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Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses
BACKGROUND: Armadillo repeat-containing 10 (ARMC10) is involved in the progression of multiple types of tumors. Pancreatic adenocarcinoma (PAAD) is a lethal disease with poor survival and prognosis. METHODS: We acquired the data of ARMC10 in PAAD patients from the cancer genome atlas (TCGA) and gene...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569960/ https://www.ncbi.nlm.nih.gov/pubmed/37842592 http://dx.doi.org/10.1016/j.heliyon.2023.e20464 |
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author | Li, Tian-Hao Qin, Xiao-Han Wang, Li-Quan Qin, Cheng Zhao, Bang-Bo Cao, Hong-Tao Yang, Xiao-Ying Wang, Yuan-Yang Li, Ze-Ru Zhou, Xing-Tong Wang, Wei-Bin |
author_facet | Li, Tian-Hao Qin, Xiao-Han Wang, Li-Quan Qin, Cheng Zhao, Bang-Bo Cao, Hong-Tao Yang, Xiao-Ying Wang, Yuan-Yang Li, Ze-Ru Zhou, Xing-Tong Wang, Wei-Bin |
author_sort | Li, Tian-Hao |
collection | PubMed |
description | BACKGROUND: Armadillo repeat-containing 10 (ARMC10) is involved in the progression of multiple types of tumors. Pancreatic adenocarcinoma (PAAD) is a lethal disease with poor survival and prognosis. METHODS: We acquired the data of ARMC10 in PAAD patients from the cancer genome atlas (TCGA) and gene expression omnibus (GEO) datasets and compared the expression level with normal pancreatic tissues. We evaluated the relevance between ARMC10 expression and clinicopathological factors, immune infiltration degree and prognosis in PAAD. RESULTS: High expression of ARMC10 was relevant to T stage, M stage, pathologic stage, histologic grade, residual tumor, primary therapy outcome (P < 0.05) and related to lower Overall-Survival (OS), Disease-Specific Survival (DSS), and Progression-Free Interval (PFI). Gene set enrichment analysis showed that ARMC10 was related to methylation in neural precursor cells (NPC), G alpha (i) signaling events, APC targets, energy metabolism, potassium channels and IL10 synthesis. The expression level of ARMC10 was positively related to the abundance of T helper cells and negatively to that of plasmacytoid dendritic cells (pDCs). Knocking down of ARMC10 could lead to lower proliferation, invasion, migration ability and colony formation rate of PAAD cells in vitro. CONCLUSIONS: Our research firstly discovered ARMC10 as a novel prognostic biomarker for PAAD patients and played a crucial role in immune regulation in PAAD. |
format | Online Article Text |
id | pubmed-10569960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105699602023-10-14 Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses Li, Tian-Hao Qin, Xiao-Han Wang, Li-Quan Qin, Cheng Zhao, Bang-Bo Cao, Hong-Tao Yang, Xiao-Ying Wang, Yuan-Yang Li, Ze-Ru Zhou, Xing-Tong Wang, Wei-Bin Heliyon Research Article BACKGROUND: Armadillo repeat-containing 10 (ARMC10) is involved in the progression of multiple types of tumors. Pancreatic adenocarcinoma (PAAD) is a lethal disease with poor survival and prognosis. METHODS: We acquired the data of ARMC10 in PAAD patients from the cancer genome atlas (TCGA) and gene expression omnibus (GEO) datasets and compared the expression level with normal pancreatic tissues. We evaluated the relevance between ARMC10 expression and clinicopathological factors, immune infiltration degree and prognosis in PAAD. RESULTS: High expression of ARMC10 was relevant to T stage, M stage, pathologic stage, histologic grade, residual tumor, primary therapy outcome (P < 0.05) and related to lower Overall-Survival (OS), Disease-Specific Survival (DSS), and Progression-Free Interval (PFI). Gene set enrichment analysis showed that ARMC10 was related to methylation in neural precursor cells (NPC), G alpha (i) signaling events, APC targets, energy metabolism, potassium channels and IL10 synthesis. The expression level of ARMC10 was positively related to the abundance of T helper cells and negatively to that of plasmacytoid dendritic cells (pDCs). Knocking down of ARMC10 could lead to lower proliferation, invasion, migration ability and colony formation rate of PAAD cells in vitro. CONCLUSIONS: Our research firstly discovered ARMC10 as a novel prognostic biomarker for PAAD patients and played a crucial role in immune regulation in PAAD. Elsevier 2023-09-27 /pmc/articles/PMC10569960/ /pubmed/37842592 http://dx.doi.org/10.1016/j.heliyon.2023.e20464 Text en © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Li, Tian-Hao Qin, Xiao-Han Wang, Li-Quan Qin, Cheng Zhao, Bang-Bo Cao, Hong-Tao Yang, Xiao-Ying Wang, Yuan-Yang Li, Ze-Ru Zhou, Xing-Tong Wang, Wei-Bin Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title | Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title_full | Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title_fullStr | Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title_full_unstemmed | Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title_short | Prognostic value and immune infiltration of ARMC10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
title_sort | prognostic value and immune infiltration of armc10 in pancreatic adenocarcinoma via integrated bioinformatics analyses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569960/ https://www.ncbi.nlm.nih.gov/pubmed/37842592 http://dx.doi.org/10.1016/j.heliyon.2023.e20464 |
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