Cargando…

Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer

BACKGROUND: The origin recognition complex 1 (ORC1) is a large subunit of the origin recognition complex and acts as the master subunit of the precoding complex. OBJECTIVE: To explore potential function and clinical significance of ORC1 in cancers. METHODS: The expression level of ORC1 in different...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Linling, Chen, Hui, Yang, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571394/
https://www.ncbi.nlm.nih.gov/pubmed/37833711
http://dx.doi.org/10.1186/s12920-023-01691-9
_version_ 1785119988398424064
author Wu, Linling
Chen, Hui
Yang, Chao
author_facet Wu, Linling
Chen, Hui
Yang, Chao
author_sort Wu, Linling
collection PubMed
description BACKGROUND: The origin recognition complex 1 (ORC1) is a large subunit of the origin recognition complex and acts as the master subunit of the precoding complex. OBJECTIVE: To explore potential function and clinical significance of ORC1 in cancers. METHODS: The expression level of ORC1 in different types of tumor tissues and matched normal tissues were detected by The Cancer Genome Atlas (TCGA) and validated by datasets from the gene expression omnibus (GEO) database. The association between ORC1 expression and infiltration levels of immune cell was analyzed. ORC1 and its co-expression genes were subjected to enrichment analysis to explore potential mechanisms in cancers, and the protein-protein interaction (PPI) network was constructed. Finally, the expression of ORC1 in tumor tissue and adjacent tissue was verified by immunohistochemistry (IHC). RESULTS: ORC1 was highly expressed in the majority of tumors, and the expression level of ORC1 was associated with the pathological stages of ACC, LUAD, OV and SKCM. ORC1 was closely related with poor prognosis in ACC, LIHC, PAAD, READ and THCA. ORC1 in ACC and KICH was positively correlated with the infiltration level of immune cells while it was negatively correlated with the infiltration level of immune cells in THYM. Co-expression network analysis showed that CDCA3, GSG2, KIF2C, NCAPH and PLK1 were positively correlated with ORC1 in cancer, and enrichment analysis showed a correlation with cytosol, ATP binding and cell division. The expression of ORC1 in UCEC and KICH was higher than that in the adjacent tissues. CONCLUSION: ORC1 over-expressed in most tumors and could be severed as a novel biomarker for diagnosis. This study revealed that ORC1 might inhibit tumor immunity and might be a potential therapeutic target in cancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01691-9.
format Online
Article
Text
id pubmed-10571394
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-105713942023-10-14 Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer Wu, Linling Chen, Hui Yang, Chao BMC Med Genomics Research BACKGROUND: The origin recognition complex 1 (ORC1) is a large subunit of the origin recognition complex and acts as the master subunit of the precoding complex. OBJECTIVE: To explore potential function and clinical significance of ORC1 in cancers. METHODS: The expression level of ORC1 in different types of tumor tissues and matched normal tissues were detected by The Cancer Genome Atlas (TCGA) and validated by datasets from the gene expression omnibus (GEO) database. The association between ORC1 expression and infiltration levels of immune cell was analyzed. ORC1 and its co-expression genes were subjected to enrichment analysis to explore potential mechanisms in cancers, and the protein-protein interaction (PPI) network was constructed. Finally, the expression of ORC1 in tumor tissue and adjacent tissue was verified by immunohistochemistry (IHC). RESULTS: ORC1 was highly expressed in the majority of tumors, and the expression level of ORC1 was associated with the pathological stages of ACC, LUAD, OV and SKCM. ORC1 was closely related with poor prognosis in ACC, LIHC, PAAD, READ and THCA. ORC1 in ACC and KICH was positively correlated with the infiltration level of immune cells while it was negatively correlated with the infiltration level of immune cells in THYM. Co-expression network analysis showed that CDCA3, GSG2, KIF2C, NCAPH and PLK1 were positively correlated with ORC1 in cancer, and enrichment analysis showed a correlation with cytosol, ATP binding and cell division. The expression of ORC1 in UCEC and KICH was higher than that in the adjacent tissues. CONCLUSION: ORC1 over-expressed in most tumors and could be severed as a novel biomarker for diagnosis. This study revealed that ORC1 might inhibit tumor immunity and might be a potential therapeutic target in cancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01691-9. BioMed Central 2023-10-13 /pmc/articles/PMC10571394/ /pubmed/37833711 http://dx.doi.org/10.1186/s12920-023-01691-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Wu, Linling
Chen, Hui
Yang, Chao
Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title_full Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title_fullStr Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title_full_unstemmed Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title_short Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancer
title_sort origin recognition complex subunit 1(orc1) is a potential biomarker and therapeutic target in cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571394/
https://www.ncbi.nlm.nih.gov/pubmed/37833711
http://dx.doi.org/10.1186/s12920-023-01691-9
work_keys_str_mv AT wulinling originrecognitioncomplexsubunit1orc1isapotentialbiomarkerandtherapeutictargetincancer
AT chenhui originrecognitioncomplexsubunit1orc1isapotentialbiomarkerandtherapeutictargetincancer
AT yangchao originrecognitioncomplexsubunit1orc1isapotentialbiomarkerandtherapeutictargetincancer