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MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer

The purpose of this study is to identify candidate genes that could predict prognosis of early-stage tongue squamous cell carcinoma (TSCC) and its occult cervical lymphatic metastasis by large-scale gene expression profiling. Tumor tissue and matched normal mucosa samples were collected from patient...

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Autores principales: Yang, Xi, Wu, Kailiu, Li, Siyi, Hu, Longwei, Han, Jing, Zhu, Dongwang, Tian, Xuerui, Liu, Wei, Tian, Zhen, Zhong, Laiping, Yan, Ming, Zhang, Chenping, Zhang, Zhiyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356821/
https://www.ncbi.nlm.nih.gov/pubmed/27713166
http://dx.doi.org/10.18632/oncotarget.12446
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author Yang, Xi
Wu, Kailiu
Li, Siyi
Hu, Longwei
Han, Jing
Zhu, Dongwang
Tian, Xuerui
Liu, Wei
Tian, Zhen
Zhong, Laiping
Yan, Ming
Zhang, Chenping
Zhang, Zhiyuan
author_facet Yang, Xi
Wu, Kailiu
Li, Siyi
Hu, Longwei
Han, Jing
Zhu, Dongwang
Tian, Xuerui
Liu, Wei
Tian, Zhen
Zhong, Laiping
Yan, Ming
Zhang, Chenping
Zhang, Zhiyuan
author_sort Yang, Xi
collection PubMed
description The purpose of this study is to identify candidate genes that could predict prognosis of early-stage tongue squamous cell carcinoma (TSCC) and its occult cervical lymphatic metastasis by large-scale gene expression profiling. Tumor tissue and matched normal mucosa samples were collected from patients with TSCC and analyzed with Affymetrix HTA2.0 high-density oligonucleotide array. Differentially expressed genes in TSCC with cervical lymph node metastasis (CLNM) were further analyzed with Gene Ontology and Kyoto Encyclopedia of Genes and Genomes for their functions and related pathways. A total of 107 differentially expressed genes (p < 0.05) were identified by microarray in TSCC samples with CLNM (n = 6) compared to those without CLNM (n = 6). Genes involved in the cell-matrix adherens junction and migration function including MFAP5, TNNC1, MGP, FBFBP1 and FBXO32 were selected and validated by RT-PCR in TSCC samples (n = 32). Of the five genes, MFAP5 and TNCC1 expressions were further validated by immohistochemistry (n = 61). The significant positive correlation between MFAP5 and TNNC1 expression (p<0.001) was observed. Notably, over-expression of MFAP5 and TNNC1 were correlated with CLNM, metastasis relapse-free survival and overall survival. Our findings indicated that MFAP5 and TNNC1 may be potential markers for predicting occult cervical lymphatic metastasis and prognosis of oral tongue carcinoma.
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spelling pubmed-53568212017-04-20 MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer Yang, Xi Wu, Kailiu Li, Siyi Hu, Longwei Han, Jing Zhu, Dongwang Tian, Xuerui Liu, Wei Tian, Zhen Zhong, Laiping Yan, Ming Zhang, Chenping Zhang, Zhiyuan Oncotarget Research Paper The purpose of this study is to identify candidate genes that could predict prognosis of early-stage tongue squamous cell carcinoma (TSCC) and its occult cervical lymphatic metastasis by large-scale gene expression profiling. Tumor tissue and matched normal mucosa samples were collected from patients with TSCC and analyzed with Affymetrix HTA2.0 high-density oligonucleotide array. Differentially expressed genes in TSCC with cervical lymph node metastasis (CLNM) were further analyzed with Gene Ontology and Kyoto Encyclopedia of Genes and Genomes for their functions and related pathways. A total of 107 differentially expressed genes (p < 0.05) were identified by microarray in TSCC samples with CLNM (n = 6) compared to those without CLNM (n = 6). Genes involved in the cell-matrix adherens junction and migration function including MFAP5, TNNC1, MGP, FBFBP1 and FBXO32 were selected and validated by RT-PCR in TSCC samples (n = 32). Of the five genes, MFAP5 and TNCC1 expressions were further validated by immohistochemistry (n = 61). The significant positive correlation between MFAP5 and TNNC1 expression (p<0.001) was observed. Notably, over-expression of MFAP5 and TNNC1 were correlated with CLNM, metastasis relapse-free survival and overall survival. Our findings indicated that MFAP5 and TNNC1 may be potential markers for predicting occult cervical lymphatic metastasis and prognosis of oral tongue carcinoma. Impact Journals LLC 2016-10-04 /pmc/articles/PMC5356821/ /pubmed/27713166 http://dx.doi.org/10.18632/oncotarget.12446 Text en Copyright: © 2017 Yang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Yang, Xi
Wu, Kailiu
Li, Siyi
Hu, Longwei
Han, Jing
Zhu, Dongwang
Tian, Xuerui
Liu, Wei
Tian, Zhen
Zhong, Laiping
Yan, Ming
Zhang, Chenping
Zhang, Zhiyuan
MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title_full MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title_fullStr MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title_full_unstemmed MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title_short MFAP5 and TNNC1: Potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
title_sort mfap5 and tnnc1: potential markers for predicting occult cervical lymphatic metastasis and prognosis in early stage tongue cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356821/
https://www.ncbi.nlm.nih.gov/pubmed/27713166
http://dx.doi.org/10.18632/oncotarget.12446
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