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Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma

OBJECTIVE: Oral squamous cell carcinoma (OSCC) is the most common cancer of the head and neck region. The circular RNA (circRNA) is known to serve an important role in the carcinogenesis of different types of cancer. However, the circRNA role of OSCC remains unclear. METHODS: 8 pairs of OSCC tissues...

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Autores principales: Li, Bowen, Wang, Feng, Li, Xiang, Sun, Shuai, Shen, Yuehong, Yang, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174780/
https://www.ncbi.nlm.nih.gov/pubmed/30344795
http://dx.doi.org/10.1155/2018/7496890
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author Li, Bowen
Wang, Feng
Li, Xiang
Sun, Shuai
Shen, Yuehong
Yang, Hongyu
author_facet Li, Bowen
Wang, Feng
Li, Xiang
Sun, Shuai
Shen, Yuehong
Yang, Hongyu
author_sort Li, Bowen
collection PubMed
description OBJECTIVE: Oral squamous cell carcinoma (OSCC) is the most common cancer of the head and neck region. The circular RNA (circRNA) is known to serve an important role in the carcinogenesis of different types of cancer. However, the circRNA role of OSCC remains unclear. METHODS: 8 pairs of OSCC tissues and adjacent normal tissues were obtained to detect circRNAs expression by high-throughput sequencing, and 45 pairs of OSCC tissues were selected to verify the differentially significant circRNAs by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). To further investigate the role of hsa_circ_0008309, the circRNA-microRNA (miR)-mRNA network was predicted using bioinformatics databases. The expression levels of hsa_circ_0008309, miR-1290, miR-136-5P, and miR-382-5P in SCC-15 and CAL27 cell lines were detected by RT-qPCR. Western blotting was performed to detect the protein level of Ataxin 1 (ATXN1). RESULTS: The high-throughput sequencing results demonstrated that circRNAs were abundantly expressed in OSCC, and 16 circRNAs were significantly differentially expressed. Hsa_circ_0008309 was significantly downregulated in 45 pairs of OSCC tissue samples and was statistically correlated with pathological differentiation. The bioinformatics databases suggested that hsa_circ_0008309 could combine with miR-1290, miR-136-5P, and miR-382-5P, respectively, to regulate the expression of ATXN1. It was subsequently identified that hsa_circ_0008309 may inhibit miR-136-5P and miR-382-5P expression and increase ATXN1 expression in the OSCC cell lines. CONCLUSION: In summary, the results of the present study revealed that OSCC tissues have abundant circRNAs and, to the best of our knowledge, we firstly explore the regulatory role of the hsa_circ_0008309-miR-136-5P/hsa-miR-382-5P-ATXN1 network in OSCC. The results indicated that hsa_circ_0008309 may be a potential biomarker for OSCC.
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spelling pubmed-61747802018-10-21 Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma Li, Bowen Wang, Feng Li, Xiang Sun, Shuai Shen, Yuehong Yang, Hongyu Dis Markers Research Article OBJECTIVE: Oral squamous cell carcinoma (OSCC) is the most common cancer of the head and neck region. The circular RNA (circRNA) is known to serve an important role in the carcinogenesis of different types of cancer. However, the circRNA role of OSCC remains unclear. METHODS: 8 pairs of OSCC tissues and adjacent normal tissues were obtained to detect circRNAs expression by high-throughput sequencing, and 45 pairs of OSCC tissues were selected to verify the differentially significant circRNAs by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). To further investigate the role of hsa_circ_0008309, the circRNA-microRNA (miR)-mRNA network was predicted using bioinformatics databases. The expression levels of hsa_circ_0008309, miR-1290, miR-136-5P, and miR-382-5P in SCC-15 and CAL27 cell lines were detected by RT-qPCR. Western blotting was performed to detect the protein level of Ataxin 1 (ATXN1). RESULTS: The high-throughput sequencing results demonstrated that circRNAs were abundantly expressed in OSCC, and 16 circRNAs were significantly differentially expressed. Hsa_circ_0008309 was significantly downregulated in 45 pairs of OSCC tissue samples and was statistically correlated with pathological differentiation. The bioinformatics databases suggested that hsa_circ_0008309 could combine with miR-1290, miR-136-5P, and miR-382-5P, respectively, to regulate the expression of ATXN1. It was subsequently identified that hsa_circ_0008309 may inhibit miR-136-5P and miR-382-5P expression and increase ATXN1 expression in the OSCC cell lines. CONCLUSION: In summary, the results of the present study revealed that OSCC tissues have abundant circRNAs and, to the best of our knowledge, we firstly explore the regulatory role of the hsa_circ_0008309-miR-136-5P/hsa-miR-382-5P-ATXN1 network in OSCC. The results indicated that hsa_circ_0008309 may be a potential biomarker for OSCC. Hindawi 2018-09-23 /pmc/articles/PMC6174780/ /pubmed/30344795 http://dx.doi.org/10.1155/2018/7496890 Text en Copyright © 2018 Bowen Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Bowen
Wang, Feng
Li, Xiang
Sun, Shuai
Shen, Yuehong
Yang, Hongyu
Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title_full Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title_fullStr Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title_full_unstemmed Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title_short Hsa_circ_0008309 May Be a Potential Biomarker for Oral Squamous Cell Carcinoma
title_sort hsa_circ_0008309 may be a potential biomarker for oral squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174780/
https://www.ncbi.nlm.nih.gov/pubmed/30344795
http://dx.doi.org/10.1155/2018/7496890
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