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Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma

This study investigated and verified the diagnostic and prognostic values of natural killer group 2 member D ligand (NKG2DL) genes in colon adenocarcinoma (COAD). We downloaded NKG2DLs expression data and corresponding clinical parameters from The Cancer Genome Atlas (TCGA) and used bioinformatics t...

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Autores principales: Ruan, Guo-Tian, Wang, Shuai, Zhu, Li-Chen, Liao, Xi-Wen, Wang, Xiang-Kun, Liao, Cun, Yan, Ling, Xie, Hai-Lun, Gong, Yi-Zhen, Gan, Jia-Liang, Gao, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148460/
https://www.ncbi.nlm.nih.gov/pubmed/33909599
http://dx.doi.org/10.18632/aging.202935
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author Ruan, Guo-Tian
Wang, Shuai
Zhu, Li-Chen
Liao, Xi-Wen
Wang, Xiang-Kun
Liao, Cun
Yan, Ling
Xie, Hai-Lun
Gong, Yi-Zhen
Gan, Jia-Liang
Gao, Feng
author_facet Ruan, Guo-Tian
Wang, Shuai
Zhu, Li-Chen
Liao, Xi-Wen
Wang, Xiang-Kun
Liao, Cun
Yan, Ling
Xie, Hai-Lun
Gong, Yi-Zhen
Gan, Jia-Liang
Gao, Feng
author_sort Ruan, Guo-Tian
collection PubMed
description This study investigated and verified the diagnostic and prognostic values of natural killer group 2 member D ligand (NKG2DL) genes in colon adenocarcinoma (COAD). We downloaded NKG2DLs expression data and corresponding clinical parameters from The Cancer Genome Atlas (TCGA) and used bioinformatics techniques to investigate the values of NKG2DLs in COAD. Then, we used the GSE40967 cohort to verify the prognostic value of NKG2DLs. Finally, we verified the ULBP2 expression level in tissues, and also investigated the diagnostic and prognostic values of ULBP2 in COAD. The diagnostic receiver operating characteristic curves showed that ULBP1, ULBP2, ULBP3, and RAET1L had high diagnostic values in COAD [Area Under Curve (AUC) > 0.9]. In TCGA cohort, the univariate and multivariate survival analyses suggested that ULBP2 was correlated with the prognosis of COAD recurrence-free survival (RFS) and overall survival (OS). In GSE40967 cohort, ULBP2 was associated with CC RFS and OS. Reverse transcription-quantitative polymerase chain reaction and immunohistochemistry results showed that ULBP2 was highly expressed in COAD tumor tissues (P < 0.05) and both had diagnostic values (AUC > 0.7). Validated survival analysis showed that the high expression of ULBP2 had a worse prognosis in COAD OS and RFS. Thus, ULBP2 might be an independent diagnostic and prognostic biomarker of COAD.
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spelling pubmed-81484602021-05-26 Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma Ruan, Guo-Tian Wang, Shuai Zhu, Li-Chen Liao, Xi-Wen Wang, Xiang-Kun Liao, Cun Yan, Ling Xie, Hai-Lun Gong, Yi-Zhen Gan, Jia-Liang Gao, Feng Aging (Albany NY) Research Paper This study investigated and verified the diagnostic and prognostic values of natural killer group 2 member D ligand (NKG2DL) genes in colon adenocarcinoma (COAD). We downloaded NKG2DLs expression data and corresponding clinical parameters from The Cancer Genome Atlas (TCGA) and used bioinformatics techniques to investigate the values of NKG2DLs in COAD. Then, we used the GSE40967 cohort to verify the prognostic value of NKG2DLs. Finally, we verified the ULBP2 expression level in tissues, and also investigated the diagnostic and prognostic values of ULBP2 in COAD. The diagnostic receiver operating characteristic curves showed that ULBP1, ULBP2, ULBP3, and RAET1L had high diagnostic values in COAD [Area Under Curve (AUC) > 0.9]. In TCGA cohort, the univariate and multivariate survival analyses suggested that ULBP2 was correlated with the prognosis of COAD recurrence-free survival (RFS) and overall survival (OS). In GSE40967 cohort, ULBP2 was associated with CC RFS and OS. Reverse transcription-quantitative polymerase chain reaction and immunohistochemistry results showed that ULBP2 was highly expressed in COAD tumor tissues (P < 0.05) and both had diagnostic values (AUC > 0.7). Validated survival analysis showed that the high expression of ULBP2 had a worse prognosis in COAD OS and RFS. Thus, ULBP2 might be an independent diagnostic and prognostic biomarker of COAD. Impact Journals 2021-04-27 /pmc/articles/PMC8148460/ /pubmed/33909599 http://dx.doi.org/10.18632/aging.202935 Text en Copyright: © 2021 Ruan et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ruan, Guo-Tian
Wang, Shuai
Zhu, Li-Chen
Liao, Xi-Wen
Wang, Xiang-Kun
Liao, Cun
Yan, Ling
Xie, Hai-Lun
Gong, Yi-Zhen
Gan, Jia-Liang
Gao, Feng
Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title_full Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title_fullStr Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title_full_unstemmed Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title_short Investigation and verification of the clinical significance and perspective of natural killer group 2 member D ligands in colon adenocarcinoma
title_sort investigation and verification of the clinical significance and perspective of natural killer group 2 member d ligands in colon adenocarcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148460/
https://www.ncbi.nlm.nih.gov/pubmed/33909599
http://dx.doi.org/10.18632/aging.202935
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