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pmid:34374416

Immune implication of an autophagy-related prognostic signature in uveal melanoma.

Samuel Chuah · Valerie Chew

Bioscience reports · 2021 doi:10.1042/BSR20211098

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:34374416
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title
Immune implication of an autophagy-related prognostic signature in uveal melanoma.
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10.1042/BSR20211098
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34374416
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Samuel Chuah
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Valerie Chew
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Bioscience reports
year
2021
abstract
Uveal Melanoma (UM) is a rare cancer deriving from melanocytes within the uvea. It has a high rate of metastasis, especially to the liver, and a poor prognosis thereafter. Autophagy, an intracellular programmed digestive process, has been associated with the development and progression of cancers, with controversial pro- and anti-tumour roles. Although previous studies have been conducted on autophagy-related genes (ARGs) in various cancer types, its role in UM requires a deeper understanding for improved diagnosis and development of novel therapeutics. In the present study, Zheng et al. used univariate Cox regression followed by least absolute shrinkage and selection operator (Lasso) regression to identify a robust 9-ARG signature prognostic of survival in a total of 230 patients with UM. The authors used the Cancer Genome Atlas (TCGA) UM cohort as a training cohort (n=80) to identify the signature and validated it in another four independent cohorts of 150 UM patients from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976). This 9-ARG signature was also significantly associated with the enrichment of cancer hallmarks, including angiogenesis, IL6-KJAK-STAT3 signalling, reactive oxygen species pathway and oxidative phosphorylation. More importantly, this signature is associated with immune-related functional pathways and immune cell infiltration. Thus, this 9-ARG signature predicts prognosis and provides deeper insights into the immune mechanisms in UM, with potential implications for future immunotherapy.
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Using the TCGA cohort (n=80) as the training cohort, univariate Cox regression analysis narrowed this list down to 133 ARGs, which were associated with overall survival (OS). From these ARGs, a final prognostic signature of 9-ARGs was then established using Lasso Cox regression.
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sections[2] "Identification of an ARGs signature predictive of UM prognosis" paragraph 2
quote
Using the TCGA cohort (n=80) as the training cohort, univariate Cox regression analysis narrowed this list down to 133 ARGs, which were associated with overall survival (OS). From these ARGs, a final prognostic signature of 9-ARGs was then established using Lasso Cox regression.
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Zheng et al. [17] first obtained bulk RNAseq data from five UM cohorts: The Cancer Genome Atlas (TCGA) cohort, and four others from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976), and identified 423 ARGs which were expressed across all the cohorts.
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Zheng et al. [17] first obtained bulk RNAseq data from five UM cohorts: The Cancer Genome Atlas (TCGA) cohort, and four others from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976), and identified 423 ARGs which were expressed across all the cohorts.
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[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:34374416
parent_hash
sha256:0b890fd52adeaed26a9032a0811ecbae364b8102fcf673a752ae7c9b13052ba2
fork_of
null
gaps array · 12 items
[0]
asset:data:geo:GSE22138 licence not read
[1]
asset:data:geo:GSE22138 not downloaded
[2]
asset:data:geo:GSE27831 licence not read
[3]
asset:data:geo:GSE27831 not downloaded
[4]
asset:data:geo:GSE44295 licence not read
[5]
asset:data:geo:GSE44295 not downloaded
[6]
asset:data:geo:GSE84976 licence not read
[7]
asset:data:geo:GSE84976 not downloaded
[8]
execution.not_run
[9]
review.human_critique
[10]
review.independent_reader
[11]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Using the TCGA cohort (n=80) as the training cohort, univariate Cox regression analysis narrowed this list down to 133 ARGs, which were associated with overall survival (OS). From these ARGs, a final prognostic signature of 9-ARGs was then established using Lasso Cox regression.
order_basis
analysis_only
id
assay:1
Complete file
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Autophagy, an intracellular programmed digestive process, has been associated with the development and progression of cancers, with controversial pro- and anti-tumour roles. Although previous studies have been conducted on autophagy-related genes (ARGs) in various cancer types, its role in UM requires a deeper understanding for improved diagnosis and development of novel therapeutics. In the present study, Zheng et al. used univariate Cox regression followed by least absolute shrinkage and selection operator (Lasso) regression to identify a robust 9-ARG signature prognostic of survival in a total of 230 patients with UM. The authors used the Cancer Genome Atlas (TCGA) UM cohort as a training cohort (n=80) to identify the signature and validated it in another four independent cohorts of 150 UM patients from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976). This 9-ARG signature was also significantly associated with the enrichment of cancer hallmarks, including angiogenesis, IL6-KJAK-STAT3 signalling, reactive oxygen species pathway and oxidative phosphorylation. More importantly, this signature is associated with immune-related functional pathways and immune cell infiltration. Thus, this 9-ARG signature predicts prognosis and provides deeper insights into the immune mechanisms in UM, with potential implications for future immunotherapy.", "claims": [{"id": "claim-method", "statement": "Using the TCGA cohort (n=80) as the training cohort, univariate Cox regression analysis narrowed this list down to 133 ARGs, which were associated with overall survival (OS). 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[17] first obtained bulk RNAseq data from five UM cohorts: The Cancer Genome Atlas (TCGA) cohort, and four others from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976), and identified 423 ARGs which were expressed across all the cohorts.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34374416", "locator": "sections[2] \"Identification of an ARGs signature predictive of UM prognosis\" paragraph 2", "quote": "Zheng et al. [17] first obtained bulk RNAseq data from five UM cohorts: The Cancer Genome Atlas (TCGA) cohort, and four others from the Gene Expression Omnibus (GEO) repository (GSE22138, GSE27831, GSE44295 and GSE84976), and identified 423 ARGs which were expressed across all the cohorts."}], "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:34374416"], "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:GSE22138"], "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:GSE22138"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34374416", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1042/BSR20211098", "sha256": "sha256:64ffb85c91fa7a075af0ddf48ef739da24167eb393f6c2a0fb57b196d85f4b8f", "bytes": 12410, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1042/BSR20211098", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC8380919", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE22138", "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=GSE22138", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE22138", "version": null, "note": "Zheng et al. 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