Cargando…

TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation

Pancreatic cancer is a lethal malignancy with a poor prognosis. This study aims to identify pancreatic cancer-related genes and develop a robust diagnostic model to detect this disease. Weighted gene co-expression network analysis (WGCNA) was used to determine potential hub genes for pancreatic canc...

Descripción completa

Detalles Bibliográficos
Autores principales: Ye, Hua, Li, Tiandong, Wang, Hua, Wu, Jinyu, Yi, Chuncheng, Shi, Jianxiang, Wang, Peng, Song, Chunhua, Dai, Liping, Jiang, Guozhong, Huang, Yuxin, Yu, Yongwei, Li, Jitian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015801/
https://www.ncbi.nlm.nih.gov/pubmed/33815409
http://dx.doi.org/10.3389/fimmu.2021.649551
_version_ 1783673748292894720
author Ye, Hua
Li, Tiandong
Wang, Hua
Wu, Jinyu
Yi, Chuncheng
Shi, Jianxiang
Wang, Peng
Song, Chunhua
Dai, Liping
Jiang, Guozhong
Huang, Yuxin
Yu, Yongwei
Li, Jitian
author_facet Ye, Hua
Li, Tiandong
Wang, Hua
Wu, Jinyu
Yi, Chuncheng
Shi, Jianxiang
Wang, Peng
Song, Chunhua
Dai, Liping
Jiang, Guozhong
Huang, Yuxin
Yu, Yongwei
Li, Jitian
author_sort Ye, Hua
collection PubMed
description Pancreatic cancer is a lethal malignancy with a poor prognosis. This study aims to identify pancreatic cancer-related genes and develop a robust diagnostic model to detect this disease. Weighted gene co-expression network analysis (WGCNA) was used to determine potential hub genes for pancreatic cancer. Their mRNA and protein expression levels were validated through reverse transcription PCR (RT-PCR) and immunohistochemical (IHC). Diagnostic models were developed by eight machine learning algorithms and ten-fold cross-validation. Four hub genes (TSPAN1, TMPRSS4, SDR16C5, and CTSE) were identified based on bioinformatics. RT-PCR showed that the four hub genes were expressed at medium to high levels, IHC revealed that their protein expression levels were higher in pancreatic cancer tissues. For the panel of these four genes, eight models performed with 0.87–0.92 area under the curve value (AUC), 0.91–0.94 sensitivity, and 0.84–0.86 specificity in the validation cohort. In the external validation set, these models also showed good performance (0.86–0.98 AUC, 0.84–1.00 sensitivity, and 0.86–1.00 specificity). In conclusion, this study has identified four hub genes that might be closely related to pancreatic cancer: TSPAN1, TMPRSS4, SDR16C5, and CTSE. Four-gene panels might provide a theoretical basis for the diagnosis of pancreatic cancer.
format Online
Article
Text
id pubmed-8015801
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-80158012021-04-02 TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation Ye, Hua Li, Tiandong Wang, Hua Wu, Jinyu Yi, Chuncheng Shi, Jianxiang Wang, Peng Song, Chunhua Dai, Liping Jiang, Guozhong Huang, Yuxin Yu, Yongwei Li, Jitian Front Immunol Immunology Pancreatic cancer is a lethal malignancy with a poor prognosis. This study aims to identify pancreatic cancer-related genes and develop a robust diagnostic model to detect this disease. Weighted gene co-expression network analysis (WGCNA) was used to determine potential hub genes for pancreatic cancer. Their mRNA and protein expression levels were validated through reverse transcription PCR (RT-PCR) and immunohistochemical (IHC). Diagnostic models were developed by eight machine learning algorithms and ten-fold cross-validation. Four hub genes (TSPAN1, TMPRSS4, SDR16C5, and CTSE) were identified based on bioinformatics. RT-PCR showed that the four hub genes were expressed at medium to high levels, IHC revealed that their protein expression levels were higher in pancreatic cancer tissues. For the panel of these four genes, eight models performed with 0.87–0.92 area under the curve value (AUC), 0.91–0.94 sensitivity, and 0.84–0.86 specificity in the validation cohort. In the external validation set, these models also showed good performance (0.86–0.98 AUC, 0.84–1.00 sensitivity, and 0.86–1.00 specificity). In conclusion, this study has identified four hub genes that might be closely related to pancreatic cancer: TSPAN1, TMPRSS4, SDR16C5, and CTSE. Four-gene panels might provide a theoretical basis for the diagnosis of pancreatic cancer. Frontiers Media S.A. 2021-03-18 /pmc/articles/PMC8015801/ /pubmed/33815409 http://dx.doi.org/10.3389/fimmu.2021.649551 Text en Copyright © 2021 Ye, Li, Wang, Wu, Yi, Shi, Wang, Song, Dai, Jiang, Huang, Yu and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ye, Hua
Li, Tiandong
Wang, Hua
Wu, Jinyu
Yi, Chuncheng
Shi, Jianxiang
Wang, Peng
Song, Chunhua
Dai, Liping
Jiang, Guozhong
Huang, Yuxin
Yu, Yongwei
Li, Jitian
TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title_full TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title_fullStr TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title_full_unstemmed TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title_short TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation
title_sort tspan1, tmprss4, sdr16c5, and ctse as novel panel for pancreatic cancer: a bioinformatics analysis and experiments validation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015801/
https://www.ncbi.nlm.nih.gov/pubmed/33815409
http://dx.doi.org/10.3389/fimmu.2021.649551
work_keys_str_mv AT yehua tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT litiandong tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT wanghua tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT wujinyu tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT yichuncheng tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT shijianxiang tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT wangpeng tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT songchunhua tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT dailiping tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT jiangguozhong tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT huangyuxin tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT yuyongwei tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation
AT lijitian tspan1tmprss4sdr16c5andctseasnovelpanelforpancreaticcancerabioinformaticsanalysisandexperimentsvalidation