Cargando…

Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells

Oral squamous cell carcinoma (OSCC) is the most prevalent form of malignant tumour in the oral cavity and its early detection is critical for improving the prognosis of affected patients. The present study aimed to isolate and confirm exosomes derived from the supernatant of the OSCC cell line CAL-2...

Descripción completa

Detalles Bibliográficos
Autores principales: Jin, Jiajia, Huang, Zixiao, Lu, Xiaoyan, Wu, Shengrong, Jia, Mei'E, Li, Xin, Li, Zhiyong, He, Xiangyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400702/
https://www.ncbi.nlm.nih.gov/pubmed/32782555
http://dx.doi.org/10.3892/ol.2020.11764
_version_ 1783566423416635392
author Jin, Jiajia
Huang, Zixiao
Lu, Xiaoyan
Wu, Shengrong
Jia, Mei'E
Li, Xin
Li, Zhiyong
He, Xiangyi
author_facet Jin, Jiajia
Huang, Zixiao
Lu, Xiaoyan
Wu, Shengrong
Jia, Mei'E
Li, Xin
Li, Zhiyong
He, Xiangyi
author_sort Jin, Jiajia
collection PubMed
description Oral squamous cell carcinoma (OSCC) is the most prevalent form of malignant tumour in the oral cavity and its early detection is critical for improving the prognosis of affected patients. The present study aimed to isolate and confirm exosomes derived from the supernatant of the OSCC cell line CAL-27 and human oral epithelial cells (HOECs), analyze long non-coding RNA (lncRNA) expression profiles and determine the diagnostic value based on bioinformatics analyses. The results indicated that the particles isolated from the supernatant of CAL-27 and HOECs were either round or oval, had a size range of 30–150 nm and were enriched with ALG-2 interacting protein X (ALIX) and tumour susceptibility 101 proteins (TSG101). These characteristics confirmed that these particles were exosomes. Three lncRNAs (NR-026892.1, NR-126435.1 and NR-036586.1) were selected as potential diagnostic biomarkers for OSCC. The expression levels of the selected lncRNAs were significantly different in CAL-27-exo vs. HOEC-exo, as well as in whole cells (CAL-27 vs. HOECs) (P<0.001). The expression levels of the three lncRNAs confirmed by quantitative PCR were consistent with the sequencing data. In conclusion, various lncRNAs were aberrantly expressed between cancerous and non-cancerous exosomes, suggesting that they may serve as biomarkers for cancer.
format Online
Article
Text
id pubmed-7400702
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-74007022020-08-10 Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells Jin, Jiajia Huang, Zixiao Lu, Xiaoyan Wu, Shengrong Jia, Mei'E Li, Xin Li, Zhiyong He, Xiangyi Oncol Lett Articles Oral squamous cell carcinoma (OSCC) is the most prevalent form of malignant tumour in the oral cavity and its early detection is critical for improving the prognosis of affected patients. The present study aimed to isolate and confirm exosomes derived from the supernatant of the OSCC cell line CAL-27 and human oral epithelial cells (HOECs), analyze long non-coding RNA (lncRNA) expression profiles and determine the diagnostic value based on bioinformatics analyses. The results indicated that the particles isolated from the supernatant of CAL-27 and HOECs were either round or oval, had a size range of 30–150 nm and were enriched with ALG-2 interacting protein X (ALIX) and tumour susceptibility 101 proteins (TSG101). These characteristics confirmed that these particles were exosomes. Three lncRNAs (NR-026892.1, NR-126435.1 and NR-036586.1) were selected as potential diagnostic biomarkers for OSCC. The expression levels of the selected lncRNAs were significantly different in CAL-27-exo vs. HOEC-exo, as well as in whole cells (CAL-27 vs. HOECs) (P<0.001). The expression levels of the three lncRNAs confirmed by quantitative PCR were consistent with the sequencing data. In conclusion, various lncRNAs were aberrantly expressed between cancerous and non-cancerous exosomes, suggesting that they may serve as biomarkers for cancer. D.A. Spandidos 2020-09 2020-06-24 /pmc/articles/PMC7400702/ /pubmed/32782555 http://dx.doi.org/10.3892/ol.2020.11764 Text en Copyright: © Jin 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
Jin, Jiajia
Huang, Zixiao
Lu, Xiaoyan
Wu, Shengrong
Jia, Mei'E
Li, Xin
Li, Zhiyong
He, Xiangyi
Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title_full Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title_fullStr Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title_full_unstemmed Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title_short Bioinformatics analysis of aberrantly expressed exosomal lncRNAs in oral squamous cell carcinoma (CAL-27 vs. oral epithelial) cells
title_sort bioinformatics analysis of aberrantly expressed exosomal lncrnas in oral squamous cell carcinoma (cal-27 vs. oral epithelial) cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400702/
https://www.ncbi.nlm.nih.gov/pubmed/32782555
http://dx.doi.org/10.3892/ol.2020.11764
work_keys_str_mv AT jinjiajia bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT huangzixiao bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT luxiaoyan bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT wushengrong bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT jiameie bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT lixin bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT lizhiyong bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells
AT hexiangyi bioinformaticsanalysisofaberrantlyexpressedexosomallncrnasinoralsquamouscellcarcinomacal27vsoralepithelialcells