Cargando…
Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma
BACKGROUND: MYCN amplification and age are two critical prognostic factors of pediatric neuroblastoma. Previously, we had revealed the prognosis of MYCN target genes. However, the prognostic effects of age related genes in neuroblastoma are unclear. METHODS: The prognostic significance of age and MY...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194129/ https://www.ncbi.nlm.nih.gov/pubmed/34116676 http://dx.doi.org/10.1186/s12887-021-02753-6 |
_version_ | 1783706356775124992 |
---|---|
author | Wang, Haiwei Wang, Xinrui Xu, Liangpu Zhang, Ji Cao, Hua |
author_facet | Wang, Haiwei Wang, Xinrui Xu, Liangpu Zhang, Ji Cao, Hua |
author_sort | Wang, Haiwei |
collection | PubMed |
description | BACKGROUND: MYCN amplification and age are two critical prognostic factors of pediatric neuroblastoma. Previously, we had revealed the prognosis of MYCN target genes. However, the prognostic effects of age related genes in neuroblastoma are unclear. METHODS: The prognostic significance of age and MYCN amplification was determined through multivariate cox regression and Kaplan-Meier survival analysis. Genes differentially expressed in MYCN non-amplified younger neuroblastoma patients were identified using Therapeutically Applicable Research to Generate Effective Treatments (TARGET) and Gene Expression Omnibus (GEO) datasets. The prognostic effects of age related genes ALCAM, CACNA2D3, DST, EPB41L4A and KIF1B in pediatric neuroblastoma patients were determined by Kaplan-Meier survival. RESULTS: In a pediatric pan-cancer analysis, age was associated with the overall survival of pediatric B-lineage acute lymphoblastic leukemia, neuroblastoma and wilms tumor in TARGET dataset. Moreover, the prognostic effects of age in neuroblastoma were validated using two independent neuroblastoma cohorts. Furthermore, age and MYCN amplification were independent prognostic factors in pediatric neuroblastoma. Compared with MYCN non-amplified older neuroblastoma patients, MYCN non-amplified younger neuroblastoma patients had better clinical outcomes. ALCAM, CACNA2D3, DST, EPB41L4A and KIF1B were highly expressed in MYCN non-amplified younger neuroblastoma patients. And the higher expression levels of ALCAM, CACNA2D3, DST, EPB41L4A or KIF1B were associated with better prognosis of MYCN non-amplified neuroblastoma patients. DST was an independent prognostic factor in MYCN non-amplified neuroblastoma patients and MYCN non-amplified neuroblastoma younger patients with higher DST expression levels had the best clinical overall survival. CONCLUSIONS: Age related gene DST was an independent prognostic factor in MYCN non-amplified neuroblastoma. MYCN non-amplified younger neuroblastoma patients with higher DST expression levels had the best clinical overall survival. |
format | Online Article Text |
id | pubmed-8194129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81941292021-06-15 Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma Wang, Haiwei Wang, Xinrui Xu, Liangpu Zhang, Ji Cao, Hua BMC Pediatr Research BACKGROUND: MYCN amplification and age are two critical prognostic factors of pediatric neuroblastoma. Previously, we had revealed the prognosis of MYCN target genes. However, the prognostic effects of age related genes in neuroblastoma are unclear. METHODS: The prognostic significance of age and MYCN amplification was determined through multivariate cox regression and Kaplan-Meier survival analysis. Genes differentially expressed in MYCN non-amplified younger neuroblastoma patients were identified using Therapeutically Applicable Research to Generate Effective Treatments (TARGET) and Gene Expression Omnibus (GEO) datasets. The prognostic effects of age related genes ALCAM, CACNA2D3, DST, EPB41L4A and KIF1B in pediatric neuroblastoma patients were determined by Kaplan-Meier survival. RESULTS: In a pediatric pan-cancer analysis, age was associated with the overall survival of pediatric B-lineage acute lymphoblastic leukemia, neuroblastoma and wilms tumor in TARGET dataset. Moreover, the prognostic effects of age in neuroblastoma were validated using two independent neuroblastoma cohorts. Furthermore, age and MYCN amplification were independent prognostic factors in pediatric neuroblastoma. Compared with MYCN non-amplified older neuroblastoma patients, MYCN non-amplified younger neuroblastoma patients had better clinical outcomes. ALCAM, CACNA2D3, DST, EPB41L4A and KIF1B were highly expressed in MYCN non-amplified younger neuroblastoma patients. And the higher expression levels of ALCAM, CACNA2D3, DST, EPB41L4A or KIF1B were associated with better prognosis of MYCN non-amplified neuroblastoma patients. DST was an independent prognostic factor in MYCN non-amplified neuroblastoma patients and MYCN non-amplified neuroblastoma younger patients with higher DST expression levels had the best clinical overall survival. CONCLUSIONS: Age related gene DST was an independent prognostic factor in MYCN non-amplified neuroblastoma. MYCN non-amplified younger neuroblastoma patients with higher DST expression levels had the best clinical overall survival. BioMed Central 2021-06-11 /pmc/articles/PMC8194129/ /pubmed/34116676 http://dx.doi.org/10.1186/s12887-021-02753-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Wang, Haiwei Wang, Xinrui Xu, Liangpu Zhang, Ji Cao, Hua Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title | Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title_full | Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title_fullStr | Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title_full_unstemmed | Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title_short | Age related gene DST represents an independent prognostic factor for MYCN non-amplified neuroblastoma |
title_sort | age related gene dst represents an independent prognostic factor for mycn non-amplified neuroblastoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194129/ https://www.ncbi.nlm.nih.gov/pubmed/34116676 http://dx.doi.org/10.1186/s12887-021-02753-6 |
work_keys_str_mv | AT wanghaiwei agerelatedgenedstrepresentsanindependentprognosticfactorformycnnonamplifiedneuroblastoma AT wangxinrui agerelatedgenedstrepresentsanindependentprognosticfactorformycnnonamplifiedneuroblastoma AT xuliangpu agerelatedgenedstrepresentsanindependentprognosticfactorformycnnonamplifiedneuroblastoma AT zhangji agerelatedgenedstrepresentsanindependentprognosticfactorformycnnonamplifiedneuroblastoma AT caohua agerelatedgenedstrepresentsanindependentprognosticfactorformycnnonamplifiedneuroblastoma |