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pmid:38873416

IL4I1: a novel molecular biomarker represents an inflamed tumor microenvironment and precisely predicts the molecular subtype and immunotherapy response of bladder cancer.

Xiangrong Peng · Chuan Liu · Li Zhang · Yin Chen · Lixin Mao · Shenglin Gao · Xiaokai Shi · Li Zuo

Frontiers in pharmacology · 2024 doi:10.3389/fphar.2024.1365683

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Experiment

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Data

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Analysis

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title
IL4I1: a novel molecular biomarker represents an inflamed tumor microenvironment and precisely predicts the molecular subtype and immunotherapy response of bladder cancer.
doi
10.3389/fphar.2024.1365683
pmid
38873416
authors array · 8 items
[0]
Xiangrong Peng
[1]
Chuan Liu
[2]
Li Zhang
[3]
Yin Chen
[4]
Lixin Mao
[5]
Shenglin Gao
[6]
Xiaokai Shi
[7]
Li Zuo
journal
Frontiers in pharmacology
year
2024
abstract
Introduction: IL4I1, also known as Interleukin-4-induced gene 1, is an enzyme that can modulate the immune system by acting as a L-amino acid oxidase. Nevertheless, a precise understanding of the correlation of IL4I1 with immunological features and immunotherapy efficacy in bladder cancer (BLCA) remains incomplete. Methods: We analyzed RNA sequencing data from the Cancer Genome Atlas (TCGA) to investigate the immune function and prognostic importance of IL4I1 across different cancer types. We further examined the TCGA-BLCA cohort for correlations between IL4I1 and various immunological characteristics of tumor microenvironment (TME), such as cancer immune cycle, immune cell infiltration, immune checkpoint expression and T cell inflamed score. Validation was conducted using two independent cohort, GSE48075 and E-MTAB-4321. Finally, RNA sequencing data from the IMvigor210 cohort and immunohistochemistry assays were employed to validate the predictive value of IL4I1 for the TME and immunotherapy efficacy. Results: In our findings, a positive correlation was observed between IL4I1 expression and immunomodulators expression, immune cell infiltration, the cancer immune cycle, and T cell inflamed score in BLCA, suggesting a significant link to the inflamed TME. In addition, studies have shown that IL4I1 elevated levels of individuals tend to be more performance for basal subtype and exhibit enhanced response rates to diverse treatment modalities, specifically immunotherapy. Clinical data from the IMvigor 210 cohort confirmed a higher rate of response to immunotherapy and better survival benefits in patients with high IL4I1 expression. Discussion: To summarize, our research showed that elevated IL4I1 levels are indicative of an inflamed TME, the basal subtype, and a more favorable response to various treatment methods, especially immune checkpoint blockade therapy in BLCA.
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Elevated IL4I1 expression indicates an inflamed bladder cancer tumor microenvironment, the basal molecular subtype, and a more favorable response to treatment, especially immune checkpoint blockade therapy.
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To summarize, our research showed that elevated IL4I1 levels are indicative of an inflamed TME, the basal subtype, and a more favorable response to various treatment methods, especially immune checkpoint blockade therapy in BLCA.
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pmid:38873416
parent_hash
sha256:4fb67e13214be58c4973e3e8e45c6f8ba1ec4e422343b15e263ba38b2b851f67
fork_of
null
gaps array · 11 items
[0]
asset:data:geo:E-MTAB-4321 licence not read
[1]
asset:data:geo:E-MTAB-4321 not downloaded
[2]
asset:data:geo:GSE48075 licence not read
[3]
asset:data:geo:GSE48075 not downloaded
[4]
asset:data:geo:GSE78220 licence not read
[5]
asset:data:geo:GSE78220 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 · 3 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
0.99
evidence array · 2 items
[0]
CA) remains incomplete. Methods: We analyzed RNA sequencing data from the Cancer Genome Atlas (TCGA) to
[1]
t cohort, GSE48075 and E-MTAB-4321. Finally, RNA sequencing data from the IMvigor210 cohort and immunohi
order_basis
paper_text_order:465
id
assay:1
[1] object · 11 fields
role
data_generation
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 2 items
[0]
quencing data from the IMvigor210 cohort and immunohistochemistry assays were employed to validate the predict
[1]
gies. (H) Validation by external cohorts and immunohistochemistry. Statistical analysis To evaluate difference
order_basis
paper_text_order:1021
id
assay:2
[2] 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]
The Pearson correlation analysis was utilized to quantify correlation.
order_basis
consumes_earlier_output
id
assay:3
Complete file
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Nevertheless, a precise understanding of the correlation of IL4I1 with immunological features and immunotherapy efficacy in bladder cancer (BLCA) remains incomplete. Methods: We analyzed RNA sequencing data from the Cancer Genome Atlas (TCGA) to investigate the immune function and prognostic importance of IL4I1 across different cancer types. We further examined the TCGA-BLCA cohort for correlations between IL4I1 and various immunological characteristics of tumor microenvironment (TME), such as cancer immune cycle, immune cell infiltration, immune checkpoint expression and T cell inflamed score. Validation was conducted using two independent cohort, GSE48075 and E-MTAB-4321. Finally, RNA sequencing data from the IMvigor210 cohort and immunohistochemistry assays were employed to validate the predictive value of IL4I1 for the TME and immunotherapy efficacy. Results: In our findings, a positive correlation was observed between IL4I1 expression and immunomodulators expression, immune cell infiltration, the cancer immune cycle, and T cell inflamed score in BLCA, suggesting a significant link to the inflamed TME. In addition, studies have shown that IL4I1 elevated levels of individuals tend to be more performance for basal subtype and exhibit enhanced response rates to diverse treatment modalities, specifically immunotherapy. Clinical data from the IMvigor 210 cohort confirmed a higher rate of response to immunotherapy and better survival benefits in patients with high IL4I1 expression. 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