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pmid:34440557

Novel Therapies for Tongue Squamous Cell Carcinoma Patients with High-Grade Tumors.

Yinghua Li · Hao Lin · Lu Chen · Zihao Chen · Weizhong Li

Life (Basel, Switzerland) · 2021 doi:10.3390/life11080813

Paper

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complete

Data

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partial

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title
Novel Therapies for Tongue Squamous Cell Carcinoma Patients with High-Grade Tumors.
doi
10.3390/life11080813
pmid
34440557
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[0]
Yinghua Li
[1]
Hao Lin
[2]
Lu Chen
[3]
Zihao Chen
[4]
Weizhong Li
journal
Life (Basel, Switzerland)
year
2021
abstract
BACKGROUND: Tongue squamous cell carcinoma (TSCC) patients with high-grade tumors usually suffer from high occurrence and poor prognosis. The current study aimed at finding the biomarkers related to tumor grades and proposing potential therapies by these biomarkers. METHODS: The mRNA expression matrix of TSCC samples from The Cancer Genome Atlas (TCGA) database was analyzed to identify hub proteins related to tumor grades. The mRNA expression patterns of these hub proteins between TSCC and adjacent control samples were validated in three independent TSCC data sets (i.e., GSE9844, GSE30784, and GSE13601). The correlation between cell cycle index and immunotherapy efficacy was tested on the IMvigor210 data set. Based on the structure of hub proteins, virtual screening was applied to compounds to find the potential inhibitors. RESULTS: A total of six cell cycle biomarkers (i.e., BUB1, CCNB2, CDC6, CDC20, CDK1, and MCM2) were selected as hub proteins by protein-protein interaction (PPI) analysis. In the validation data sets, the mRNA expression levels of these hub proteins were higher in tumor samples versus normal controls. The cell cycle index was constructed by the mRNA expression levels of these hub proteins, and patients with a high cell cycle index demonstrated favorable drug response to the immunotherapy. Three small molecules (i.e., ZINC100052685, ZINC8214703, and ZINC85537014) were found to bind with hub proteins and selected as drug candidates. CONCLUSION: The cell cycle index might provide a novel reference for selecting appropriate cancer patient candidates for immunotherapy. The current research might contribute to the development of precision medicine and improve the prognosis of TSCC.
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DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05).
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sections[4] "2.2. Selection of Grade-Associated Genes" paragraph 2
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DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05).
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Publicly available datasets from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were analyzed in this study. This data from TCGA can be found here: https://portal.gdc.cancer.gov/ (accessed on 15 June 2021). This data from GEO can be found here: https://www.ncbi.nlm.nih.gov/geo/ (accessed on 15 June 2021). All the datasets could be downloaded without any limitations.
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Publicly available datasets from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were analyzed in this study. This data from TCGA can be found here: https://portal.gdc.cancer.gov/ (accessed on 15 June 2021). This data from GEO can be found here: https://www.ncbi.nlm.nih.gov/geo/ (accessed on 15 June 2021). All the datasets could be downloaded without any limitations.
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Oral tongue cancer gene expression profiling: Identification of novel potential prognosticators
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<0.01
[3]
11
[6] array · 4 items
[0]
GO_BP:0048285
[1]
Organelle Fission
[2]
<0.01
[3]
48
[7] array · 4 items
[0]
GO_BP:0000280
[1]
Nuclear Division
[2]
<0.01
[3]
47
[8] array · 4 items
[0]
GO_BP:0007059
[1]
Chromosome Segregation
[2]
<0.01
[3]
45
[9] array · 4 items
[0]
GO_BP:0140014
[1]
Mitotic Nuclear Division
[2]
<0.01
[3]
42
[10] array · 4 items
[0]
GO_BP:0043062
[1]
Extracellular Structure Organization
[2]
<0.01
[3]
40
[11] array · 4 items
[0]
GO_CC:0031012
[1]
Extracellular Matrix
[2]
<0.01
[3]
41
[12] array · 4 items
[0]
GO_CC:0005819
[1]
Spindle
[2]
<0.01
[3]
38
[13] array · 4 items
[0]
GO_CC:0062023
[1]
Collagen-containing Extracellular Matrix
[2]
<0.01
[3]
38
[14] array · 4 items
[0]
GO_CC:0098687
[1]
Chromosomal Region
[2]
<0.01
[3]
33
[15] array · 4 items
[0]
GO_CC:0000775
[1]
Chromosome, Centromeric Region
[2]
<0.01
[3]
28
[16] array · 4 items
[0]
GO_MF:0048037
[1]
Cofactor Binding
[2]
<0.01
[3]
28
[17] array · 4 items
[0]
GO_MF:0003779
[1]
Actin Binding
[2]
<0.01
[3]
24
[18] array · 4 items
[0]
GO_MF:0050662
[1]
Coenzyme Binding
[2]
<0.01
[3]
22
[19] array · 4 items
[0]
GO_MF:0005201
[1]
Extracellular Matrix Structural Constituent
[2]
<0.01
[3]
19
[20] array · 4 items
[0]
GO_MF:1901681
[1]
Sulfur Compound Binding
[2]
<0.01
[3]
18
locator
section[13]/table-wrap[1]#life-11-00813-t001
[5] object · 16 fields
id
asset:table:pmid:34440557:2
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table
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jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:4a6682417b8bad36a9c05cfd04e2fe1e955a7acfed023d88cc9d064ae5995882
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verified
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read_table
reader_status
available
identifier
section[14]/table-wrap[1]#life-11-00813-t002
version
null
note
Comparing mRNA expression levels of hub proteins between tumor and normal samples groups by Wilcoxon test.
structure object · 5 fields
pmcid
PMC8398384
section_index
14
section_title
3.3. Protein–Protein Interaction (PPI) and Hub Proteins
row_count
5
column_count
7
table object · 8 fields
label
Table 2
caption
Comparing mRNA expression levels of hub proteins between tumor and normal samples groups by Wilcoxon test.
rows array · 5 items
[0] array · 7 items
[0]
Datasets\Genes
[1]
BUB1
[2]
CCNB2
[3]
CDC6
[4]
CDC20
[5]
CDK1
[6]
MCM2
[1] array · 7 items
[0]
TSCC (TCGA)
[1]
p < 0.01
[2]
p < 0.01
[3]
p < 0.01
[4]
p < 0.01
[5]
p < 0.01
[6]
p < 0.01
[2] array · 7 items
[0]
GSE30784
[1]
p < 0.01
[2]
p < 0.01
[3]
p < 0.01
[4]
p < 0.01
[5]
p < 0.01
[6]
p < 0.01
[3] array · 7 items
[0]
GSE9844
[1]
0.23
[2]
0.019
[3]
p < 0.01
[4]
p < 0.01
[5]
0.033
[6]
p < 0.01
[4] array · 7 items
[0]
GSE13601
[1]
p < 0.01
[2]
p < 0.01
[3]
0.14
[4]
p < 0.01
[5]
p < 0.01
[6]
p < 0.01
locator
section[14]/table-wrap[1]#life-11-00813-t002
[6] object · 16 fields
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asset:table:pmid:34440557:3
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table
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jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:3d0657d2026696d1e87be1aa2e0fa0e819e414b098a0b0aee00609c5bc007d75
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read_table
reader_status
available
identifier
section[17]/table-wrap[1]#life-11-00813-t003
version
null
note
The compounds with the highest Libdock score.
structure object · 5 fields
pmcid
PMC8398384
section_index
17
section_title
3.6. Virtual Screening of Compounds
row_count
10
column_count
3
table object · 8 fields
label
Table 3
caption
The compounds with the highest Libdock score.
rows array · 10 items
[0] array · 3 items
[0]
Protein
[1]
ZincID
[2]
Libdock Score
[1] array · 3 items
[0]
CDC20
[1]
ZINC3799072
[2]
116.1
[2] array · 3 items
[0]
CDC20
[1]
ZINC100052685
[2]
105.9
[3] array · 3 items
[0]
CDC20
[1]
ZINC3785268
[2]
105.6
[4] array · 3 items
[0]
CDK1
[1]
ZINC8214703
[2]
126.7
[5] array · 3 items
[0]
CDK1
[1]
ZINC21297660
[2]
113.4
[6] array · 3 items
[0]
CDK1
[1]
ZINC601250
[2]
111.8
[7] array · 3 items
[0]
MCM2
[1]
ZINC28232755
[2]
171.2
[8] array · 3 items
[0]
MCM2
[1]
ZINC85537014
[2]
166.8
[9] array · 3 items
[0]
MCM2
[1]
ZINC28639340
[2]
161.7
locator
section[17]/table-wrap[1]#life-11-00813-t003
[7] object · 16 fields
id
asset:table:pmid:34440557:4
role
table
format
jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:15a0ed42ea80af1df8113d1a8f97f09ea95160a4fa661e786cfce60aec193300
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verified
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read_table
reader_status
available
identifier
section[18]/table-wrap[1]#life-11-00813-t004
version
null
note
Adsorption, distribution, metabolism, and excretion properties of compounds.
structure object · 5 fields
pmcid
PMC8398384
section_index
18
section_title
3.7. Pharmacologic Properties of Compounds
row_count
10
column_count
7
table object · 8 fields
label
Table 4
caption
Adsorption, distribution, metabolism, and excretion properties of compounds.
rows array · 10 items
[0] array · 7 items
[0]
Compounds
[1]
Solubility Level
[2]
BBB Level
[3]
CYP2D6
[4]
Hepatotoxicity
[5]
Absorption Level
[6]
PPB Level
[1] array · 7 items
[0]
ZINC3799072
[1]
3
[2]
2
[3]
1
[4]
0
[5]
0
[6]
1
[2] array · 7 items
[0]
ZINC100052685
[1]
2
[2]
4
[3]
0
[4]
0
[5]
1
[6]
1
[3] array · 7 items
[0]
ZINC3785268
[1]
3
[2]
2
[3]
1
[4]
0
[5]
0
[6]
1
[4] array · 7 items
[0]
ZINC8214703
[1]
3
[2]
4
[3]
0
[4]
0
[5]
0
[6]
1
[5] array · 7 items
[0]
ZINC21297660
[1]
3
[2]
3
[3]
0
[4]
0
[5]
0
[6]
1
[6] array · 7 items
[0]
ZINC601250
[1]
1
[2]
0
[3]
1
[4]
1
[5]
1
[6]
1
[7] array · 7 items
[0]
ZINC28232755
[1]
1
[2]
4
[3]
0
[4]
0
[5]
3
[6]
0
[8] array · 7 items
[0]
ZINC85537014
[1]
3
[2]
4
[3]
1
[4]
1
[5]
2
[6]
0
[9] array · 7 items
[0]
ZINC28639340
[1]
3
[2]
4
[3]
0
[4]
1
[5]
2
[6]
1
locator
section[18]/table-wrap[1]#life-11-00813-t004
[8] object · 16 fields
id
asset:table:pmid:34440557:5
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table
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jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:e66ceb7a65e772875313a5bb2375fce3c49a18425181b7bec33bb10b028593f6
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654
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verified
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read_table
reader_status
available
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section[18]/table-wrap[2]#life-11-00813-t005
version
null
note
Toxicities of compounds.
structure object · 5 fields
pmcid
PMC8398384
section_index
18
section_title
3.7. Pharmacologic Properties of Compounds
row_count
10
column_count
7
table object · 8 fields
label
Table 5
caption
Toxicities of compounds.
rows array · 10 items
[0] array · 7 items
[0]
Compounds
[1]
Mouse NTP (Female)
[2]
Mouse NTP(Male)
[3]
Rat NTP(Female)
[4]
Rat NTP(Male)
[5]
Ames
[6]
DTP
[1] array · 7 items
[0]
ZINC3799072
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
1
[2] array · 7 items
[0]
ZINC100052685
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
0
[3] array · 7 items
[0]
ZINC3785268
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
1
[4] array · 7 items
[0]
ZINC8214703
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
0
[5] array · 7 items
[0]
ZINC21297660
[1]
0
[2]
1
[3]
0
[4]
1
[5]
0
[6]
1
[6] array · 7 items
[0]
ZINC601250
[1]
0
[2]
1
[3]
0
[4]
0
[5]
0
[6]
1
[7] array · 7 items
[0]
ZINC28232755
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
1
[8] array · 7 items
[0]
ZINC85537014
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
0
[9] array · 7 items
[0]
ZINC28639340
[1]
0
[2]
0
[3]
0
[4]
0
[5]
0
[6]
1
locator
section[18]/table-wrap[2]#life-11-00813-t005
[9] object · 16 fields
id
asset:table:pmid:34440557:6
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table
format
jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:2ee81c1531bff65aa7f6e0b762c3044841e01efeb8bc29f2de563f1fbc3536b1
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1159
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verified
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read_table
reader_status
available
identifier
section[22]/table-wrap[1]#array1
version
null
note
null
structure object · 5 fields
pmcid
PMC8398384
section_index
22
section_title
Abbreviations
row_count
26
column_count
2
table object · 8 fields
label
null
caption
null
rows array · 26 items
[0] array · 2 items
[0]
TSCC
[1]
Tongue squamous cell carcinoma
[1] array · 2 items
[0]
OSCC
[1]
oral squamous cell carcinoma
[2] array · 2 items
[0]
TCGA
[1]
The Cancer Genome Atlas
[3] array · 2 items
[0]
CDKs
[1]
cyclin-dependent kinases
[4] array · 2 items
[0]
DEGs
[1]
differentially expressed genes
[5] array · 2 items
[0]
PPI
[1]
protein–protein interaction
[6] array · 2 items
[0]
ORR
[1]
objective response rate
[7] array · 2 items
[0]
KEGG
[1]
Kyoto Encyclopedia of genes and Genomes
[8] array · 2 items
[0]
GO
[1]
Gene Ontology
[9] array · 2 items
[0]
BP
[1]
biological process
[10] array · 2 items
[0]
CC
[1]
cellular component
[11] array · 2 items
[0]
MF
[1]
molecular function
[12] array · 2 items
[0]
OS
[1]
overall survival
[13] array · 2 items
[0]
ssGSEA
[1]
single sample gene set enrichment analysis
[14] array · 2 items
[0]
PDB
[1]
Protein Data Bank
[15] array · 2 items
[0]
ADMET
[1]
adsorption, distribution, metabolism, excretion, and toxicity
[16] array · 2 items
[0]
DTP
[1]
developmental toxicity potential
[17] array · 2 items
[0]
BUB1
[1]
budding uninhibited by benzimidazoles 1
[18] array · 2 items
[0]
CCNB2
[1]
cyclin B2
[19] array · 2 items
[0]
CDC6
[1]
cell division cycle 6
[20] array · 2 items
[0]
CDC20
[1]
cell division cycle 20
[21] array · 2 items
[0]
CDK1
[1]
cyclin dependent kinase 1
[22] array · 2 items
[0]
MCM2
[1]
minichromosome maintenance complex component 2
[23] array · 2 items
[0]
TMB
[1]
tumor mutational burden
[24] array · 2 items
[0]
EMT
[1]
epithelial-to-mesenchymal transition
[25] array · 2 items
[0]
HIV
[1]
human immunodeficiency virus
locator
section[22]/table-wrap[1]#array1
gaps array · 6 items
[0]
asset:data:geo:GSE13601 not downloaded
[1]
asset:data:geo:GSE13601 licence not read
[2]
asset:data:geo:GSE30784 not downloaded
[3]
asset:data:geo:GSE30784 licence not read
[4]
asset:data:geo:GSE9844 not downloaded
[5]
asset:data:geo:GSE9844 licence not read
analysis object · 4 fields
state
partial
methods array · 5 items
[0] object · 10 fields
id
method-1
family
correlation_analysis
specific
pearson
label
Correlation analysis
dsl_operations array · 1 item
[0]
pearson_r
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
score
1
band
verbatim
quote
DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05).
[1] object · 10 fields
id
method-2
family
group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[2] object · 10 fields
id
method-3
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
band
high
quote
Kaplan-Meier
[3] object · 10 fields
id
method-4
family
differential_expression
specific
edger
label
Differential expression analysis
dsl_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
count_matrix_with_condition
evidence object · 3 fields
score
0.8
band
high
quote
edgeR
[4] object · 10 fields
id
method-5
family
network_analysis
specific
ppi_network
label
Network / pathway analysis
dsl_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.7
band
medium
quote
protein-protein interaction
targets array · 0 items
gaps array · 1 item
[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
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 1 item
[0]
pearson_r
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: pearson.
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]
GSE9844
[1]
GSE30784
[2]
GSE13601
resolved_accessions array · 3 items
[0]
GSE9844
[1]
GSE30784
[2]
GSE13601
statements array · 1 item
[0]
Publicly available datasets from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were analyzed in this study. This data from TCGA can be found here: https://portal.gdc.cancer.gov/ (accessed on 15 June 2021). This data from GEO can be found here: https://www.ncbi.nlm.nih.gov/geo/ (accessed on 15 June 2021). All the datasets could be downloaded without any limitations.
basis
The paper names GSE9844, GSE30784, GSE13601 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
[0]
pearson_r
assets array · 8 items
[0]
source:pmid:34440557
[1]
data:geo:GSE13601
[2]
asset:table:pmid:34440557:1
[3]
asset:table:pmid:34440557:2
[4]
asset:table:pmid:34440557:3
[5]
asset:table:pmid:34440557:4
[6]
asset:table:pmid:34440557:5
[7]
asset:table:pmid:34440557:6
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE13601
gaps array · 0 items
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
2026-10-31T18:34:08Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
3
usage object · 3 fields
prompt_tokens
38307
completion_tokens
2361
cached_tokens
776
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:34440557
type
paper
label
pmid:34440557
[1] object · 3 fields
id
source:pmid:34440557
type
manuscript
label
PMID 34440557 full text
[2] object · 3 fields
id
data:geo:GSE13601
type
dataset
label
GEO GSE13601
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
id
pmid:34440557
type
paper
label
pmid:34440557
[1] object · 3 fields
id
source:pmid:34440557
type
manuscript
label
PMID 34440557 full text
[2] object · 3 fields
id
data:geo:GSE13601
type
dataset
label
GEO GSE13601
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-34440557
type
extraction
used array · 1 item
[0]
source:pmid:34440557
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE13601
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE13601
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:34440557
parent_hash
sha256:30613560427a4465f89f94c71e97448196601d08547b938a5d0914aa2e09830b
fork_of
null
gaps array · 11 items
[0]
asset:data:geo:GSE13601 licence not read
[1]
asset:data:geo:GSE13601 not downloaded
[2]
asset:data:geo:GSE30784 licence not read
[3]
asset:data:geo:GSE30784 not downloaded
[4]
asset:data:geo:GSE9844 licence not read
[5]
asset:data:geo:GSE9844 not downloaded
[6]
execution.not_run
[7]
method.reader_differs_from_extractor
[8]
review.human_critique
[9]
review.independent_reader
[10]
review.machine_critique
assays array · 2 items
[0] object · 11 fields
role
data_generation
definition_id
rna_seq
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.93
evidence array · 1 item
[0]
the first group was a TCGA–TSCC dataset. The RNA sequencing data profiles and clinical information of 13
order_basis
paper_text_order:2006
id
assay:1
[1] object · 11 fields
role
analysis
definition_id
correlation_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
pearson_r
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05).
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34440557", "kind": "science-record", "revision": 7, "content_hash": "sha256:98cb9e4ca163572e06bb3a9999a2c30860bbd7d7d0989bd7bd68f3480004e30c", "created_at": "2026-11-01T15:41:49Z", "updated_at": "2026-11-01T22:04:34Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Novel Therapies for Tongue Squamous Cell Carcinoma Patients with High-Grade Tumors.", "doi": "10.3390/life11080813", "pmid": "34440557", "authors": ["Yinghua Li", "Hao Lin", "Lu Chen", "Zihao Chen", "Weizhong Li"], "journal": "Life (Basel, Switzerland)", "year": 2021, "abstract": "BACKGROUND: Tongue squamous cell carcinoma (TSCC) patients with high-grade tumors usually suffer from high occurrence and poor prognosis. The current study aimed at finding the biomarkers related to tumor grades and proposing potential therapies by these biomarkers.\nMETHODS: The mRNA expression matrix of TSCC samples from The Cancer Genome Atlas (TCGA) database was analyzed to identify hub proteins related to tumor grades. The mRNA expression patterns of these hub proteins between TSCC and adjacent control samples were validated in three independent TSCC data sets (i.e., GSE9844, GSE30784, and GSE13601). The correlation between cell cycle index and immunotherapy efficacy was tested on the IMvigor210 data set. Based on the structure of hub proteins, virtual screening was applied to compounds to find the potential inhibitors.\nRESULTS: A total of six cell cycle biomarkers (i.e., BUB1, CCNB2, CDC6, CDC20, CDK1, and MCM2) were selected as hub proteins by protein-protein interaction (PPI) analysis. In the validation data sets, the mRNA expression levels of these hub proteins were higher in tumor samples versus normal controls. The cell cycle index was constructed by the mRNA expression levels of these hub proteins, and patients with a high cell cycle index demonstrated favorable drug response to the immunotherapy. Three small molecules (i.e., ZINC100052685, ZINC8214703, and ZINC85537014) were found to bind with hub proteins and selected as drug candidates.\nCONCLUSION: The cell cycle index might provide a novel reference for selecting appropriate cancer patient candidates for immunotherapy. The current research might contribute to the development of precision medicine and improve the prognosis of TSCC.", "claims": [{"id": "claim-method", "statement": "DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34440557", "locator": "sections[4] \"2.2. Selection of Grade-Associated Genes\" paragraph 2", "quote": "DEGs were chosen by differential expression analysis among tumor grades using the Kruskal–Wallis rank-sum test (p-value < 0.05)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available datasets from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were analyzed in this study. This data from TCGA can be found here: https://portal.gdc.cancer.gov/ (accessed on 15 June 2021). This data from GEO can be found here: https://www.ncbi.nlm.nih.gov/geo/ (accessed on 15 June 2021). 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13601"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13601"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34440557", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3390/life11080813", "sha256": "sha256:40de76879ca55e7b2afe02d8194d24a476fb483172b9b8d8875f957384d658df", "bytes": 47118, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3390/life11080813", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC8398384", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE13601", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE13601", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE13601", "version": null, "note": "Publicly available datasets from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were analyzed in this study. 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