FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA

Objective To research the expression levels of FEN1 and PCNA in carcinoma ⁃ associated fibroblasts (CAFs) and analyze their correlation. Methods Fresh specimens of oral squamous cell carcinoma tissues and normal oral mucosal tissues excised during oral and maxillofacial plastic surgery were collec...

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Main Author: ZHOU Hongmei
Format: Article
Language:zho
Published: Editorial Department of Journal of Prevention and Treatment for Stomatological Diseases 2018-06-01
Series:口腔疾病防治
Subjects:
Online Access:http://www.kqjbfz.com/EN/10.12016/j.issn.2096-1456.2018.06.003
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author ZHOU Hongmei
author_facet ZHOU Hongmei
author_sort ZHOU Hongmei
collection DOAJ
description Objective To research the expression levels of FEN1 and PCNA in carcinoma ⁃ associated fibroblasts (CAFs) and analyze their correlation. Methods Fresh specimens of oral squamous cell carcinoma tissues and normal oral mucosal tissues excised during oral and maxillofacial plastic surgery were collected. Primary oral CAFs and normal fibroblasts (NFs) were obtained by tissue culture, identified by immunocytochemistry and divided into the CAF and NF groups. Western blot and quantitative real ⁃time PCR were used to detect the protein and mRNA expression levels of both FEN1 and PCNA in the oral CAFs and NFs. The correlation between FEN1 and PCNA expression in oral CAFs was analyzed. Results Oral CAFs and oral NFs were successfully cultured and identified from 12 samples. Both the protein and mRNA expression levels of FEN1 and PCNA were higher in the oral CAFs than NFs, but there were no sig⁃ nificant differences (P > 0.05). In the oral CAFs, the linear correlation coefficient between FEN1 and PCNA was 0.677 (P = 0.016) at the mRNA level, indicating a strong positive correlation; however, at the protein level, no correlation was found (P > 0.05). Conclusion In primary cultured oral CAFs and NFs, there were no significant differences in the FEN1 and PCNA protein and mRNA expression levels. However, in the CAFs, the mRNA levels of FEN1 and PCNA had a strong positive correlation. The relationship and the regulatory mechanism of the two genes require further study.
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spelling doaj.art-e4452a97bf4d4ae7b63955e6afe89d872022-12-22T03:10:16ZzhoEditorial Department of Journal of Prevention and Treatment for Stomatological Diseases口腔疾病防治2096-14562096-14562018-06-0126635435910.12016/j.issn.2096⁃1456.2018.06.003FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA ZHOU Hongmei0State Key Laboratory of Oral Diseas⁃ es, Department of Oral Medicine, West China Hospital of Stomatology, Sichuan UniversityObjective To research the expression levels of FEN1 and PCNA in carcinoma ⁃ associated fibroblasts (CAFs) and analyze their correlation. Methods Fresh specimens of oral squamous cell carcinoma tissues and normal oral mucosal tissues excised during oral and maxillofacial plastic surgery were collected. Primary oral CAFs and normal fibroblasts (NFs) were obtained by tissue culture, identified by immunocytochemistry and divided into the CAF and NF groups. Western blot and quantitative real ⁃time PCR were used to detect the protein and mRNA expression levels of both FEN1 and PCNA in the oral CAFs and NFs. The correlation between FEN1 and PCNA expression in oral CAFs was analyzed. Results Oral CAFs and oral NFs were successfully cultured and identified from 12 samples. Both the protein and mRNA expression levels of FEN1 and PCNA were higher in the oral CAFs than NFs, but there were no sig⁃ nificant differences (P > 0.05). In the oral CAFs, the linear correlation coefficient between FEN1 and PCNA was 0.677 (P = 0.016) at the mRNA level, indicating a strong positive correlation; however, at the protein level, no correlation was found (P > 0.05). Conclusion In primary cultured oral CAFs and NFs, there were no significant differences in the FEN1 and PCNA protein and mRNA expression levels. However, in the CAFs, the mRNA levels of FEN1 and PCNA had a strong positive correlation. The relationship and the regulatory mechanism of the two genes require further study.http://www.kqjbfz.com/EN/10.12016/j.issn.2096-1456.2018.06.003Carcinoma ⁃ associated fibroblastsFlap endonuclease ⁃ 1Proliferating cell nuclear antigenEx⁃ pression levelOral cavity
spellingShingle ZHOU Hongmei
FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
口腔疾病防治
Carcinoma ⁃ associated fibroblasts
Flap endonuclease ⁃ 1
Proliferating cell nuclear antigen
Ex⁃ pression level
Oral cavity
title FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
title_full FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
title_fullStr FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
title_full_unstemmed FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
title_short FEN1 expression in oral carcinoma⁃associated fibroblasts and its relationship with PCNA
title_sort fen1 expression in oral carcinoma⁃associated fibroblasts and its relationship with pcna
topic Carcinoma ⁃ associated fibroblasts
Flap endonuclease ⁃ 1
Proliferating cell nuclear antigen
Ex⁃ pression level
Oral cavity
url http://www.kqjbfz.com/EN/10.12016/j.issn.2096-1456.2018.06.003
work_keys_str_mv AT zhouhongmei fen1expressioninoralcarcinomaassociatedfibroblastsanditsrelationshipwithpcna