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Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma

INTRODUCTION: Nasopharyngeal carcinoma (NPC) is a distinct type of head and neck cancer which is mostly prevalent in southern China. The development of NPC involves accumulation of multiple genetic changes. Chromosomal translocation is always thought to be accompanied with the fusion chimeric produc...

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Autores principales: Wang, Jing, Xie, Guo-Feng, He, Yuan, Deng, Ling, Long, Ya-Kang, Yang, Xin-Hua, Ma, Jiang-Jun, Gong, Rui, Cen, Wen-Jian, Ye, Zu-Lu, Zeng, Yi-Xin, Wang, Hai-Yun, Shao, Jian-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463592/
https://www.ncbi.nlm.nih.gov/pubmed/31057610
http://dx.doi.org/10.1155/2019/1654724
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author Wang, Jing
Xie, Guo-Feng
He, Yuan
Deng, Ling
Long, Ya-Kang
Yang, Xin-Hua
Ma, Jiang-Jun
Gong, Rui
Cen, Wen-Jian
Ye, Zu-Lu
Zeng, Yi-Xin
Wang, Hai-Yun
Shao, Jian-Yong
author_facet Wang, Jing
Xie, Guo-Feng
He, Yuan
Deng, Ling
Long, Ya-Kang
Yang, Xin-Hua
Ma, Jiang-Jun
Gong, Rui
Cen, Wen-Jian
Ye, Zu-Lu
Zeng, Yi-Xin
Wang, Hai-Yun
Shao, Jian-Yong
author_sort Wang, Jing
collection PubMed
description INTRODUCTION: Nasopharyngeal carcinoma (NPC) is a distinct type of head and neck cancer which is mostly prevalent in southern China. The development of NPC involves accumulation of multiple genetic changes. Chromosomal translocation is always thought to be accompanied with the fusion chimeric products. To data, the role of the fusion chimeric transcript remains obscure. MATERIALS AND METHODS: We performed RNA sequencing to detect the fusion genes in ten NPC tissues. Sanger sequencing and quantitative RT-PCR were used to measure the level of the fusion chimeric transcript in NPC tissues and cell lines. The functional experiments such as CCK8 assay, colony formation, and migration/invasion were conducted to analyze the role of this transcript in NPC in vitro. RESULTS: We demonstrated that the chimeric transcript SEPT7P2-PSPH was formed by trans-splicing of adjacent genes in the absence of chromosomal rearrangement and observed in both NPC patients and cell lines in parallel. Low-expression of the SEPT7P2-PSPH chimeric transcript induced the protein expression of PSPH and promoted cell proliferation, metastasis/invasion, and transforming ability in vitro. CONCLUSIONS: Our findings indicate that the chimeric transcript SEPT7P2-PSPH is a product of trans-splicing of two adjacent genes and might be a tumor suppressor gene, potentially having the role of anticancer activity.
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spelling pubmed-64635922019-05-05 Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma Wang, Jing Xie, Guo-Feng He, Yuan Deng, Ling Long, Ya-Kang Yang, Xin-Hua Ma, Jiang-Jun Gong, Rui Cen, Wen-Jian Ye, Zu-Lu Zeng, Yi-Xin Wang, Hai-Yun Shao, Jian-Yong J Oncol Research Article INTRODUCTION: Nasopharyngeal carcinoma (NPC) is a distinct type of head and neck cancer which is mostly prevalent in southern China. The development of NPC involves accumulation of multiple genetic changes. Chromosomal translocation is always thought to be accompanied with the fusion chimeric products. To data, the role of the fusion chimeric transcript remains obscure. MATERIALS AND METHODS: We performed RNA sequencing to detect the fusion genes in ten NPC tissues. Sanger sequencing and quantitative RT-PCR were used to measure the level of the fusion chimeric transcript in NPC tissues and cell lines. The functional experiments such as CCK8 assay, colony formation, and migration/invasion were conducted to analyze the role of this transcript in NPC in vitro. RESULTS: We demonstrated that the chimeric transcript SEPT7P2-PSPH was formed by trans-splicing of adjacent genes in the absence of chromosomal rearrangement and observed in both NPC patients and cell lines in parallel. Low-expression of the SEPT7P2-PSPH chimeric transcript induced the protein expression of PSPH and promoted cell proliferation, metastasis/invasion, and transforming ability in vitro. CONCLUSIONS: Our findings indicate that the chimeric transcript SEPT7P2-PSPH is a product of trans-splicing of two adjacent genes and might be a tumor suppressor gene, potentially having the role of anticancer activity. Hindawi 2019-04-01 /pmc/articles/PMC6463592/ /pubmed/31057610 http://dx.doi.org/10.1155/2019/1654724 Text en Copyright © 2019 Jing Wang et al. https://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
Wang, Jing
Xie, Guo-Feng
He, Yuan
Deng, Ling
Long, Ya-Kang
Yang, Xin-Hua
Ma, Jiang-Jun
Gong, Rui
Cen, Wen-Jian
Ye, Zu-Lu
Zeng, Yi-Xin
Wang, Hai-Yun
Shao, Jian-Yong
Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title_full Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title_fullStr Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title_full_unstemmed Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title_short Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with Nasopharyngeal Carcinoma
title_sort interfering expression of chimeric transcript sept7p2-psph promotes cell proliferation in patients with nasopharyngeal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463592/
https://www.ncbi.nlm.nih.gov/pubmed/31057610
http://dx.doi.org/10.1155/2019/1654724
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