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pmid:33552736

Identification of an immune prognostic 11-gene signature for lung adenocarcinoma.

Tao Yang · Lizheng Hao · Renyun Cui · Huanyu Liu · Jian Chen · Jiongjun An · Shuo Qi · Zhong Li

PeerJ · 2021 doi:10.7717/peerj.10749

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title
Identification of an immune prognostic 11-gene signature for lung adenocarcinoma.
doi
10.7717/peerj.10749
pmid
33552736
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[0]
Tao Yang
[1]
Lizheng Hao
[2]
Renyun Cui
[3]
Huanyu Liu
[4]
Jian Chen
[5]
Jiongjun An
[6]
Shuo Qi
[7]
Zhong Li
journal
PeerJ
year
2021
abstract
BACKGROUND: The immunological tumour microenvironment (TME) has occupied a very important position in the beginning and progression of non-small cell lung cancer (NSCLC). Prognosis of lung adenocarcinoma (LUAD) remains poor for the local progression and widely metastases at the time of clinical diagnosis. Our objective is to identify a potential signature model to improve prognosis of LUAD. METHODS: With the aim to identify a novel immune prognostic signature associated with overall survival (OS), we analysed LUADs extracted from The Cancer Genome Atlas (TCGA). Immune scores and stromal scores of TCGA-LUAD were downloaded from Estimation of STromal and Immune cells in MAlignant Tumour tissues Expression using data (ESTIMATE). LASSO COX regression was applied to build the prediction model. Then, the prognostic gene signature was validated in the GSE68465 dataset. RESULTS: The data from TCGA datasets showed patients in stage I and stage II had higher stromal scores than patients in stage IV (P < 0.05), and for immune score patients in stage I were higher than patients in stage III and stage IV (P < 0.05). The improved overall survivals were observed in high stromal score and immune score groups. Patients in the high-risk group exhibited the inferior OS (P = 2.501e - 05). By validating the 397 LUAD patients from GSE68465, we observed a better OS in the low-risk group compared to the high-risk group, which is consistent with the results from the TCGA cohort. Nomogram results showed that practical and predicted survival coincided very well, especially for 3-year survival. CONCLUSION: We obtained an 11 immune score related gene signature model as an independent element to effectively classify LUADs into different risk groups, which might provide a support for precision treatments. Moreover, immune score may play a potential valuable sole for estimating OS in LUADs.
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The following information was supplied regarding data availability: The raw measurements are available in the Supplemental Files. TCGA-LUAD mRNA FPKM data is available at Figshare: Hao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.
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sections[31] "Data Availability Statement" paragraphs 1-5
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The following information was supplied regarding data availability: The raw measurements are available in the Supplemental Files. TCGA-LUAD mRNA FPKM data is available at Figshare: Hao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.
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The following information was supplied regarding data availability: The raw measurements are available in the Supplemental Files. TCGA-LUAD mRNA FPKM data is available at Figshare: Hao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.
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The following information was supplied regarding data availability: The raw measurements are available in the Supplemental Files. TCGA-LUAD mRNA FPKM data is available at Figshare: Hao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.
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section[12]/table-wrap[1]#table-1
version
null
note
Top 10 terms of BP, MF, CC.
structure object · 5 fields
pmcid
PMC7825366
section_index
12
section_title
Identification and selection of the immunological TME related DEGs and GO analysis
row_count
31
column_count
4
table object · 8 fields
label
Table 1
caption
Top 10 terms of BP, MF, CC.
rows array · 31 items
[0] array · 4 items
[0]
Category
[1]
GO-ID
[2]
GO-Term
[3]
Adj P value
[1] array · 4 items
[0]
MF
[1]
GO0003823
[2]
Antigen binding
[3]
2.82E−29
[2] array · 4 items
[0]
MF
[1]
GO0005125
[2]
Cytokine activity
[3]
1.98E−12
[3] array · 4 items
[0]
MF
[1]
GO0004896
[2]
Cytokine receptor activity
[3]
5.95E−12
[4] array · 4 items
[0]
MF
[1]
GO0042287
[2]
MHC protein binding
[3]
3.85E−10
[5] array · 4 items
[0]
MF
[1]
GO0008009
[2]
Chemokine activity
[3]
4.74E−10
[6] array · 4 items
[0]
MF
[1]
GO0030246
[2]
Carbohydrate binding
[3]
1.33E−09
[7] array · 4 items
[0]
MF
[1]
GO0042379
[2]
Chemokine receptor binding
[3]
3.36E−09
[8] array · 4 items
[0]
MF
[1]
GO0005126
[2]
Cytokine receptor binding
[3]
4.14E−09
[9] array · 4 items
[0]
MF
[1]
GO0048020
[2]
CCR chemokine receptor binding
[3]
8.63E−09
[10] array · 4 items
[0]
MF
[1]
GO0034987
[2]
Immunoglobulin receptor binding
[3]
2.28E−08
[11] array · 4 items
[0]
BP
[1]
GO0002429
[2]
Immune response-activating cell surface receptor signaling pathway
[3]
1.94E−56
[12] array · 4 items
[0]
BP
[1]
GO0051249
[2]
Regulation of lymphocyte activation
[3]
1.94E−56
[13] array · 4 items
[0]
BP
[1]
GO0042110
[2]
T cell activation
[3]
1.58E−52
[14] array · 4 items
[0]
BP
[1]
GO0002460
[2]
Adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains
[3]
2.32E−44
[15] array · 4 items
[0]
BP
[1]
GO0050867
[2]
Positive regulation of cell activation
[3]
2.7E−44
[16] array · 4 items
[0]
BP
[1]
GO0002696
[2]
Positive regulation of leukocyte activation
[3]
1.07E−43
[17] array · 4 items
[0]
BP
[1]
GO0050863
[2]
Regulation of T cell activation
[3]
3.29E−42
[18] array · 4 items
[0]
BP
[1]
GO0007159
[2]
Leukocyte cell–cell adhesion
[3]
6.12E−41
[19] array · 4 items
[0]
BP
[1]
GO0070661
[2]
Leukocyte proliferation
[3]
6.89E−41
[20] array · 4 items
[0]
BP
[1]
GO0046651
[2]
Lymphocyte proliferation
[3]
1.23E−40
[21] array · 4 items
[0]
CC
[1]
GO0042101
[2]
T cell receptor complex
[3]
5.35E−54
[22] array · 4 items
[0]
CC
[1]
GO0098802
[2]
Plasma membrane receptor complex
[3]
3.06E−46
[23] array · 4 items
[0]
CC
[1]
GO0009897
[2]
External side of plasma membrane
[3]
1.4E−45
[24] array · 4 items
[0]
CC
[1]
GO0019814
[2]
Immunoglobulin complex
[3]
8.93E−35
[25] array · 4 items
[0]
CC
[1]
GO0042613
[2]
MHC class II protein complex
[3]
5.75E−12
[26] array · 4 items
[0]
CC
[1]
GO0070820
[2]
Tertiary granule
[3]
2.3E−09
[27] array · 4 items
[0]
CC
[1]
GO0042611
[2]
MHC protein complex
[3]
3.26E−09
[28] array · 4 items
[0]
CC
[1]
GO0001772
[2]
Immunological synapse
[3]
1.82E−08
[29] array · 4 items
[0]
CC
[1]
GO0042571
[2]
Immunoglobulin complex, circulating
[3]
1.58E−07
[30] array · 4 items
[0]
CC
[1]
GO0042581
[2]
Specific granule
[3]
7.85E−07
locator
section[12]/table-wrap[1]#table-1
[3] object · 16 fields
id
asset:table:pmid:33552736:2
role
table
format
jats-table
media_type
application/vnd.jats.table+json
uri
null
sha256
sha256:c8b2d1bd0c01fdc1215291a253152792a6450ca17076cae5f6efb9b50f4f1360
bytes
1839
access
open
state
verified
reader
read_table
reader_status
available
identifier
section[18]/table-wrap[1]#table-2
version
null
note
The biological functions of the coding genes.
structure object · 5 fields
pmcid
PMC7825366
section_index
18
section_title
Discussion
row_count
12
column_count
2
table object · 8 fields
label
Table 2
caption
The biological functions of the coding genes.
rows array · 12 items
[0] array · 2 items
[0]
Gene
[1]
Immune-related functions
[1] array · 2 items
[0]
CD70
[1]
CD70 belongs to TNF ligand family and can enhance the generation of cytolytic T cells and induce proliferation of co-stimulated T cells (Keller et al., 2007; Kuka et al., 2013). The regulatory mechanisms for the CD70-CD27 pathway is critical for prognosis of cancer patients.
[2] array · 2 items
[0]
CXorf21
[1]
CXorf21 is a mediator of the X-chromosome gene of systemic lupus erythematosus in female (Bentham et al., 2015; Harris et al., 2019b) and is expressed only in immune cell (Harris et al., 2019a).
[3] array · 2 items
[0]
CD74
[1]
CD74 expression serves as a prognostic factor in many cancers (Ekmekcioglu et al., 2016; Otterstrom et al., 2014; Ruvolo et al., 2019; Zeiner et al., 2015; Zeiner et al., 2018; Zhang et al., 2014).
[4] array · 2 items
[0]
RUBCNL
[1]
RUBCNL is a vertebrate-specific autophagy regulator (Cheng et al., 2017), and involves autophagy in NSCLC (Levy, Towers & Thorburn, 2017).
[5] array · 2 items
[0]
BIRC3
[1]
BIRC3 involves in the prognostication system in Chronic Lymphocytic Leukemia (Alhourani et al., 2016) and hepatocellular carcinoma patients undergoing curative resection (Fu et al., 2019).
[6] array · 2 items
[0]
TESC
[1]
TESC can reinforce the radio-resistant properties of NSCLC (Lee et al., 2018).
[7] array · 2 items
[0]
INSL4
[1]
Abnormal INSL4 signaling may act as a promising therapeutic target for LKB1-deficient NSCLC (Yang et al., 2018).
[8] array · 2 items
[0]
HLA-DOB
[1]
HLA-DOB are expressed in antigen presenting cells which is tightly linked with the immunity.
[9] array · 2 items
[0]
CIITA
[1]
The vaccination with CIITA-tumour cells is constructed to facilitate anti-tumour cells to enhance the immune system (Accolla et al., 2019).
[10] array · 2 items
[0]
STAP1
[1]
No relevant report yet.
[11] array · 2 items
[0]
OBP2A
[1]
No relevant report yet.
locator
section[18]/table-wrap[1]#table-2
gaps array · 2 items
[0]
asset:data:geo:GSE68465 not downloaded
[1]
asset:data:geo:GSE68465 licence not read
analysis object · 4 fields
state
complete
methods array · 3 items
[0] object · 10 fields
id
method-1
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
dsl_operations array · 1 item
[0]
cox_ph
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
1
band
reordered
quote
“LASSO COX regression was applied to build the prediction model.”
[1] object · 10 fields
id
method-2
family
network_analysis
specific
pathway_enrichment
label
Network / pathway analysis
dsl_operations array · 1 item
[0]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
quote
GO enrichment
[2] object · 10 fields
id
method-3
family
diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
dsl_operations array · 6 items
[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
score
0.8
band
high
quote
ROC curve
targets array · 0 items
gaps array · 0 items
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]
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 · 1 item
[0]
GSE68465
resolved_accessions array · 1 item
[0]
GSE68465
statements array · 1 item
[0]
The following information was supplied regarding data availability: The raw measurements are available in the Supplemental Files. TCGA-LUAD mRNA FPKM data is available at Figshare: Hao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.
basis
The paper names GSE68465 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]
cox_ph
assets array · 4 items
[0]
source:pmid:33552736
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data:geo:GSE68465
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asset:table:pmid:33552736:1
[3]
asset:table:pmid:33552736:2
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:GSE68465
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
2026-10-31T18:27:06Z
independence
single_reader
evidence_check object · 2 fields
method
reordered
availability
verbatim
calls
3
usage object · 3 fields
prompt_tokens
42199
completion_tokens
2436
cached_tokens
784
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
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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:33552736
type
paper
label
pmid:33552736
[1] object · 3 fields
id
source:pmid:33552736
type
manuscript
label
PMID 33552736 full text
[2] object · 3 fields
id
data:geo:GSE68465
type
dataset
label
GEO GSE68465
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
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paper
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pmid:33552736
[1] object · 3 fields
id
source:pmid:33552736
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PMID 33552736 full text
[2] object · 3 fields
id
data:geo:GSE68465
type
dataset
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GEO GSE68465
agent
agent:corpus-assay-engine
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id
activity-read-33552736
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extraction
used array · 1 item
[0]
source:pmid:33552736
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE68465
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE68465
agent
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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MiniMax literature reader
source_run_id
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
parent_id
pmid:33552736
parent_hash
sha256:ddbb371d7d88e4954c5e870fe934079f223f6f1c791a35e7e6e147360fdecd2b
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null
gaps array · 6 items
[0]
asset:data:geo:GSE68465 licence not read
[1]
asset:data:geo:GSE68465 not downloaded
[2]
execution.not_run
[3]
review.human_critique
[4]
review.independent_reader
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assays array · 1 item
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role
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supported
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dsl_catalogue
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“LASSO COX regression was applied to build the prediction model.”
order_basis
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33552736", "kind": "science-record", "revision": 7, "content_hash": "sha256:a273dd0db74e1bf8d2da93cee537aec8ba5f18f008dcdd8d825b4d98bd77ae70", "created_at": "2026-11-01T15:41:24Z", "updated_at": "2026-11-01T22:03:04Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of an immune prognostic 11-gene signature for lung adenocarcinoma.", "doi": "10.7717/peerj.10749", "pmid": "33552736", "authors": ["Tao Yang", "Lizheng Hao", "Renyun Cui", "Huanyu Liu", "Jian Chen", "Jiongjun An", "Shuo Qi", "Zhong Li"], "journal": "PeerJ", "year": 2021, "abstract": "BACKGROUND: The immunological tumour microenvironment (TME) has occupied a very important position in the beginning and progression of non-small cell lung cancer (NSCLC). Prognosis of lung adenocarcinoma (LUAD) remains poor for the local progression and widely metastases at the time of clinical diagnosis. Our objective is to identify a potential signature model to improve prognosis of LUAD.\nMETHODS: With the aim to identify a novel immune prognostic signature associated with overall survival (OS), we analysed LUADs extracted from The Cancer Genome Atlas (TCGA). Immune scores and stromal scores of TCGA-LUAD were downloaded from Estimation of STromal and Immune cells in MAlignant Tumour tissues Expression using data (ESTIMATE). LASSO COX regression was applied to build the prediction model. Then, the prognostic gene signature was validated in the GSE68465 dataset.\nRESULTS: The data from TCGA datasets showed patients in stage I and stage II had higher stromal scores than patients in stage IV (P < 0.05), and for immune score patients in stage I were higher than patients in stage III and stage IV (P < 0.05). The improved overall survivals were observed in high stromal score and immune score groups. Patients in the high-risk group exhibited the inferior OS (P = 2.501e - 05). By validating the 397 LUAD patients from GSE68465, we observed a better OS in the low-risk group compared to the high-risk group, which is consistent with the results from the TCGA cohort. Nomogram results showed that practical and predicted survival coincided very well, especially for 3-year survival.\nCONCLUSION: We obtained an 11 immune score related gene signature model as an independent element to effectively classify LUADs into different risk groups, which might provide a support for precision treatments. Moreover, immune score may play a potential valuable sole for estimating OS in LUADs.", "claims": [{"id": "claim-data-access", "statement": "The following information was supplied regarding data availability:\nThe raw measurements are available in the Supplemental Files.\nTCGA-LUAD mRNA FPKM data is available at Figshare:\nHao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33552736", "locator": "sections[31] \"Data Availability Statement\" paragraphs 1-5", "quote": "The following information was supplied regarding data availability:\nThe raw measurements are available in the Supplemental Files.\nTCGA-LUAD mRNA FPKM data is available at Figshare:\nHao, Lizheng (2021): dat2.zip. figshare. Dataset. https://doi.org/10.6084/m9.figshare.13515998.v1."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "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:33552736"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE68465"], "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:GSE68465"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:33552736", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.7717/peerj.10749", "sha256": "sha256:947602c3d90a6344f50235df8bbfc00e7373a60e69ee97e1b2662656e3506739", "bytes": 50598, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.7717/peerj.10749", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC7825366", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE68465", "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=GSE68465", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE68465", "version": null, "note": "The following information was supplied regarding data availability:\nThe raw measurements are available in the Supplemental Files.\nTCGA-LUAD mRNA FPKM data is available at Figshare:\nHao, Lizheng (2021): dat2.zip. figshare. 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"identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "asset:table:pmid:33552736:1", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:197575d80b21b2ef7fb3faaaa4f2006ed3deee210cdfae12b33c2cd4249c3353", "bytes": 2172, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[12]/table-wrap[1]#table-1", "version": null, "note": "Top 10 terms of BP, MF, CC.", "structure": {"pmcid": "PMC7825366", "section_index": 12, "section_title": "Identification and selection of the immunological TME related DEGs and GO analysis", "row_count": 31, "column_count": 4}, "table": {"label": "Table 1", "caption": "Top 10 terms of BP, MF, CC.", "rows": [["Category", "GO-ID", "GO-Term", "Adj P value"], ["MF", "GO0003823", "Antigen binding", "2.82E−29"], ["MF", "GO0005125", "Cytokine activity", "1.98E−12"], ["MF", "GO0004896", "Cytokine receptor activity", "5.95E−12"], ["MF", "GO0042287", "MHC protein binding", "3.85E−10"], ["MF", "GO0008009", "Chemokine activity", "4.74E−10"], ["MF", "GO0030246", "Carbohydrate binding", "1.33E−09"], ["MF", "GO0042379", "Chemokine receptor binding", "3.36E−09"], ["MF", "GO0005126", "Cytokine receptor binding", "4.14E−09"], ["MF", "GO0048020", "CCR chemokine receptor binding", "8.63E−09"], ["MF", "GO0034987", "Immunoglobulin receptor binding", "2.28E−08"], ["BP", "GO0002429", "Immune response-activating cell surface receptor signaling pathway", "1.94E−56"], ["BP", "GO0051249", "Regulation of lymphocyte activation", "1.94E−56"], ["BP", "GO0042110", "T cell activation", "1.58E−52"], ["BP", "GO0002460", "Adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains", "2.32E−44"], ["BP", "GO0050867", "Positive regulation of cell activation", "2.7E−44"], ["BP", "GO0002696", "Positive regulation of leukocyte activation", "1.07E−43"], ["BP", "GO0050863", "Regulation of T cell activation", "3.29E−42"], ["BP", "GO0007159", "Leukocyte cell–cell adhesion", "6.12E−41"], ["BP", "GO0070661", "Leukocyte proliferation", "6.89E−41"], ["BP", "GO0046651", "Lymphocyte proliferation", "1.23E−40"], ["CC", "GO0042101", "T cell receptor complex", "5.35E−54"], ["CC", "GO0098802", "Plasma membrane receptor complex", "3.06E−46"], ["CC", "GO0009897", "External side of plasma membrane", "1.4E−45"], ["CC", "GO0019814", "Immunoglobulin complex", "8.93E−35"], ["CC", "GO0042613", "MHC class II protein complex", "5.75E−12"], ["CC", "GO0070820", "Tertiary granule", "2.3E−09"], ["CC", "GO0042611", "MHC protein complex", "3.26E−09"], ["CC", "GO0001772", "Immunological synapse", "1.82E−08"], ["CC", "GO0042571", "Immunoglobulin complex, circulating", "1.58E−07"], ["CC", "GO0042581", "Specific granule", "7.85E−07"]], "row_count": 31, "column_count": 4, "numeric_cells": 60, "header_rows": 1, "locator": "section[12]/table-wrap[1]#table-1"}}, {"id": "asset:table:pmid:33552736:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:c8b2d1bd0c01fdc1215291a253152792a6450ca17076cae5f6efb9b50f4f1360", "bytes": 1839, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[18]/table-wrap[1]#table-2", "version": null, "note": "The biological functions of the coding genes.", "structure": {"pmcid": "PMC7825366", "section_index": 18, "section_title": "Discussion", "row_count": 12, "column_count": 2}, "table": {"label": "Table 2", "caption": "The biological functions of the coding genes.", "rows": [["Gene", "Immune-related functions"], ["CD70", "CD70 belongs to TNF ligand family and can enhance the generation of cytolytic T cells and induce proliferation of co-stimulated T cells (Keller et al., 2007; Kuka et al., 2013). The regulatory mechanisms for the CD70-CD27 pathway is critical for prognosis of cancer patients."], ["CXorf21", "CXorf21 is a mediator of the X-chromosome gene of systemic lupus erythematosus in female (Bentham et al., 2015; Harris et al., 2019b) and is expressed only in immune cell (Harris et al., 2019a)."], ["CD74", "CD74 expression serves as a prognostic factor in many cancers (Ekmekcioglu et al., 2016; Otterstrom et al., 2014; Ruvolo et al., 2019; Zeiner et al., 2015; Zeiner et al., 2018; Zhang et al., 2014)."], ["RUBCNL", "RUBCNL is a vertebrate-specific autophagy regulator (Cheng et al., 2017), and involves autophagy in NSCLC (Levy, Towers & Thorburn, 2017)."], ["BIRC3", "BIRC3 involves in the prognostication system in Chronic Lymphocytic Leukemia (Alhourani et al., 2016) and hepatocellular carcinoma patients undergoing curative resection (Fu et al., 2019)."], ["TESC", "TESC can reinforce the radio-resistant properties of NSCLC (Lee et al., 2018)."], ["INSL4", "Abnormal INSL4 signaling may act as a promising therapeutic target for LKB1-deficient NSCLC (Yang et al., 2018)."], ["HLA-DOB", "HLA-DOB are expressed in antigen presenting cells which is tightly linked with the immunity."], ["CIITA", "The vaccination with CIITA-tumour cells is constructed to facilitate anti-tumour cells to enhance the immune system (Accolla et al., 2019)."], ["STAP1", "No relevant report yet."], ["OBP2A", "No relevant report yet."]], "row_count": 12, "column_count": 2, "numeric_cells": 11, "header_rows": 1, "locator": "section[18]/table-wrap[1]#table-2"}}], "gaps": ["asset:data:geo:GSE68465 not downloaded", "asset:data:geo:GSE68465 licence not read"]}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "reordered", "quote": "“LASSO COX regression was applied to build the prediction model.”"}}, {"id": "method-2", "family": "network_analysis", "specific": "pathway_enrichment", "label": "Network / pathway analysis", "dsl_operations": ["pathway_enrich"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["edge_list"], "evidence": {"score": 0.8, "band": "high", "quote": "GO enrichment"}}, {"id": "method-3", "family": "diagnostic_evaluation", "specific": "roc", "label": "Diagnostic test evaluation", "dsl_operations": ["confusion_counts", "roc_curve", "sensitivity_specificity", "solve_confusion_matrix", "classification_metrics", "published_precision_envelope"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["reference_standard_and_test"], "evidence": {"score": 0.8, "band": "high", "quote": "ROC curve"}}], "targets": [], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. 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