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Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer

INTRODUCTION: Colorectal cancer (CRC) is a common tumor with high morbidity and mortality. Current specific diagnosis regarding CRC remains complicated and costly, and specific diagnostic biomarkers are lacking. METHODS: To find potential diagnostic and prognostic biomarkers for CRC, we screened and...

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Autores principales: Lin, Kang, Zhu, Xiaojian, Luo, Chen, Bu, Fanqin, Zhu, Jinfeng, Zhu, Zhengming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860595/
https://www.ncbi.nlm.nih.gov/pubmed/33190424
http://dx.doi.org/10.1002/iid3.375
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author Lin, Kang
Zhu, Xiaojian
Luo, Chen
Bu, Fanqin
Zhu, Jinfeng
Zhu, Zhengming
author_facet Lin, Kang
Zhu, Xiaojian
Luo, Chen
Bu, Fanqin
Zhu, Jinfeng
Zhu, Zhengming
author_sort Lin, Kang
collection PubMed
description INTRODUCTION: Colorectal cancer (CRC) is a common tumor with high morbidity and mortality. Current specific diagnosis regarding CRC remains complicated and costly, and specific diagnostic biomarkers are lacking. METHODS: To find potential diagnostic and prognostic biomarkers for CRC, we screened and analyzed many CRC sequencing data by The Cancer Genome Atlas Program and Gene Expression Omnibus, and validated that CEP55 may be a potential diagnostic biomarker for CRC by molecular cytological experiments and immunohistochemistry, among others. RESULTS: We found that CEP55 is upregulated in CRC tissues and tumor cells and can promote CRC proliferation and metastasis by activating the p53/p21 axis and that CEP55 mutations in tumor patients result in worse overall survival and disease‐free survival time. Besides, we also found that genes, such as CDK1, CCNB1, NEK2, KIF14, CDCA5, and RFC3 were upregulated in tumors, and their mutations would affect the prognosis of CRC patients, but these results await for more experimental evidence. CONCLUSION: Our study validates CEP55 as a potential diagnostic and prognostic biomarker for CRC, and we also provide multiple genes and potential molecular mechanisms that may serve as diagnostic and prognostic markers for CRC.
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spelling pubmed-78605952021-02-05 Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer Lin, Kang Zhu, Xiaojian Luo, Chen Bu, Fanqin Zhu, Jinfeng Zhu, Zhengming Immun Inflamm Dis Original Research INTRODUCTION: Colorectal cancer (CRC) is a common tumor with high morbidity and mortality. Current specific diagnosis regarding CRC remains complicated and costly, and specific diagnostic biomarkers are lacking. METHODS: To find potential diagnostic and prognostic biomarkers for CRC, we screened and analyzed many CRC sequencing data by The Cancer Genome Atlas Program and Gene Expression Omnibus, and validated that CEP55 may be a potential diagnostic biomarker for CRC by molecular cytological experiments and immunohistochemistry, among others. RESULTS: We found that CEP55 is upregulated in CRC tissues and tumor cells and can promote CRC proliferation and metastasis by activating the p53/p21 axis and that CEP55 mutations in tumor patients result in worse overall survival and disease‐free survival time. Besides, we also found that genes, such as CDK1, CCNB1, NEK2, KIF14, CDCA5, and RFC3 were upregulated in tumors, and their mutations would affect the prognosis of CRC patients, but these results await for more experimental evidence. CONCLUSION: Our study validates CEP55 as a potential diagnostic and prognostic biomarker for CRC, and we also provide multiple genes and potential molecular mechanisms that may serve as diagnostic and prognostic markers for CRC. John Wiley and Sons Inc. 2020-11-15 /pmc/articles/PMC7860595/ /pubmed/33190424 http://dx.doi.org/10.1002/iid3.375 Text en © 2020 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lin, Kang
Zhu, Xiaojian
Luo, Chen
Bu, Fanqin
Zhu, Jinfeng
Zhu, Zhengming
Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title_full Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title_fullStr Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title_full_unstemmed Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title_short Data mining combined with experiments to validate CEP55 as a prognostic biomarker in colorectal cancer
title_sort data mining combined with experiments to validate cep55 as a prognostic biomarker in colorectal cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860595/
https://www.ncbi.nlm.nih.gov/pubmed/33190424
http://dx.doi.org/10.1002/iid3.375
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