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BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide, and its pathophysiological mechanisms remain unknown. IRSp53 family members, such as BAIAP2L1, participate in the progression of multiple tumors. However, the role of BAIAP2L2 in HCC remains unclear. This study comp...

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Autores principales: Wei, Hui, Yang, Jing, Chen, Xia, Liu, Mengxiao, Zhang, Huiyun, Sun, Weiming, Wang, Yuping, Zhou, Yongning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227027/
https://www.ncbi.nlm.nih.gov/pubmed/37248248
http://dx.doi.org/10.1038/s41598-023-35420-0
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author Wei, Hui
Yang, Jing
Chen, Xia
Liu, Mengxiao
Zhang, Huiyun
Sun, Weiming
Wang, Yuping
Zhou, Yongning
author_facet Wei, Hui
Yang, Jing
Chen, Xia
Liu, Mengxiao
Zhang, Huiyun
Sun, Weiming
Wang, Yuping
Zhou, Yongning
author_sort Wei, Hui
collection PubMed
description Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide, and its pathophysiological mechanisms remain unknown. IRSp53 family members, such as BAIAP2L1, participate in the progression of multiple tumors. However, the role of BAIAP2L2 in HCC remains unclear. This study comprehensively analyzed the potential role of BAIAP2L2 in HCC using bioinformatic techniques. The expression of BAIAP2L2 in HCC was analyzed using The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), International Cancer Genome Consortium (ICGC), and Human Protein Atlas (HPA) databases and in vitro experiments. In addition, the prognostic value of BAIAP2L2 in HCC was analyzed using the TCGA database. TCGA and GEO database were used to analyze the role of BAIAP2L2 in immune features. We also explored the function of BAIAP2L2 in methylation and cuprotosis. The CellMiner database was used to analyze the relationship between BAIAP2L2 expression and drug sensitivity. Our study revealed that BAIAP2L2 is overexpressed in HCC and promotes the migration and invasion of HCC cells. BAIAP2L2 may affect the prognosis of HCC by regulating immunity, methylation, and cuprotosis. BAIAP2L2 is a novel HCC prognostic gene involved in immune infiltration associated with cuprotosis and may be a potential prognosis and therapeutic target for HCC.
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spelling pubmed-102270272023-05-31 BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis Wei, Hui Yang, Jing Chen, Xia Liu, Mengxiao Zhang, Huiyun Sun, Weiming Wang, Yuping Zhou, Yongning Sci Rep Article Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide, and its pathophysiological mechanisms remain unknown. IRSp53 family members, such as BAIAP2L1, participate in the progression of multiple tumors. However, the role of BAIAP2L2 in HCC remains unclear. This study comprehensively analyzed the potential role of BAIAP2L2 in HCC using bioinformatic techniques. The expression of BAIAP2L2 in HCC was analyzed using The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), International Cancer Genome Consortium (ICGC), and Human Protein Atlas (HPA) databases and in vitro experiments. In addition, the prognostic value of BAIAP2L2 in HCC was analyzed using the TCGA database. TCGA and GEO database were used to analyze the role of BAIAP2L2 in immune features. We also explored the function of BAIAP2L2 in methylation and cuprotosis. The CellMiner database was used to analyze the relationship between BAIAP2L2 expression and drug sensitivity. Our study revealed that BAIAP2L2 is overexpressed in HCC and promotes the migration and invasion of HCC cells. BAIAP2L2 may affect the prognosis of HCC by regulating immunity, methylation, and cuprotosis. BAIAP2L2 is a novel HCC prognostic gene involved in immune infiltration associated with cuprotosis and may be a potential prognosis and therapeutic target for HCC. Nature Publishing Group UK 2023-05-29 /pmc/articles/PMC10227027/ /pubmed/37248248 http://dx.doi.org/10.1038/s41598-023-35420-0 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/) .
spellingShingle Article
Wei, Hui
Yang, Jing
Chen, Xia
Liu, Mengxiao
Zhang, Huiyun
Sun, Weiming
Wang, Yuping
Zhou, Yongning
BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title_full BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title_fullStr BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title_full_unstemmed BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title_short BAIAP2L2 is a novel prognostic biomarker related to migration and invasion of HCC and associated with cuprotosis
title_sort baiap2l2 is a novel prognostic biomarker related to migration and invasion of hcc and associated with cuprotosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227027/
https://www.ncbi.nlm.nih.gov/pubmed/37248248
http://dx.doi.org/10.1038/s41598-023-35420-0
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