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pmid:37100454

Development and validation of novel prognostic models for zinc finger proteins-related genes in soft tissue sarcoma.

Junqing Li · Quan Zhou · Changsheng Zhang · Huimin Zhu · Jie Yao · Meng Zhang

Aging · 2023 doi:10.18632/aging.204682

Paper

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Experiment

complete

Data

partial

Analysis

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title
Development and validation of novel prognostic models for zinc finger proteins-related genes in soft tissue sarcoma.
doi
10.18632/aging.204682
pmid
37100454
authors array · 6 items
[0]
Junqing Li
[1]
Quan Zhou
[2]
Changsheng Zhang
[3]
Huimin Zhu
[4]
Jie Yao
[5]
Meng Zhang
journal
Aging
year
2023
abstract
As the most common transcriptional regulators, zinc finer proteins (ZNFs) play vital roles in occurrence and progression of malignant tumors. Whereas, information regarding the roles of ZNFs in soft tissue sarcomas (STS) remains scarce. In this study, a comprehensive bioinformatics analysis investigating roles of ZNFs in STS was performed. Initially, we extracted raw datasets of differentially expressed ZNFs from GSE2719. Using a sequence of bioinformatics methods, we then investigated the prognostic significance, function, and molecular subtype of these differentially expressed ZNFs. In addition, CCK8 and plate clone formation assays were used to explore the effect of ZNF141 on STS cells. A total of 110 differentially expressed ZNFs were identified. Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model. Compared with patients with low-risk in the TCGA training and testing cohorts, as well as the GEO validation cohorts, patients with high-risk had poorer OS and PFS. Using nomograms constructed with the identified ZNFs predicting OS and PFS, we established a clinically useful model. Four distinct molecular subtypes with different prognostic and immune infiltration characteristics were identified. In vitro experiments showed that ZNF141 promoted the proliferation and viability of STS cells. In conclusion, ZNF-related models are useful as prognostic biomarkers, suggesting their potentials as therapeutic targets in STS. These findings will enable us to develop novel strategies treating STS, which will potentially improve outcomes of patients with STS.
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Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models.
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Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models.
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All datasets presented in this study are included in the article/Supplementary Material.
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Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model.
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Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model.
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Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model.
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GSM766583
[51]
GSM766584
[52]
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[53]
GSM766586
[54]
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[55]
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[56]
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[58]
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[59]
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[61]
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[62]
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[63]
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[64]
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[65]
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[66]
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[67]
GSM766600
[68]
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[69]
GSM766602
[70]
GSM766603
[71]
GSM766604
[72]
GSM766605
[73]
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[74]
GSM766607
[75]
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[76]
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[77]
GSM766610
[78]
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[79]
GSM766612
[80]
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[81]
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[82]
GSM766615
[83]
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[84]
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[85]
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[86]
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[87]
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[88]
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[89]
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[90]
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[91]
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[92]
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[93]
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[94]
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[95]
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[96]
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[97]
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[98]
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[99]
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[100]
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[101]
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[102]
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[103]
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[104]
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[105]
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[106]
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[107]
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[108]
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[109]
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[110]
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[111]
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[112]
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[113]
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[114]
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[115]
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[116]
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[117]
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[118]
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[119]
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[120]
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[121]
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[122]
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[123]
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[124]
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[125]
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[126]
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[127]
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[128]
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[129]
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[130]
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[131]
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[132]
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[133]
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[134]
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[135]
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[136]
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[137]
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[138]
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[139]
GSM766672
sample_count
140
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
Whole-transcript expression data for liposarcoma
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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[0]
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[1]
asset:data:geo:GSE21050 licence not read
[2]
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[3]
asset:data:geo:GSE2719 licence not read
[4]
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[5]
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method-1
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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[0]
cox_ph
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[0]
time_to_event_with_censoring
evidence object · 3 fields
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1
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quote
Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models.
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id
method-2
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group_comparison
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Group comparison
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[0]
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two_or_more_groups_continuous
evidence object · 3 fields
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0.8
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ANOVA
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id
method-3
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differential_expression
specific
limma_voom
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Differential expression analysis
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[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
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evidence object · 3 fields
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limma
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correlation_analysis
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[0]
spearman_rho
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[0]
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evidence object · 3 fields
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0.8
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Spearman rank correlation
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id
method-5
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diagnostic_evaluation
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Diagnostic test evaluation
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[0]
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[1]
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[3]
solve_confusion_matrix
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evidence object · 3 fields
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[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
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survival_analysis
[3]
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[4]
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[5]
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[6]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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blocked_on
nothing:replicable_now
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cox_ph
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 3 items
[0]
GSE2719
[1]
GSE21050
[2]
GSE30929
resolved_accessions array · 3 items
[0]
GSE2719
[1]
GSE21050
[2]
GSE30929
statements array · 1 item
[0]
All datasets presented in this study are included in the article/Supplementary Material.
basis
The paper names GSE2719, GSE21050, GSE30929 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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[0]
cox_ph
assets array · 2 items
[0]
source:pmid:37100454
[1]
data:geo:GSE21050
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run_analysis
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[0]
data:geo:GSE21050
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:37:44Z
independence
single_reader
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verbatim
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verbatim
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extraction
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minimax
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not_run
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provenance object · 7 fields
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id
pmid:37100454
type
paper
label
pmid:37100454
[1] object · 3 fields
id
source:pmid:37100454
type
manuscript
label
PMID 37100454 full text
[2] object · 3 fields
id
data:geo:GSE21050
type
dataset
label
GEO GSE21050
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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paper
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pmid:37100454
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source:pmid:37100454
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manuscript
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PMID 37100454 full text
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data:geo:GSE21050
type
dataset
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GEO GSE21050
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agent:corpus-assay-engine
[1] object · 4 fields
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extraction
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[0]
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agent:minimax-reader
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activity-resolve-GSE21050
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accession_resolution
used array · 1 item
[0]
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agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
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agent:corpus-assay-engine
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Corpus assay engine
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agent:minimax-reader
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lineage object · 4 fields
parent_id
pmid:37100454
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sha256:1b0e18fc235da7c3f62efabb85d22d38e73d24e6971fc6f74f88800f7813c361
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[3]
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[4]
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[5]
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[6]
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[0] object · 11 fields
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99e1195c7d6f
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[0]
differentially expressed ZNFs. In addition, CCK8 and plate clone formation assays were used t
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paper_text_order:678
id
assay:1
[1] object · 11 fields
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data_generation
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rna_seq
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99e1195c7d6f
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re constructed using the “pheatmap” package. RNA-seq data and clinical information of patients di
[1]
ormatics and statistical analyses, including RNA-seq data normalization and transformation, DEG a
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ZNFs on human chromosomes. Cell culture and transfection A673 and SW982 cell lines were purchased fro
[1]
MAX (Invitrogen, Carlsbad, CA, USA). Then we transfected ZNF141-overexpression-promoting plasmid (GV-
[2]
bovine serum (Biological Industries). ZNF141 siRNA and negative control siRNA oligonucleotides
[3]
dustries). ZNF141 siRNA and negative control siRNA oligonucleotides were designed and synthesiz
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(Shanghai, China). A673 and SW982 cells were cultured in DMEM (Biological Industries, Shanghai, China
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supported
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f2132e96ae6c7a4e
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Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37100454", "kind": "science-record", "revision": 3, "content_hash": "sha256:0b4b4932f526912eea841d5f42e068bab39f5ca8e5840b640b15e22775cb9171", "created_at": "2026-11-01T19:01:46Z", "updated_at": "2026-11-01T22:09:20Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development and validation of novel prognostic models for zinc finger proteins-related genes in soft tissue sarcoma.", "doi": "10.18632/aging.204682", "pmid": "37100454", "authors": ["Junqing Li", "Quan Zhou", "Changsheng Zhang", "Huimin Zhu", "Jie Yao", "Meng Zhang"], "journal": "Aging", "year": 2023, "abstract": "As the most common transcriptional regulators, zinc finer proteins (ZNFs) play vital roles in occurrence and progression of malignant tumors. Whereas, information regarding the roles of ZNFs in soft tissue sarcomas (STS) remains scarce. In this study, a comprehensive bioinformatics analysis investigating roles of ZNFs in STS was performed. Initially, we extracted raw datasets of differentially expressed ZNFs from GSE2719. Using a sequence of bioinformatics methods, we then investigated the prognostic significance, function, and molecular subtype of these differentially expressed ZNFs. In addition, CCK8 and plate clone formation assays were used to explore the effect of ZNF141 on STS cells. A total of 110 differentially expressed ZNFs were identified. Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model. Compared with patients with low-risk in the TCGA training and testing cohorts, as well as the GEO validation cohorts, patients with high-risk had poorer OS and PFS. Using nomograms constructed with the identified ZNFs predicting OS and PFS, we established a clinically useful model. Four distinct molecular subtypes with different prognostic and immune infiltration characteristics were identified. In vitro experiments showed that ZNF141 promoted the proliferation and viability of STS cells. In conclusion, ZNF-related models are useful as prognostic biomarkers, suggesting their potentials as therapeutic targets in STS. These findings will enable us to develop novel strategies treating STS, which will potentially improve outcomes of patients with STS.", "claims": [{"id": "claim-method", "statement": "Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37100454", "locator": "sections[4] \"Construction and validation of prognostic models\" paragraph 3", "quote": "Then factors confirmed by the univariate Cox regression analysis to be significantly associated with prognosis were subsequently incorporated into the LASSO-penalized Cox regression analysis to establish prognostic models."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All datasets presented in this study are included in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37100454", "locator": "sections[12] \"Data availability statement\" paragraph 2", "quote": "All datasets presented in this study are included in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37100454", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Nine ZNFs (HLTF, ZNF292, ZNF141, LDB3, PHF14, ZNF322, PDLIM1, NR3C2, and LIMS2) were selected to establish an overall survival (OS) prediction model, and seven ZNFs (ZIC1, ZNF141, ZHX2, ZNF281, ZNHIT2, NR3C2, and LIMS2) were used to develop a progression-free survival (PFS) prediction model.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37100454"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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