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pmid:38552222

Role of CCR1/5/7 in hepatocellular carcinoma: a study on prognostic evaluation, molecular subtyping, and association with immune infiltration.

Huasheng Huang · Chenlu Lan · Yongguang Wei · Jusen Nong · Xiwen Liao · Xinping Ye · Ganlu Deng · Tao Peng · Xin Zhou

Aging · 2024 doi:10.18632/aging.205698

Paper

complete

Experiment

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Data

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Analysis

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title
Role of CCR1/5/7 in hepatocellular carcinoma: a study on prognostic evaluation, molecular subtyping, and association with immune infiltration.
doi
10.18632/aging.205698
pmid
38552222
authors array · 9 items
[0]
Huasheng Huang
[1]
Chenlu Lan
[2]
Yongguang Wei
[3]
Jusen Nong
[4]
Xiwen Liao
[5]
Xinping Ye
[6]
Ganlu Deng
[7]
Tao Peng
[8]
Xin Zhou
journal
Aging
year
2024
abstract
This study aims to assess the prognostic value of the C-C motif chemokine receptor (CCR) gene family in hepatocellular carcinoma (HCC) and its relationship with immune infiltration and molecular subtypes of HCC. The evaluation of the GSE14520 dataset and TCGA database confirmed the prognostic significance of CCR. Building upon the correlation between CCR1, CCR5, and CCR7 and favorable prognosis, we further validated the prognostic importance of CCR1, CCR5, and CCR7 in ICGC database and an independent cohort from Guangxi autonomous region. Then, we constructed a risk prognosis model. Additionally, we observed significant positive correlations between CCR1, CCR5, and CCR7 and the infiltration of B cells, T cells, and macrophages in HCC. Subsequently, we conducted CCK assays, Transwell assays, and colony formation assays to evaluate the molecular biological functions of CCR1, CCR5, and CCR7. These experiments further confirmed that upregulation of CCR1, CCR5, and CCR7 can individually inhibit the proliferation, migration, and stemness of HCC cells. By analyzing the relationship between expression levels and tumor mutation frequency, we discovered that patients with high CCR1 expression were more likely to be classified as non-proliferative HCC. Similar conclusions were observed for CCR5 and CCR7. The association of CCR1, CCR5, and CCR7 with the molecular subtypes of HCC suggests that they may serve as intermediary molecules linking immune status and molecular subtypes in HCC. In summary, CCR1, CCR5, and CCR7 have the potential to serve as prognostic biomarkers for HCC and regulate HCC progression by influencing immune cell infiltration.
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The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis.
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sections[18] "Statistical analysis" paragraph 2
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The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis.
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L).
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The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L).
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The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L).
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group_sizes_basis
null
platform
3921;571
taxon
Homo sapiens
title
Gene expression data of human hepatocellular carcinoma (HCC)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[0]
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complete
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method-1
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survival_analysis
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kaplan_meier
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Survival analysis
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survival_km
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time_to_event_with_censoring
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1
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verbatim
quote
The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis.
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method-2
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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[0]
time_to_event_with_censoring
evidence object · 3 fields
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0.8
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high
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Cox proportional hazards
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method-3
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survival_analysis
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log_rank_test
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Survival analysis
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[0]
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data_shapes array · 1 item
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time_to_event_with_censoring
evidence object · 3 fields
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0.8
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log-rank
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method-4
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diagnostic_evaluation
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Diagnostic test evaluation
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reference_standard_and_test
evidence object · 3 fields
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0.8
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high
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ROC analysis
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[0] object · 8 fields
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target-published-estimate
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claim-target-result
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classification_metrics
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p-value
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null
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complete
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The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold.
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capability object · 3 fields
state
complete
requirements array · 1 item
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capability_id
capability:computational_analysis
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gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
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state
complete
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R1
blocked_on
nothing:replicable_now
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method object · 5 fields
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true
required_operations array · 1 item
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survival_km
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: kaplan_meier.
capability object · 4 fields
tier
R1
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capability:computational_analysis
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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
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R1
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GSE14520
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[0]
GSE14520
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[0]
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
basis
The paper names GSE14520 in GEO database 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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survival_km
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[1]
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run_analysis
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data:geo:GSE14520
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review object · 5 fields
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
provider_family
minimax
read_at
2026-11-01T19:14:06Z
independence
single_reader
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verbatim
availability
verbatim
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5
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14219
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2370
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128
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[0] object · 4 fields
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extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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absent
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not_run
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null
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provenance object · 7 fields
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pmid:38552222
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paper
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pmid:38552222
[1] object · 3 fields
id
source:pmid:38552222
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manuscript
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PMID 38552222 full text
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id
data:geo:GSE14520
type
dataset
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GEO GSE14520
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
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classification
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pmid:38552222
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paper
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pmid:38552222
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source:pmid:38552222
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manuscript
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PMID 38552222 full text
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data:geo:GSE14520
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dataset
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GEO GSE14520
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agent:corpus-assay-engine
[1] object · 4 fields
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activity-read-38552222
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agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE14520
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accession_resolution
used array · 1 item
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agent:corpus-assay-engine
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[0] object · 3 fields
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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f2132e96ae6c7a4e
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The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis.
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analysis_only
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38552222", "kind": "science-record", "revision": 4, "content_hash": "sha256:f5b4338be2fe3a08d8fb436691a9d59408290b87366fff2815e5e220788bd6ea", "created_at": "2026-11-01T19:20:31Z", "updated_at": "2026-11-01T22:54:01Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Role of CCR1/5/7 in hepatocellular carcinoma: a study on prognostic evaluation, molecular subtyping, and association with immune infiltration.", "doi": "10.18632/aging.205698", "pmid": "38552222", "authors": ["Huasheng Huang", "Chenlu Lan", "Yongguang Wei", "Jusen Nong", "Xiwen Liao", "Xinping Ye", "Ganlu Deng", "Tao Peng", "Xin Zhou"], "journal": "Aging", "year": 2024, "abstract": "This study aims to assess the prognostic value of the C-C motif chemokine receptor (CCR) gene family in hepatocellular carcinoma (HCC) and its relationship with immune infiltration and molecular subtypes of HCC. The evaluation of the GSE14520 dataset and TCGA database confirmed the prognostic significance of CCR. Building upon the correlation between CCR1, CCR5, and CCR7 and favorable prognosis, we further validated the prognostic importance of CCR1, CCR5, and CCR7 in ICGC database and an independent cohort from Guangxi autonomous region. Then, we constructed a risk prognosis model. Additionally, we observed significant positive correlations between CCR1, CCR5, and CCR7 and the infiltration of B cells, T cells, and macrophages in HCC. Subsequently, we conducted CCK assays, Transwell assays, and colony formation assays to evaluate the molecular biological functions of CCR1, CCR5, and CCR7. These experiments further confirmed that upregulation of CCR1, CCR5, and CCR7 can individually inhibit the proliferation, migration, and stemness of HCC cells. By analyzing the relationship between expression levels and tumor mutation frequency, we discovered that patients with high CCR1 expression were more likely to be classified as non-proliferative HCC. Similar conclusions were observed for CCR5 and CCR7. The association of CCR1, CCR5, and CCR7 with the molecular subtypes of HCC suggests that they may serve as intermediary molecules linking immune status and molecular subtypes in HCC. In summary, CCR1, CCR5, and CCR7 have the potential to serve as prognostic biomarkers for HCC and regulate HCC progression by influencing immune cell infiltration.", "claims": [{"id": "claim-method", "statement": "The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38552222", "locator": "sections[18] \"Statistical analysis\" paragraph 2", "quote": "The Kaplan-Meier method along with the log-rank test and Cox proportional hazards model was respectively applied for the survival analysis."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38552222", "locator": "sections[19] \"Availability of data and material\" paragraph 2", "quote": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L).", "kind": "quantitative", "target": {"value": 0.025, "unit": "p-value", "tolerance": null, "source": "The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L)."}, "evidence": [{"asset": "source:pmid:38552222", "locator": "sections[25] \"Nomogram and prognostic signature\" paragraph 6", "quote": "The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The difference between the high and low risk groups in OS was statistically significant (P=0.025, Figure 4L).", "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:38552222"], "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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