Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database

Abstract Background In terms of biological behavior, gene regulation, or signaling pathways, there is a certain similarity between tumorigenesis and embryonic development of humans. Three germ layer structure exhibits the distinct ability to form specific tissues and organs. Methods The present stud...

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Main Authors: Xingjie Gao, Xiaoteng Cui, Xinxin Zhang, Chunyan Zhao, Nan Zhang, Yan Zhao, Yuanyuan Ren, Chao Su, Lin Ge, Shaoyuan Wu, Jie Yang
Format: Article
Language:English
Published: BMC 2020-12-01
Series:Cancer Cell International
Subjects:
Online Access:https://doi.org/10.1186/s12935-020-01678-x
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spelling doaj-d1e6d7e7521641b5ac2f6f265c128f5d2020-12-13T12:16:58ZengBMCCancer Cell International1475-28672020-12-0120111410.1186/s12935-020-01678-xDifferential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA databaseXingjie Gao0Xiaoteng Cui1Xinxin Zhang2Chunyan Zhao3Nan Zhang4Yan Zhao5Yuanyuan Ren6Chao Su7Lin Ge8Shaoyuan Wu9Jie Yang10Department of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityDepartment of Biochemistry and Molecular Biology, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical UniversityAbstract Background In terms of biological behavior, gene regulation, or signaling pathways, there is a certain similarity between tumorigenesis and embryonic development of humans. Three germ layer structure exhibits the distinct ability to form specific tissues and organs. Methods The present study set out to investigate the genetic mutation characteristics of germ layer differentiation-related genes using the tumor cases of the cancer genome atlas (TCGA) database. Results These tumor samples were divided into three groups, including the ectoderm, mesoderm, and endoderm. Children cases less than 9 years old accounted for a larger proportion for the cases in the ectoderm and mesoderm groups; whereas the middle-aged and elderly individuals (from 50 to 89 years old) were more susceptible to tumors of endoderm. There was a better prognosis for the cases of mesoderm, especially the male with the race of White, compared with the other groups. A missense mutation was frequently detected for the cases of ectoderm and endoderm, while deletion mutation was common for that of mesoderm. We could not identify the ectoderm, mesoderm, or endoderm-specific mutated genes or variants with high mutation frequency. However, there was a relatively higher mutation incidence of endoderm markers (GATA6, FOXA2, GATA4, AFP) in the endoderm group, compared with the groups of ectoderm and mesoderm. Additionally, four members (SMO, GLI1, GLI2, GLI3) within the Hedgehog signaling pathway genes showed a relatively higher mutation rate in the endoderm group than the other two groups. Conclusions TCGA tumors of ectoderm, mesoderm, and endoderm groups exhibit the distinct subject distribution, survival status, and genomic alteration characteristics. The synergistic mutation effect of specific genes closely related to embryonic development may contribute to the tumorigenesis of tissues or organs derived from the specific germ layers. This study provides a novel reference for exploring the functional connection between embryogenesis and tumorigenesis.https://doi.org/10.1186/s12935-020-01678-xEctodermMesodermEndodermTumorTCGAGenetic mutation
collection DOAJ
language English
format Article
sources DOAJ
author Xingjie Gao
Xiaoteng Cui
Xinxin Zhang
Chunyan Zhao
Nan Zhang
Yan Zhao
Yuanyuan Ren
Chao Su
Lin Ge
Shaoyuan Wu
Jie Yang
spellingShingle Xingjie Gao
Xiaoteng Cui
Xinxin Zhang
Chunyan Zhao
Nan Zhang
Yan Zhao
Yuanyuan Ren
Chao Su
Lin Ge
Shaoyuan Wu
Jie Yang
Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
Cancer Cell International
Ectoderm
Mesoderm
Endoderm
Tumor
TCGA
Genetic mutation
author_facet Xingjie Gao
Xiaoteng Cui
Xinxin Zhang
Chunyan Zhao
Nan Zhang
Yan Zhao
Yuanyuan Ren
Chao Su
Lin Ge
Shaoyuan Wu
Jie Yang
author_sort Xingjie Gao
title Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
title_short Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
title_full Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
title_fullStr Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
title_full_unstemmed Differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in TCGA database
title_sort differential genetic mutations of ectoderm, mesoderm, and endoderm-derived tumors in tcga database
publisher BMC
series Cancer Cell International
issn 1475-2867
publishDate 2020-12-01
description Abstract Background In terms of biological behavior, gene regulation, or signaling pathways, there is a certain similarity between tumorigenesis and embryonic development of humans. Three germ layer structure exhibits the distinct ability to form specific tissues and organs. Methods The present study set out to investigate the genetic mutation characteristics of germ layer differentiation-related genes using the tumor cases of the cancer genome atlas (TCGA) database. Results These tumor samples were divided into three groups, including the ectoderm, mesoderm, and endoderm. Children cases less than 9 years old accounted for a larger proportion for the cases in the ectoderm and mesoderm groups; whereas the middle-aged and elderly individuals (from 50 to 89 years old) were more susceptible to tumors of endoderm. There was a better prognosis for the cases of mesoderm, especially the male with the race of White, compared with the other groups. A missense mutation was frequently detected for the cases of ectoderm and endoderm, while deletion mutation was common for that of mesoderm. We could not identify the ectoderm, mesoderm, or endoderm-specific mutated genes or variants with high mutation frequency. However, there was a relatively higher mutation incidence of endoderm markers (GATA6, FOXA2, GATA4, AFP) in the endoderm group, compared with the groups of ectoderm and mesoderm. Additionally, four members (SMO, GLI1, GLI2, GLI3) within the Hedgehog signaling pathway genes showed a relatively higher mutation rate in the endoderm group than the other two groups. Conclusions TCGA tumors of ectoderm, mesoderm, and endoderm groups exhibit the distinct subject distribution, survival status, and genomic alteration characteristics. The synergistic mutation effect of specific genes closely related to embryonic development may contribute to the tumorigenesis of tissues or organs derived from the specific germ layers. This study provides a novel reference for exploring the functional connection between embryogenesis and tumorigenesis.
topic Ectoderm
Mesoderm
Endoderm
Tumor
TCGA
Genetic mutation
url https://doi.org/10.1186/s12935-020-01678-x
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