEPIA online database; we further found that the expression of RFC4 was tightly associated with TNM stage (p = 0.005), but not with age, gender, and differentiation (p > 0.05). We further found that the proliferation of oral tongue squamous cell carcinoma was obviously restrained in vitro, and the carcinogenesis was also inhibited in vivo. CONCLUSIONS: We found that RFC4 was up‐regulated and related to the progression of oral tongue squamous cell carcinoma, and knockdown RFC4 could restrain the proliferation and progression. RFC4 might serve a potential biomarker and provide a new treatment strategy for lots of patients with oral tongue squamous cell carcinoma. John Wiley and Sons Inc. 2021-03-30 /pmc/articles/PMC8128301/ /pubmed/33783864 http://dx.doi.org/10.1002/jcla.23761 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, 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 | Research Articles Zhang, Jian Wang, Linlin Xie, Xiao RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title | RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title_full | RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title_fullStr | RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title_full_unstemmed | RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title_short | RFC4 promotes the progression and growth of Oral Tongue squamous cell carcinoma in vivo and vitro |
title_sort | rfc4 promotes the progression and growth of oral tongue squamous cell carcinoma in vivo and vitro |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128301/ https://www.ncbi.nlm.nih.gov/pubmed/33783864 http://dx.doi.org/10.1002/jcla.23761 |
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