Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif

Background<p>Lung adenocarcinoma (LUAD) is a leading cause of cancer-related mortality. Protein succinylation, a key post-translational modification, is implicated in tumor progression. However, its comprehensive landscape and clinical significance in LUAD remain largely unexplored.</p>M...

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מחבר ראשי: Jichang Liu (1263291) (author)
מחברים אחרים: Xuehan Zhu (11957429) (author), Chenlong Zha (22687058) (author), Jiaqi Ding (8599578) (author), Chuanpeng Zhang (11677948) (author), Yizhe Wang (2287393) (author), Tao Yan (429415) (author), Hui Kong (4516105) (author), Yong Liu (6908) (author), Jingyu Chen (3571688) (author)
יצא לאור: 2025
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author Jichang Liu (1263291)
author2 Xuehan Zhu (11957429)
Chenlong Zha (22687058)
Jiaqi Ding (8599578)
Chuanpeng Zhang (11677948)
Yizhe Wang (2287393)
Tao Yan (429415)
Hui Kong (4516105)
Yong Liu (6908)
Jingyu Chen (3571688)
author2_role author
author
author
author
author
author
author
author
author
author_facet Jichang Liu (1263291)
Xuehan Zhu (11957429)
Chenlong Zha (22687058)
Jiaqi Ding (8599578)
Chuanpeng Zhang (11677948)
Yizhe Wang (2287393)
Tao Yan (429415)
Hui Kong (4516105)
Yong Liu (6908)
Jingyu Chen (3571688)
author_role author
dc.creator.none.fl_str_mv Jichang Liu (1263291)
Xuehan Zhu (11957429)
Chenlong Zha (22687058)
Jiaqi Ding (8599578)
Chuanpeng Zhang (11677948)
Yizhe Wang (2287393)
Tao Yan (429415)
Hui Kong (4516105)
Yong Liu (6908)
Jingyu Chen (3571688)
dc.date.none.fl_str_mv 2025-11-26T06:27:38Z
dc.identifier.none.fl_str_mv 10.3389/fimmu.2025.1718994.s012
dc.relation.none.fl_str_mv https://figshare.com/articles/figure/Image_3_Succinylation_heterogeneity_in_lung_adenocarcinoma_from_prognostic_model_to_KLK6-driven_tumor_microenvironment_remodeling_tif/30718373
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Genetic Immunology
succinylation
lung adenocarcinoma
KLK6
prognosis
immunotherapy
dc.title.none.fl_str_mv Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
dc.type.none.fl_str_mv Image
Figure
info:eu-repo/semantics/publishedVersion
image
description Background<p>Lung adenocarcinoma (LUAD) is a leading cause of cancer-related mortality. Protein succinylation, a key post-translational modification, is implicated in tumor progression. However, its comprehensive landscape and clinical significance in LUAD remain largely unexplored.</p>Methods<p>We integrated multi-omics data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) cohorts. A set of core succinylation-related genes was identified through differential expression and univariable Cox regression analyses. Molecular subtypes based on succinylation were determined by principal component analysis (PCA). A succinylation prognostic model was constructed via least absolute shrinkage and selection operator (LASSO) and multivariable Cox regression. The differences of tumor microenvironment (TME), tumor mutation burden and drug sensitivity in different risk groups were further explored. Single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics revealed effects of succinylation on TME. High-dimensional weighted gene co-expression networks analysis (hdWGCNA) was used to identify potential succinylation-related therapeutic targets. The function of therapeutic targets was further validated through scRNA-seq, spatial transcriptomics, and in vitro experiments.</p>Results<p>We identified 31 core succinylation-related genes and defined three molecular subtypes with distinct prognostic and TME characteristics. A robust 7-gene succinylation-based prognostic signature was developed and validated across 7 independent GEO cohorts, effectively stratifying patients into high- and low-risk groups with significant differences in survival, demonstrating high predictive accuracy, consistency, and clinical utility. The low-risk group exhibited an immunoreactive TME with enhanced immune cell infiltration and superior response to immunotherapy. scRNA-seq and spatial transcriptomics revealed enhanced succinylation in LUAD. Kallikrein-related peptidase 6 (KLK6) was identified as a potential therapeutic target. KLK6 was significantly upregulated in LUAD, correlated with poor prognosis and therapy resistance. KLK6 promoted global succinylation, proliferation, migration, and invasion of LUAD cells in vitro. Mechanistically, KLK6-positive tumor cells might foster an immunosuppressive TME by driving fibroblast-to-myofibroblast differentiation, enhancing extracellular matrix (ECM) deposition, and inhibiting CD8<sup>+</sup> T cell infiltration.</p>Conclusion<p>Our study delineates the succinylation landscape in LUAD, establishes a novel prognostic model for risk stratification and immunotherapy prediction. Meanwhile, we identified KLK6 as a potential promoter of tumor progression and immunosuppression. Targeting the succinylation pathway, particularly KLK6, may represent a promising therapeutic strategy for LUAD.</p>
eu_rights_str_mv openAccess
id Manara_67ad5fe5b48f1a41241be91516609e45
identifier_str_mv 10.3389/fimmu.2025.1718994.s012
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30718373
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tifJichang Liu (1263291)Xuehan Zhu (11957429)Chenlong Zha (22687058)Jiaqi Ding (8599578)Chuanpeng Zhang (11677948)Yizhe Wang (2287393)Tao Yan (429415)Hui Kong (4516105)Yong Liu (6908)Jingyu Chen (3571688)Genetic Immunologysuccinylationlung adenocarcinomaKLK6prognosisimmunotherapyBackground<p>Lung adenocarcinoma (LUAD) is a leading cause of cancer-related mortality. Protein succinylation, a key post-translational modification, is implicated in tumor progression. However, its comprehensive landscape and clinical significance in LUAD remain largely unexplored.</p>Methods<p>We integrated multi-omics data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) cohorts. A set of core succinylation-related genes was identified through differential expression and univariable Cox regression analyses. Molecular subtypes based on succinylation were determined by principal component analysis (PCA). A succinylation prognostic model was constructed via least absolute shrinkage and selection operator (LASSO) and multivariable Cox regression. The differences of tumor microenvironment (TME), tumor mutation burden and drug sensitivity in different risk groups were further explored. Single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics revealed effects of succinylation on TME. High-dimensional weighted gene co-expression networks analysis (hdWGCNA) was used to identify potential succinylation-related therapeutic targets. The function of therapeutic targets was further validated through scRNA-seq, spatial transcriptomics, and in vitro experiments.</p>Results<p>We identified 31 core succinylation-related genes and defined three molecular subtypes with distinct prognostic and TME characteristics. A robust 7-gene succinylation-based prognostic signature was developed and validated across 7 independent GEO cohorts, effectively stratifying patients into high- and low-risk groups with significant differences in survival, demonstrating high predictive accuracy, consistency, and clinical utility. The low-risk group exhibited an immunoreactive TME with enhanced immune cell infiltration and superior response to immunotherapy. scRNA-seq and spatial transcriptomics revealed enhanced succinylation in LUAD. Kallikrein-related peptidase 6 (KLK6) was identified as a potential therapeutic target. KLK6 was significantly upregulated in LUAD, correlated with poor prognosis and therapy resistance. KLK6 promoted global succinylation, proliferation, migration, and invasion of LUAD cells in vitro. Mechanistically, KLK6-positive tumor cells might foster an immunosuppressive TME by driving fibroblast-to-myofibroblast differentiation, enhancing extracellular matrix (ECM) deposition, and inhibiting CD8<sup>+</sup> T cell infiltration.</p>Conclusion<p>Our study delineates the succinylation landscape in LUAD, establishes a novel prognostic model for risk stratification and immunotherapy prediction. Meanwhile, we identified KLK6 as a potential promoter of tumor progression and immunosuppression. Targeting the succinylation pathway, particularly KLK6, may represent a promising therapeutic strategy for LUAD.</p>2025-11-26T06:27:38ZImageFigureinfo:eu-repo/semantics/publishedVersionimage10.3389/fimmu.2025.1718994.s012https://figshare.com/articles/figure/Image_3_Succinylation_heterogeneity_in_lung_adenocarcinoma_from_prognostic_model_to_KLK6-driven_tumor_microenvironment_remodeling_tif/30718373CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307183732025-11-26T06:27:38Z
spellingShingle Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
Jichang Liu (1263291)
Genetic Immunology
succinylation
lung adenocarcinoma
KLK6
prognosis
immunotherapy
status_str publishedVersion
title Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
title_full Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
title_fullStr Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
title_full_unstemmed Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
title_short Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
title_sort Image 3_Succinylation heterogeneity in lung adenocarcinoma: from prognostic model to KLK6-driven tumor microenvironment remodeling.tif
topic Genetic Immunology
succinylation
lung adenocarcinoma
KLK6
prognosis
immunotherapy