Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx

<p>Hepatocellular carcinoma (HCC) remains one of the leading causes of cancer-related mortality worldwide, characterized by increasing incidence rates and challenging prognoses. This study integrates single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics to unravel the complex mole...

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Main Author: Peng Zhu (277243) (author)
Other Authors: Lisha Mou (151003) (author), Ying Lu (66401) (author), Zuhui Pu (10931751) (author), Changchun Guo (12698009) (author)
Published: 2025
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_version_ 1852015420778741760
author Peng Zhu (277243)
author2 Lisha Mou (151003)
Ying Lu (66401)
Zuhui Pu (10931751)
Changchun Guo (12698009)
author2_role author
author
author
author
author_facet Peng Zhu (277243)
Lisha Mou (151003)
Ying Lu (66401)
Zuhui Pu (10931751)
Changchun Guo (12698009)
author_role author
dc.creator.none.fl_str_mv Peng Zhu (277243)
Lisha Mou (151003)
Ying Lu (66401)
Zuhui Pu (10931751)
Changchun Guo (12698009)
dc.date.none.fl_str_mv 2025-10-29T06:30:41Z
dc.identifier.none.fl_str_mv 10.3389/fimmu.2025.1680101.s010
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Table_7_Integrative_single-cell_and_spatial_transcriptomics_analysis_reveals_FLAD1_as_a_regulator_of_the_immune_microenvironment_in_hepatocellular_carcinoma_xlsx/30476348
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Genetic Immunology
hepatocellular carcinoma
mitochondrial function
single cell
spatial transcriptomics
machine learning
FLAD1
therapeutic targets
immune cell infiltration
dc.title.none.fl_str_mv Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <p>Hepatocellular carcinoma (HCC) remains one of the leading causes of cancer-related mortality worldwide, characterized by increasing incidence rates and challenging prognoses. This study integrates single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics to unravel the complex molecular and structural landscape of HCC, focusing on the identification of mitochondrial-related genes (MitRGs) and their pivotal role in disease progression. Utilizing scRNA-seq and bulk RNA-seq data, we performed a comprehensive differential expression analysis to highlight MitRGs. A modeling approach using 92 combinations of nine machine learning algorithms was applied, producing a predictive model with good performance. Among the genes analyzed, FLAD1 emerged as significantly upregulated in HCC tissues, correlating with advanced disease stages and poorer patient outcomes, and exhibited exceptional diagnostic accuracy with an AUC of 0.962. Functional enrichment analyses revealed that high FLAD1 expression is involved in crucial biological processes like copper ion detoxification and heme complex assembly. Interaction networks further elucidated the connection between FLAD1 and critical HCC pathways, with its expression levels negatively correlated with key immune effector cells such as CD8+ T cells and DCs. Spatial transcriptomics analysis provided a structural basis for this immune exclusion, demonstrating that an intact tumor capsule can function as a physical barrier that fosters an immune-exempt microenvironment. This analysis also validated FLAD1 upregulation within the spatial context of the tumor. Additionally, DNA methylation analysis indicated a hypomethylation pattern in the FLAD1 promoter region, likely contributing to its overexpression in HCC. Validation of FLAD1 protein levels in an in-house cohort via Western blotting further confirmed these findings. Collectively, our integrative study highlights the utility of MitRGs as potential biomarkers and positions FLAD1 as a dual prognostic and therapeutic target linked to the structural and immune landscape of HCC.</p>
eu_rights_str_mv openAccess
id Manara_7f28c0b0073e0be3c410ff6ef920d2d4
identifier_str_mv 10.3389/fimmu.2025.1680101.s010
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30476348
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsxPeng Zhu (277243)Lisha Mou (151003)Ying Lu (66401)Zuhui Pu (10931751)Changchun Guo (12698009)Genetic Immunologyhepatocellular carcinomamitochondrial functionsingle cellspatial transcriptomicsmachine learningFLAD1therapeutic targetsimmune cell infiltration<p>Hepatocellular carcinoma (HCC) remains one of the leading causes of cancer-related mortality worldwide, characterized by increasing incidence rates and challenging prognoses. This study integrates single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics to unravel the complex molecular and structural landscape of HCC, focusing on the identification of mitochondrial-related genes (MitRGs) and their pivotal role in disease progression. Utilizing scRNA-seq and bulk RNA-seq data, we performed a comprehensive differential expression analysis to highlight MitRGs. A modeling approach using 92 combinations of nine machine learning algorithms was applied, producing a predictive model with good performance. Among the genes analyzed, FLAD1 emerged as significantly upregulated in HCC tissues, correlating with advanced disease stages and poorer patient outcomes, and exhibited exceptional diagnostic accuracy with an AUC of 0.962. Functional enrichment analyses revealed that high FLAD1 expression is involved in crucial biological processes like copper ion detoxification and heme complex assembly. Interaction networks further elucidated the connection between FLAD1 and critical HCC pathways, with its expression levels negatively correlated with key immune effector cells such as CD8+ T cells and DCs. Spatial transcriptomics analysis provided a structural basis for this immune exclusion, demonstrating that an intact tumor capsule can function as a physical barrier that fosters an immune-exempt microenvironment. This analysis also validated FLAD1 upregulation within the spatial context of the tumor. Additionally, DNA methylation analysis indicated a hypomethylation pattern in the FLAD1 promoter region, likely contributing to its overexpression in HCC. Validation of FLAD1 protein levels in an in-house cohort via Western blotting further confirmed these findings. Collectively, our integrative study highlights the utility of MitRGs as potential biomarkers and positions FLAD1 as a dual prognostic and therapeutic target linked to the structural and immune landscape of HCC.</p>2025-10-29T06:30:41ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fimmu.2025.1680101.s010https://figshare.com/articles/dataset/Table_7_Integrative_single-cell_and_spatial_transcriptomics_analysis_reveals_FLAD1_as_a_regulator_of_the_immune_microenvironment_in_hepatocellular_carcinoma_xlsx/30476348CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/304763482025-10-29T06:30:41Z
spellingShingle Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
Peng Zhu (277243)
Genetic Immunology
hepatocellular carcinoma
mitochondrial function
single cell
spatial transcriptomics
machine learning
FLAD1
therapeutic targets
immune cell infiltration
status_str publishedVersion
title Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
title_full Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
title_fullStr Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
title_full_unstemmed Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
title_short Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
title_sort Table 7_Integrative single-cell and spatial transcriptomics analysis reveals FLAD1 as a regulator of the immune microenvironment in hepatocellular carcinoma.xlsx
topic Genetic Immunology
hepatocellular carcinoma
mitochondrial function
single cell
spatial transcriptomics
machine learning
FLAD1
therapeutic targets
immune cell infiltration