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pmid:35117761

LncRNA FENDRR-mediated tumor suppression and tumor-immune microenvironment changes in non-small cell lung cancer.

Hongyu Pan · Tao Yu · Lei Sun · Wenjun Chai · Xiaoli Liu · Mingxia Yan

Translational cancer research · 2020 doi:10.21037/tcr-20-2147

Paper

complete

Experiment

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Data

partial

Analysis

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title
LncRNA FENDRR-mediated tumor suppression and tumor-immune microenvironment changes in non-small cell lung cancer.
doi
10.21037/tcr-20-2147
pmid
35117761
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[0]
Hongyu Pan
[1]
Tao Yu
[2]
Lei Sun
[3]
Wenjun Chai
[4]
Xiaoli Liu
[5]
Mingxia Yan
journal
Translational cancer research
year
2020
abstract
BACKGROUND: Long noncoding RNAs (lncRNAs) play a key role in the development and progression of many cancer types, including lung cancer. The objective of this study is to examine the function and molecular mechanism of lncRNAs involved in non-small cell lung cancer (NSCLC). METHODS: First, 7 lung cancer-related differentially expressed LncRNAs were screened from 2 genomic profiling datasets. Of these lncRNAs, FOXF1 adjacent noncoding developmental regulatory RNA (FENDRR) was found to be the only one that was both significantly down-regulated in the patients with advanced pathology and negatively correlated with prognosis. Thus, lncRNA FENDRR was further studied in this project. Clinical correlation analysis was further conducted in the GSE30219 dataset and 73 paired lung cancer and noncancerous tissues stored in our lab; Subsequently, we evaluated FENDRR coding potential with the Phylogenetic Codon Substitution Frequencies (PhyloCSF), Coding-Potential Assessment Tool (CPAT), and Coding Potential Calculator (CPC) online analytical tool. The cell growth ability was measured by CCK8 assay and clonogenicity assay, the metastatic capacities were evaluated using Transwell migration and invasion assays. Mechanistically, we analyzed the correlation of FENDRR function in NSCLC with immune response by utilizing The Cancer Genome Atlas (TCGA) data. RESULTS: Results indicated a negative clinical correlation of FENDRR. Coding potential analysis showed FENDRR as a noncoding RNA. Elevated expression of FENDRR led to cell growth arrest, inhibition of proliferative ability, declined migration and invasion potential of NSCLC cells in vitro. Mechanistically, we discovered that FENDRR expression might be involved in aberrant immune response regulation. CONCLUSIONS: Taken together, our results provide a greater understanding of lncRNA FENDRR as a tumor suppressor with respect to tumor-immune interactions in NSCLC.
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Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM).
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Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM).
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Data Sharing Statement: Available at http://dx.doi.org/10.21037/tcr-20-2147
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Taken together, our results provide a greater understanding of lncRNA FENDRR as a tumor suppressor with respect to tumor-immune interactions in NSCLC.
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sample_count
307
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
"Off-context" gene expression in lung cancer identifies a group of metastatic-prone tumors
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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gaps array · 6 items
[0]
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[2]
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[3]
asset:data:geo:GSE13213 licence not read
[4]
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[5]
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state
complete
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id
method-1
family
survival_analysis
specific
log_rank_test
label
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[0]
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parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
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verbatim
quote
Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM).
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gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
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[0]
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
R1
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nothing:replicable_now
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method object · 5 fields
tier
R1
expressible
true
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logrank_test
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: log_rank_test.
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]
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[1]
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GSE30219
resolved_accessions array · 3 items
[0]
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GSE30219
statements array · 1 item
[0]
Data Sharing Statement: Available at http://dx.doi.org/10.21037/tcr-20-2147
basis
The paper names GSE102287, GSE13213, GSE30219 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
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[0]
logrank_test
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[0]
source:pmid:35117761
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data:geo:GSE102287
steps array · 1 item
[0]
run_analysis
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[0]
data:geo:GSE102287
gaps array · 0 items
review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T17:32:44Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
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1835
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id
extraction
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complete
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state
absent
status
not_run
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null
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[0]
execution.not_run
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entities array · 3 items
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id
pmid:35117761
type
paper
label
pmid:35117761
[1] object · 3 fields
id
source:pmid:35117761
type
manuscript
label
PMID 35117761 full text
[2] object · 3 fields
id
data:geo:GSE102287
type
dataset
label
GEO GSE102287
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[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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type
paper
label
pmid:35117761
[1] object · 3 fields
id
source:pmid:35117761
type
manuscript
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PMID 35117761 full text
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id
data:geo:GSE102287
type
dataset
label
GEO GSE102287
agent
agent:corpus-assay-engine
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id
activity-read-35117761
type
extraction
used array · 1 item
[0]
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agent
agent:minimax-reader
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type
accession_resolution
used array · 1 item
[0]
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agent:corpus-assay-engine
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agent:corpus-assay-engine
type
software
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id
agent:minimax-reader
type
software
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lineage object · 4 fields
parent_id
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sha256:3fa3be8c855efe310f0b9f35ca9cd2f8eb6a23fe321f1e3b3524953e0bb1b6d7
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[0] object · 11 fields
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data_generation
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apoptosis_assay
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99e1195c7d6f
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evidence array · 1 item
[0]
ool. The cell growth ability was measured by CCK8 assay and clonogenicity assay, the metastati
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paper_text_order:1162
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assay:1
[1] object · 11 fields
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data_generation
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evidence array · 2 items
[0]
ckaging of lentivirus containing FENDRR. All cell lines were maintained in Dulbecco Modified Eagle’s Medium (DMEM) (
[1]
line (ATCC, Cat# CRL-5803, RRID:CVCL_0060), A549 cell line (ATCC, Cat# CCL-185, RRID:CVCL_002
order_basis
paper_text_order:2811
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assay:2
[2] object · 11 fields
role
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f2132e96ae6c7a4e
evidence array · 1 item
[0]
Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35117761", "kind": "science-record", "revision": 3, "content_hash": "sha256:e20dca3f8f42b0d0a7e8b53a68fa5ffe58c582ae390536a2e1791a11e6519077", "created_at": "2026-11-01T17:36:52Z", "updated_at": "2026-11-01T21:27:09Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "LncRNA FENDRR-mediated tumor suppression and tumor-immune microenvironment changes in non-small cell lung cancer.", "doi": "10.21037/tcr-20-2147", "pmid": "35117761", "authors": ["Hongyu Pan", "Tao Yu", "Lei Sun", "Wenjun Chai", "Xiaoli Liu", "Mingxia Yan"], "journal": "Translational cancer research", "year": 2020, "abstract": "BACKGROUND: Long noncoding RNAs (lncRNAs) play a key role in the development and progression of many cancer types, including lung cancer. The objective of this study is to examine the function and molecular mechanism of lncRNAs involved in non-small cell lung cancer (NSCLC).\nMETHODS: First, 7 lung cancer-related differentially expressed LncRNAs were screened from 2 genomic profiling datasets. Of these lncRNAs, FOXF1 adjacent noncoding developmental regulatory RNA (FENDRR) was found to be the only one that was both significantly down-regulated in the patients with advanced pathology and negatively correlated with prognosis. Thus, lncRNA FENDRR was further studied in this project. Clinical correlation analysis was further conducted in the GSE30219 dataset and 73 paired lung cancer and noncancerous tissues stored in our lab; Subsequently, we evaluated FENDRR coding potential with the Phylogenetic Codon Substitution Frequencies (PhyloCSF), Coding-Potential Assessment Tool (CPAT), and Coding Potential Calculator (CPC) online analytical tool. The cell growth ability was measured by CCK8 assay and clonogenicity assay, the metastatic capacities were evaluated using Transwell migration and invasion assays. Mechanistically, we analyzed the correlation of FENDRR function in NSCLC with immune response by utilizing The Cancer Genome Atlas (TCGA) data.\nRESULTS: Results indicated a negative clinical correlation of FENDRR. Coding potential analysis showed FENDRR as a noncoding RNA. Elevated expression of FENDRR led to cell growth arrest, inhibition of proliferative ability, declined migration and invasion potential of NSCLC cells in vitro. Mechanistically, we discovered that FENDRR expression might be involved in aberrant immune response regulation.\nCONCLUSIONS: Taken together, our results provide a greater understanding of lncRNA FENDRR as a tumor suppressor with respect to tumor-immune interactions in NSCLC.", "claims": [{"id": "claim-method", "statement": "Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35117761", "locator": "sections[11] \"Statistical analysis\" paragraph 2", "quote": "Two-tailed Student’s t-test was used to determine differences between 2 means. The log-rank Cox test was conducted to assess the difference in survival with the data being presented as the mean ± standard error of the mean (SEM)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data Sharing Statement: Available at http://dx.doi.org/10.21037/tcr-20-2147", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35117761", "locator": "sections[20] \"fn-group\" paragraph 1", "quote": "Data Sharing Statement: Available at http://dx.doi.org/10.21037/tcr-20-2147"}], "state": "complete"}, {"id": "claim-target-result", "statement": "lncRNA FENDRR acts as a tumor suppressor associated with tumor-immune interactions in NSCLC.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35117761", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Taken together, our results provide a greater understanding of lncRNA FENDRR as a tumor suppressor with respect to tumor-immune interactions in NSCLC."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "lncRNA FENDRR acts as a tumor suppressor associated with tumor-immune interactions in NSCLC.", "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:35117761"], "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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