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Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer

BACKGROUND: Neurotrophic tropomyosin receptor kinases (NTRKs) are a gene family function as oncogene or tumor suppressor gene in distinct cancers. We aimed to investigate the methylation and expression profiles and prognostic value of NTRKs gene in colorectal cancer (CRC). METHODS: An analysis of DN...

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Autores principales: Chen, Zijian, Huang, Zenghong, Luo, Yanxin, Zou, Qi, Bai, Liangliang, Tang, Guannan, Wang, Xiaolin, Cao, Guangwen, Huang, Meijin, Xiang, Jun, Yu, Huichuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885252/
https://www.ncbi.nlm.nih.gov/pubmed/33593392
http://dx.doi.org/10.1186/s12967-021-02740-6
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author Chen, Zijian
Huang, Zenghong
Luo, Yanxin
Zou, Qi
Bai, Liangliang
Tang, Guannan
Wang, Xiaolin
Cao, Guangwen
Huang, Meijin
Xiang, Jun
Yu, Huichuan
author_facet Chen, Zijian
Huang, Zenghong
Luo, Yanxin
Zou, Qi
Bai, Liangliang
Tang, Guannan
Wang, Xiaolin
Cao, Guangwen
Huang, Meijin
Xiang, Jun
Yu, Huichuan
author_sort Chen, Zijian
collection PubMed
description BACKGROUND: Neurotrophic tropomyosin receptor kinases (NTRKs) are a gene family function as oncogene or tumor suppressor gene in distinct cancers. We aimed to investigate the methylation and expression profiles and prognostic value of NTRKs gene in colorectal cancer (CRC). METHODS: An analysis of DNA methylation and expression profiles in CRC patients was performed to explore the critical methylations within NTRKs genes. The methylation marker was validated in a retrospectively collected cohort of 229 CRC patients and tested in other tumor types from TCGA. DNA methylation status was determined by quantitative methylation-specific PCR (QMSP). RESULTS: The profiles in six CRC cohorts showed that NTRKs gene promoter was more frequently methylated in CRC compared to normal mucosa, which was associated with suppressed gene expression. We identified a specific methylated region within NTRK3 promoter targeted by cg27034819 and cg11525479 that best predicted survival outcome in CRC. NTRK3 promoter methylation showed independently predictive value for survival outcome in the validation cohort (P = 0.004, HR 2.688, 95% CI [1.355, 5.333]). Based on this, a nomogram predicting survival outcome was developed with a C-index of 0.705. Furthermore, the addition of NTRK3 promoter methylation improved the performance of currently-used prognostic model (AIC: 516.49 vs 513.91; LR: 39.06 vs 43.64, P = 0.032). Finally, NTRK3 promoter methylation also predicted survival in other tumors, including pancreatic cancer, glioblastoma and stomach adenocarcinoma. CONCLUSIONS: This study highlights the essential value of NTRK3 methylation in prognostic evaluation and the potential to improve current prognostic models in CRC and other tumors.
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spelling pubmed-78852522021-02-17 Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer Chen, Zijian Huang, Zenghong Luo, Yanxin Zou, Qi Bai, Liangliang Tang, Guannan Wang, Xiaolin Cao, Guangwen Huang, Meijin Xiang, Jun Yu, Huichuan J Transl Med Research BACKGROUND: Neurotrophic tropomyosin receptor kinases (NTRKs) are a gene family function as oncogene or tumor suppressor gene in distinct cancers. We aimed to investigate the methylation and expression profiles and prognostic value of NTRKs gene in colorectal cancer (CRC). METHODS: An analysis of DNA methylation and expression profiles in CRC patients was performed to explore the critical methylations within NTRKs genes. The methylation marker was validated in a retrospectively collected cohort of 229 CRC patients and tested in other tumor types from TCGA. DNA methylation status was determined by quantitative methylation-specific PCR (QMSP). RESULTS: The profiles in six CRC cohorts showed that NTRKs gene promoter was more frequently methylated in CRC compared to normal mucosa, which was associated with suppressed gene expression. We identified a specific methylated region within NTRK3 promoter targeted by cg27034819 and cg11525479 that best predicted survival outcome in CRC. NTRK3 promoter methylation showed independently predictive value for survival outcome in the validation cohort (P = 0.004, HR 2.688, 95% CI [1.355, 5.333]). Based on this, a nomogram predicting survival outcome was developed with a C-index of 0.705. Furthermore, the addition of NTRK3 promoter methylation improved the performance of currently-used prognostic model (AIC: 516.49 vs 513.91; LR: 39.06 vs 43.64, P = 0.032). Finally, NTRK3 promoter methylation also predicted survival in other tumors, including pancreatic cancer, glioblastoma and stomach adenocarcinoma. CONCLUSIONS: This study highlights the essential value of NTRK3 methylation in prognostic evaluation and the potential to improve current prognostic models in CRC and other tumors. BioMed Central 2021-02-16 /pmc/articles/PMC7885252/ /pubmed/33593392 http://dx.doi.org/10.1186/s12967-021-02740-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Zijian
Huang, Zenghong
Luo, Yanxin
Zou, Qi
Bai, Liangliang
Tang, Guannan
Wang, Xiaolin
Cao, Guangwen
Huang, Meijin
Xiang, Jun
Yu, Huichuan
Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title_full Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title_fullStr Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title_full_unstemmed Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title_short Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer
title_sort genome-wide analysis identifies critical dna methylations within ntrks genes in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885252/
https://www.ncbi.nlm.nih.gov/pubmed/33593392
http://dx.doi.org/10.1186/s12967-021-02740-6
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