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LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS
Oral squamous cell carcinoma (OSCC) is a leading cause of cancer-related deaths worldwide, with 500 000 new cases each year. However, the mechanisms underlying OSCC development are relatively unknown. In this study, matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS)-ba...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636978/ https://www.ncbi.nlm.nih.gov/pubmed/28880263 http://dx.doi.org/10.1038/cddis.2017.433 |
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author | Yuan, Yao Xie, Xiaoyan Jiang, Yuchen Wei, Zihao Wang, Peiqi Chen, Fangman Li, Xinyi Sun, Chongkui Zhao, Hang Zeng, Xin Jiang, Lu Zhou, Yu Dan, Hongxia Feng, Mingye Liu, Rui Wang, Zhiyong Chen, Qianming |
author_facet | Yuan, Yao Xie, Xiaoyan Jiang, Yuchen Wei, Zihao Wang, Peiqi Chen, Fangman Li, Xinyi Sun, Chongkui Zhao, Hang Zeng, Xin Jiang, Lu Zhou, Yu Dan, Hongxia Feng, Mingye Liu, Rui Wang, Zhiyong Chen, Qianming |
author_sort | Yuan, Yao |
collection | PubMed |
description | Oral squamous cell carcinoma (OSCC) is a leading cause of cancer-related deaths worldwide, with 500 000 new cases each year. However, the mechanisms underlying OSCC development are relatively unknown. In this study, matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS)-based proteomic strategy was used to profile the differentially expressed peptides/proteins between OSCC tissues and their adjacent noncancerous tissues. Sixty-seven unique peptide peaks and five distinct proteins were identified with changed expression levels. Among them, LRP6 expression was found to be upregulated in OSCC tissues, and correlated with a cluster of clinicopathologic parameters, including smoking, drinking, tumor differentiation status, lymph node metastasis and survival time. Notably, knockdown of LRP6 inhibited the proliferation ability of OSCC cells. Furthermore, we demonstrated that the expression of LRP6 in OSCC cells is positively correlated with its downstream oncogene, FGF8. The present study suggests that LRP6 could be a potential biomarker for OSCC patients, and might further assist in the therapeutic decisions in OSCC treatment. |
format | Online Article Text |
id | pubmed-5636978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56369782017-10-12 LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS Yuan, Yao Xie, Xiaoyan Jiang, Yuchen Wei, Zihao Wang, Peiqi Chen, Fangman Li, Xinyi Sun, Chongkui Zhao, Hang Zeng, Xin Jiang, Lu Zhou, Yu Dan, Hongxia Feng, Mingye Liu, Rui Wang, Zhiyong Chen, Qianming Cell Death Dis Original Article Oral squamous cell carcinoma (OSCC) is a leading cause of cancer-related deaths worldwide, with 500 000 new cases each year. However, the mechanisms underlying OSCC development are relatively unknown. In this study, matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS)-based proteomic strategy was used to profile the differentially expressed peptides/proteins between OSCC tissues and their adjacent noncancerous tissues. Sixty-seven unique peptide peaks and five distinct proteins were identified with changed expression levels. Among them, LRP6 expression was found to be upregulated in OSCC tissues, and correlated with a cluster of clinicopathologic parameters, including smoking, drinking, tumor differentiation status, lymph node metastasis and survival time. Notably, knockdown of LRP6 inhibited the proliferation ability of OSCC cells. Furthermore, we demonstrated that the expression of LRP6 in OSCC cells is positively correlated with its downstream oncogene, FGF8. The present study suggests that LRP6 could be a potential biomarker for OSCC patients, and might further assist in the therapeutic decisions in OSCC treatment. Nature Publishing Group 2017-09 2017-09-07 /pmc/articles/PMC5636978/ /pubmed/28880263 http://dx.doi.org/10.1038/cddis.2017.433 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Yuan, Yao Xie, Xiaoyan Jiang, Yuchen Wei, Zihao Wang, Peiqi Chen, Fangman Li, Xinyi Sun, Chongkui Zhao, Hang Zeng, Xin Jiang, Lu Zhou, Yu Dan, Hongxia Feng, Mingye Liu, Rui Wang, Zhiyong Chen, Qianming LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title | LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title_full | LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title_fullStr | LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title_full_unstemmed | LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title_short | LRP6 is identified as a potential prognostic marker for oral squamous cell carcinoma via MALDI-IMS |
title_sort | lrp6 is identified as a potential prognostic marker for oral squamous cell carcinoma via maldi-ims |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636978/ https://www.ncbi.nlm.nih.gov/pubmed/28880263 http://dx.doi.org/10.1038/cddis.2017.433 |
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