Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma

Abstract Background Sarcomas, cancers originating from mesenchymal cells, are comprehensive tumors with poor prognoses, yet their tumorigenic mechanisms are largely unknown. In this study, we characterize infiltrating immune cells and analyze immune scores to identify the molecular mechanism of immu...

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Main Authors: Naiqiang Zhu, Jingyi Hou
格式: Article
語言:English
出版: BMC 2020-12-01
叢編:Cancer Cell International
主題:
在線閱讀:https://doi.org/10.1186/s12935-020-01672-3
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author Naiqiang Zhu
Jingyi Hou
author_facet Naiqiang Zhu
Jingyi Hou
author_sort Naiqiang Zhu
collection DOAJ
description Abstract Background Sarcomas, cancers originating from mesenchymal cells, are comprehensive tumors with poor prognoses, yet their tumorigenic mechanisms are largely unknown. In this study, we characterize infiltrating immune cells and analyze immune scores to identify the molecular mechanism of immunologic response to sarcomas. Method The “CIBERSORT” algorithm was used to calculate the amount of L22 immune cell infiltration in sarcomas. Then, the “ESTIMATE” algorithm was used to assess the “Estimate,” “Immune,” and “Stromal” scores. Weighted gene co-expression network analysis (WGCNA) was utilized to identify the significant module related to the immune therapeutic target. Gene ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed using the “clusterProfiler” package in R for annotation and visualization. Results Macrophages were the most common immune cells infiltrating sarcomas. The number of CD8 T cells was negatively associated with that of M0 and M2 macrophages, and positively associated with M macrophages in sarcomas samples. The clinical parameters (disease type, gender) significantly increased with higher Estimate, Immune, and Stromal scores, and with a better prognosis. The blue module was significantly associated with CD8 T cells. Functional enrichment analysis showed that the blue module was mainly involved in chemokine signaling and the PI3K-Akt signaling pathway. CD48, P2RY10 and RASAL3 were identified and validated at the protein level. Conclusion Based on the immune cell infiltration and immune microenvironment, three key genes were identified, thus presenting novel molecular mechanisms of sarcoma metastasis.
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spelling doaj.art-acc4b57af1a842f6a61a2fef88093b512022-12-21T20:30:11ZengBMCCancer Cell International1475-28672020-12-0120111110.1186/s12935-020-01672-3Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcomaNaiqiang Zhu0Jingyi Hou1Department of Minimally Invasive Spinal Surgery, Affiliated Hospital of Chengde Medical CollegeDepartment of Minimally Invasive Spinal Surgery, Affiliated Hospital of Chengde Medical CollegeAbstract Background Sarcomas, cancers originating from mesenchymal cells, are comprehensive tumors with poor prognoses, yet their tumorigenic mechanisms are largely unknown. In this study, we characterize infiltrating immune cells and analyze immune scores to identify the molecular mechanism of immunologic response to sarcomas. Method The “CIBERSORT” algorithm was used to calculate the amount of L22 immune cell infiltration in sarcomas. Then, the “ESTIMATE” algorithm was used to assess the “Estimate,” “Immune,” and “Stromal” scores. Weighted gene co-expression network analysis (WGCNA) was utilized to identify the significant module related to the immune therapeutic target. Gene ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed using the “clusterProfiler” package in R for annotation and visualization. Results Macrophages were the most common immune cells infiltrating sarcomas. The number of CD8 T cells was negatively associated with that of M0 and M2 macrophages, and positively associated with M macrophages in sarcomas samples. The clinical parameters (disease type, gender) significantly increased with higher Estimate, Immune, and Stromal scores, and with a better prognosis. The blue module was significantly associated with CD8 T cells. Functional enrichment analysis showed that the blue module was mainly involved in chemokine signaling and the PI3K-Akt signaling pathway. CD48, P2RY10 and RASAL3 were identified and validated at the protein level. Conclusion Based on the immune cell infiltration and immune microenvironment, three key genes were identified, thus presenting novel molecular mechanisms of sarcoma metastasis.https://doi.org/10.1186/s12935-020-01672-3SarcomasImmune infiltrationPrognosisWeighted gene co-expression analysisTumor microenvironment
spellingShingle Naiqiang Zhu
Jingyi Hou
Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
Cancer Cell International
Sarcomas
Immune infiltration
Prognosis
Weighted gene co-expression analysis
Tumor microenvironment
title Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
title_full Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
title_fullStr Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
title_full_unstemmed Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
title_short Assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
title_sort assessing immune infiltration and the tumor microenvironment for the diagnosis and prognosis of sarcoma
topic Sarcomas
Immune infiltration
Prognosis
Weighted gene co-expression analysis
Tumor microenvironment
url https://doi.org/10.1186/s12935-020-01672-3
work_keys_str_mv AT naiqiangzhu assessingimmuneinfiltrationandthetumormicroenvironmentforthediagnosisandprognosisofsarcoma
AT jingyihou assessingimmuneinfiltrationandthetumormicroenvironmentforthediagnosisandprognosisofsarcoma