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pmid:38957390

Identification of anoikis-related gene signatures and construction of the prognosis model in prostate cancer.

Wanying Kang · Chen Ye · Yunyun Yang · Yan-Ru Lou · Mingyi Zhao · Zhuo Wang · Yuan Gao

Frontiers in pharmacology · 2024 doi:10.3389/fphar.2024.1383304

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title
Identification of anoikis-related gene signatures and construction of the prognosis model in prostate cancer.
doi
10.3389/fphar.2024.1383304
pmid
38957390
authors array · 7 items
[0]
Wanying Kang
[1]
Chen Ye
[2]
Yunyun Yang
[3]
Yan-Ru Lou
[4]
Mingyi Zhao
[5]
Zhuo Wang
[6]
Yuan Gao
journal
Frontiers in pharmacology
year
2024
abstract
Background: One of the primary reasons for tumor invasion and metastasis is anoikis resistance. Biochemical recurrence (BCR) of prostate cancer (PCa) serves as a harbinger of its distant metastasis. However, the role of anoikis in PCa biochemical recurrence has not been fully elucidated. Methods: Differential expression analysis was used to identify anoikis-related genes based on the TCGA and GeneCards databases. Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses. Moreover, Gene Expression Omnibus datasets (GSE70770 and GSE46602) were applied as validation cohorts. Gene Ontology, KEGG and GSVA were utilized to explore biological pathways and molecular mechanisms. Further, immune profiles were assessed using CIBERSORT, ssGSEA, and TIDE, while anti-cancer drugs sensitivity was analyzed by GDSC database. In addition, gene expressions in the model were examined using online databases (Human Protein Atlas and Tumor Immune Single-Cell Hub). Results: 113 differentially expressed anoikis-related genes were found. Four genes (EEF1A2, RET, FOSL1, PCA3) were selected for constructing a prognostic model. Using the findings from the Cox regression analysis, we grouped patients into groups of high and low risk. The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897. Moreover, larger percentage of immune infiltration of memory B cells, CD8 Tcells, neutrophils, and M1 macrophages were observed in the high-risk group than those in the low-risk group, whereas the percentage of activated mast cells and dendritic cells in the high-risk group were lower. An increased TIDE score was founded in the high-risk group, suggesting reduced effectiveness of ICI therapy. Additionally, the IC50 results for chemotherapy drugs indicated that the low-risk group was more sensitive to most of the drugs. Finally, the genes EEF1A2, RET, and FOSL1 were expressed in PCa cases based on HPA website. The TISCH database suggested that these four ARGs might contribute to the tumor microenvironment of PCa. Conclusion: We created a risk model utilizing four ARGs that effectively predicts the risk of BCR in PCa patients. This study lays the groundwork for risk stratification and predicting survival outcomes in PCa patients with BCR.
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Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses.
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Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
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The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.
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The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.
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The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.
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The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.
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Apply the paper's statistical method to the resolved series and compare the result with the published target.
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GSM1848429
[387]
GSM1848430
[388]
GSM1848431
[389]
GSM1848432
[390]
GSM1848433
[391]
GSM1848435
[392]
GSM1848436
[393]
GSM1848437
[394]
GSM1848438
[395]
GSM1848439
[396]
GSM1848440
[397]
GSM1848441
[398]
GSM1848442
[399]
GSM1848443
[400]
GSM1848444
[401]
GSM1848445
[402]
GSM1848446
[403]
GSM1848447
[404]
GSM1848448
[405]
GSM1848449
[406]
GSM1848450
[407]
GSM1848451
[408]
GSM1848452
[409]
GSM1848453
[410]
GSM1848454
[411]
GSM1848455
[412]
GSM1848456
[413]
GSM1848457
[414]
GSM1848458
[415]
GSM1848459
[416]
GSM1848460
[417]
GSM1848461
[418]
GSM1848462
[419]
GSM1848463
[420]
GSM1848464
[421]
GSM1848465
[422]
GSM1848466
[423]
GSM1848467
[424]
GSM1848468
[425]
GSM1848469
[426]
GSM1848470
[427]
GSM1848471
[428]
GSM1848472
[429]
GSM1848473
[430]
GSM1848474
[431]
GSM1848475
[432]
GSM1848476
[433]
GSM1848477
[434]
GSM1848478
[435]
GSM1848479
[436]
GSM1848480
[437]
GSM1848481
[438]
GSM1848482
[439]
GSM1848483
[440]
GSM1848484
[441]
GSM1848485
[442]
GSM1848486
[443]
GSM1848487
[444]
GSM1848488
[445]
GSM1848489
[446]
GSM1848490
[447]
GSM1848491
[448]
GSM1848492
[449]
GSM1848493
[450]
GSM1848494
[451]
GSM1848495
[452]
GSM1848496
[453]
GSM1848497
[454]
GSM1848498
[455]
GSM1848499
[456]
GSM1848500
[457]
GSM1848501
[458]
GSM1848502
[459]
GSM1848503
[460]
GSM1848504
[461]
GSM1848505
[462]
GSM1848506
[463]
GSM1848507
[464]
GSM1848508
[465]
GSM1848509
[466]
GSM1848510
[467]
GSM1848511
[468]
GSM1848512
[469]
GSM1848513
[470]
GSM1848514
[471]
GSM1848515
[472]
GSM1848516
[473]
GSM1848517
[474]
GSM1848518
[475]
GSM1848519
[476]
GSM1848520
[477]
GSM1848521
[478]
GSM1848522
[479]
GSM1848523
[480]
GSM1848524
[481]
GSM1848525
[482]
GSM1848526
[483]
GSM1848527
[484]
GSM1848528
[485]
GSM1848529
[486]
GSM1848530
[487]
GSM1848531
[488]
GSM1848532
[489]
GSM1848533
[490]
GSM1848534
[491]
GSM1848535
[492]
GSM1848536
[493]
GSM1848537
[494]
GSM1848538
[495]
GSM1848539
[496]
GSM1848540
[497]
GSM1848541
[498]
GSM1848542
[499]
GSM1848543
[500]
GSM1848544
[501]
GSM1848545
[502]
GSM1848546
[503]
GSM1848547
[504]
GSM1848548
[505]
GSM1848549
[506]
GSM1848550
[507]
GSM1848551
[508]
GSM1848552
[509]
GSM1848553
[510]
GSM1848554
[511]
GSM1848555
[512]
GSM1848556
[513]
GSM1848557
[514]
GSM1848558
[515]
GSM1848559
[516]
GSM1848560
[517]
GSM1848561
[518]
GSM1848562
[519]
GSM1848563
[520]
GSM1848564
[521]
GSM1848565
[522]
GSM1848566
[523]
GSM1848567
[524]
GSM1848568
[525]
GSM1848569
[526]
GSM1848570
[527]
GSM1848571
[528]
GSM1848572
[529]
GSM1848573
[530]
GSM1848574
[531]
GSM1848575
[532]
GSM1848576
[533]
GSM1848577
[534]
GSM1848578
[535]
GSM1848579
[536]
GSM1848580
[537]
GSM1848581
[538]
GSM1848582
[539]
GSM1848583
[540]
GSM1848584
[541]
GSM1848585
[542]
GSM1848586
[543]
GSM1848587
[544]
GSM1848588
[545]
GSM1848589
[546]
GSM1848590
[547]
GSM1848591
[548]
GSM1848592
[549]
GSM1848593
[550]
GSM1848594
[551]
GSM1848595
[552]
GSM1848596
[553]
GSM1848597
[554]
GSM1848598
[555]
GSM1848599
[556]
GSM1848600
[557]
GSM1848601
[558]
GSM1848602
[559]
GSM1848603
[560]
GSM1848604
[561]
GSM1848605
[562]
GSM1848606
[563]
GSM1848607
[564]
GSM1848608
[565]
GSM1848609
[566]
GSM1848611
[567]
GSM1848612
[568]
GSM1848613
[569]
GSM1848614
[570]
GSM1848615
[571]
GSM1848616
[572]
GSM1848617
[573]
GSM1848618
[574]
GSM1848619
[575]
GSM1848620
[576]
GSM1848621
[577]
GSM1848622
[578]
GSM1848623
[579]
GSM1848624
[580]
GSM1848625
[581]
GSM1848626
[582]
GSM1848627
[583]
GSM1848628
[584]
GSM1848629
[585]
GSM1848630
[586]
GSM1848631
[587]
GSM1848632
[588]
GSM1848633
[589]
GSM1848634
[590]
GSM1848635
[591]
GSM1848636
[592]
GSM1848637
[593]
GSM1880733
[594]
GSM1880734
[595]
GSM1880735
[596]
GSM1880736
[597]
GSM1880737
[598]
GSM1880738
[599]
GSM1880739
[600]
GSM1880740
[601]
GSM1880741
[602]
GSM1880742
[603]
GSM1880743
[604]
GSM1880744
[605]
GSM1880745
[606]
GSM1880746
[607]
GSM1880747
[608]
GSM1880748
[609]
GSM1880749
[610]
GSM1880750
[611]
GSM1880751
[612]
GSM1880752
[613]
GSM1880753
[614]
GSM1880754
[615]
GSM1880755
[616]
GSM1880756
[617]
GSM1880757
[618]
GSM1880758
[619]
GSM1880759
[620]
GSM1880760
[621]
GSM1880761
[622]
GSM1880762
[623]
GSM1880763
[624]
GSM1880764
[625]
GSM1880765
[626]
GSM1880766
[627]
GSM1880767
[628]
GSM1884737
[629]
GSM1884739
[630]
GSM1884740
[631]
GSM1884742
[632]
GSM1884744
[633]
GSM1884745
[634]
GSM1884747
[635]
GSM1884748
[636]
GSM1884750
[637]
GSM1884752
[638]
GSM1884753
[639]
GSM1884755
[640]
GSM1884756
[641]
GSM1884758
[642]
GSM1884760
[643]
GSM1884761
[644]
GSM1884763
[645]
GSM1884765
[646]
GSM1884766
[647]
GSM1884768
[648]
GSM1884769
[649]
GSM1884771
[650]
GSM1884772
[651]
GSM1884773
[652]
GSM1884774
[653]
GSM1884775
[654]
GSM1884776
[655]
GSM1884777
[656]
GSM1884778
[657]
GSM1884779
[658]
GSM1884780
[659]
GSM1884781
[660]
GSM1884782
[661]
GSM1884783
[662]
GSM1884784
[663]
GSM1884785
[664]
GSM1884786
[665]
GSM1884787
[666]
GSM1884788
[667]
GSM1884789
[668]
GSM1884790
[669]
GSM1884791
[670]
GSM1884792
[671]
GSM1884793
[672]
GSM1884794
[673]
GSM1884795
[674]
GSM1884796
[675]
GSM1884797
[676]
GSM1884798
[677]
GSM1884799
[678]
GSM1884800
[679]
GSM1884801
[680]
GSM1884802
[681]
GSM1884803
[682]
GSM1884804
[683]
GSM1884805
[684]
GSM1884806
[685]
GSM1884807
[686]
GSM1884808
[687]
GSM1884809
[688]
GSM1884810
[689]
GSM1884811
[690]
GSM1884812
[691]
GSM1884813
[692]
GSM1884814
[693]
GSM1884815
[694]
GSM1884816
[695]
GSM1884817
[696]
GSM1884818
[697]
GSM1884819
[698]
GSM1884820
[699]
GSM1884821
[700]
GSM1884822
[701]
GSM1884823
[702]
GSM1884824
[703]
GSM1884825
[704]
GSM1884826
[705]
GSM1884827
[706]
GSM1884828
[707]
GSM1884829
[708]
GSM1884830
[709]
GSM1884831
[710]
GSM1884832
[711]
GSM1884833
[712]
GSM1884834
[713]
GSM1884835
[714]
GSM1884836
[715]
GSM1884837
[716]
GSM1884838
[717]
GSM1884839
[718]
GSM1884840
[719]
GSM1884841
[720]
GSM1884842
[721]
GSM1884843
[722]
GSM1884844
[723]
GSM1884845
[724]
GSM1884846
[725]
GSM1884847
[726]
GSM1884848
[727]
GSM1884849
[728]
GSM1884850
[729]
GSM1884851
[730]
GSM1884852
[731]
GSM1884853
[732]
GSM1884854
[733]
GSM1884855
[734]
GSM1884856
[735]
GSM1884857
[736]
GSM1884858
[737]
GSM1884859
[738]
GSM1884860
[739]
GSM1884861
[740]
GSM1884862
[741]
GSM1884863
[742]
GSM1884864
[743]
GSM1884865
[744]
GSM1884866
[745]
GSM1884867
[746]
GSM1884868
[747]
GSM1884869
[748]
GSM1884870
[749]
GSM1884871
[750]
GSM1884872
[751]
GSM1884873
[752]
GSM1884874
[753]
GSM1884875
[754]
GSM1884876
[755]
GSM1884877
[756]
GSM1884878
[757]
GSM1884879
[758]
GSM1884880
[759]
GSM1884881
[760]
GSM1884882
[761]
GSM1884883
[762]
GSM1884884
[763]
GSM1884885
[764]
GSM1884886
[765]
GSM1884887
[766]
GSM1884888
[767]
GSM1884889
[768]
GSM1884890
[769]
GSM1884891
[770]
GSM1884892
[771]
GSM1884893
[772]
GSM1884894
[773]
GSM1884895
[774]
GSM1884896
[775]
GSM1884897
[776]
GSM1884898
[777]
GSM1884899
[778]
GSM1884900
[779]
GSM1884901
[780]
GSM1884902
[781]
GSM1884903
[782]
GSM1884904
[783]
GSM1884905
[784]
GSM1884906
[785]
GSM1884907
[786]
GSM1884908
[787]
GSM1884909
[788]
GSM1884910
[789]
GSM1884911
[790]
GSM1884912
[791]
GSM1884913
[792]
GSM1884914
[793]
GSM1884915
[794]
GSM1884916
[795]
GSM1884917
[796]
GSM1884918
[797]
GSM1884919
[798]
GSM1884920
[799]
GSM1884921
[800]
GSM1884922
[801]
GSM1884923
[802]
GSM1884924
[803]
GSM1884925
[804]
GSM1884926
[805]
GSM1884927
[806]
GSM1884928
[807]
GSM1884929
sample_count
808
group_sizes
null
group_sizes_basis
null
platform
16104;6801;20641;10558
taxon
Homo sapiens
title
Prostate cancer stratification using molecular profiles
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 4 items
[0]
asset:data:geo:GSE46602 not downloaded
[1]
asset:data:geo:GSE46602 licence not read
[2]
asset:data:geo:GSE70770 not downloaded
[3]
asset:data:geo:GSE70770 licence not read
analysis object · 4 fields
state
partial
methods array · 7 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
verbatim
quote
Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses.
[1] object · 10 fields
id
method-2
family
group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[2] object · 10 fields
id
method-3
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
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
0.8
band
high
quote
Kaplan-Meier
[3] object · 10 fields
id
method-4
family
survival_analysis
specific
log_rank_test
label
Survival analysis
dsl_operations array · 1 item
[0]
logrank_test
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
0.8
band
high
quote
log-rank
[4] object · 10 fields
id
method-5
family
principal_component_analysis
specific
pca
label
Principal component analysis
dsl_operations array · 1 item
[0]
pca_fit
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
wide_numeric_matrix
evidence object · 3 fields
score
0.7
band
medium
quote
PCA
[5] object · 10 fields
id
method-6
family
correlation_analysis
specific
spearman
label
Correlation analysis
dsl_operations array · 1 item
[0]
spearman_rho
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
score
0.8
band
high
quote
Spearman correlation
[6] object · 10 fields
id
method-7
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
targets array · 1 item
[0] object · 8 fields
id
target-published-estimate
claim_id
claim-target-result
operation
cox_ph
unit
auc
tolerance
null
state
complete
note
The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none.
gaps array · 1 item
[0]
method.reader_differs_from_extractor
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 · 2 items
[0]
GSE70770
[1]
GSE46602
resolved_accessions array · 2 items
[0]
GSE70770
[1]
GSE46602
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
basis
The paper names GSE70770, GSE46602 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 · 2 items
[0]
source:pmid:38957390
[1]
data:geo:GSE46602
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:GSE46602
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
2026-11-01T19:22:53Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
18663
completion_tokens
1199
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
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:38957390
type
paper
label
pmid:38957390
[1] object · 3 fields
id
source:pmid:38957390
type
manuscript
label
PMID 38957390 full text
[2] object · 3 fields
id
data:geo:GSE46602
type
dataset
label
GEO GSE46602
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
pmid:38957390
type
paper
label
pmid:38957390
[1] object · 3 fields
id
source:pmid:38957390
type
manuscript
label
PMID 38957390 full text
[2] object · 3 fields
id
data:geo:GSE46602
type
dataset
label
GEO GSE46602
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-38957390
type
extraction
used array · 1 item
[0]
source:pmid:38957390
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE46602
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE46602
agent
agent:corpus-assay-engine
agents array · 2 items
[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:38957390
parent_hash
sha256:41147174d4cab57213b516ba2767ba1e2a7ab58cf8d328bbb541518963a6a599
fork_of
null
gaps array · 9 items
[0]
asset:data:geo:GSE46602 licence not read
[1]
asset:data:geo:GSE46602 not downloaded
[2]
asset:data:geo:GSE70770 licence not read
[3]
asset:data:geo:GSE70770 not downloaded
[4]
execution.not_run
[5]
method.reader_differs_from_extractor
[6]
review.human_critique
[7]
review.independent_reader
[8]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
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f2132e96ae6c7a4e
required_operations array · 1 item
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cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38957390", "kind": "science-record", "revision": 3, "content_hash": "sha256:aaccfff6508b1bdabf9e82a6442e575b74381977484618a98dc896621290ba59", "created_at": "2026-11-01T20:29:01Z", "updated_at": "2026-11-01T22:12:10Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of anoikis-related gene signatures and construction of the prognosis model in prostate cancer.", "doi": "10.3389/fphar.2024.1383304", "pmid": "38957390", "authors": ["Wanying Kang", "Chen Ye", "Yunyun Yang", "Yan-Ru Lou", "Mingyi Zhao", "Zhuo Wang", "Yuan Gao"], "journal": "Frontiers in pharmacology", "year": 2024, "abstract": "Background: One of the primary reasons for tumor invasion and metastasis is anoikis resistance. Biochemical recurrence (BCR) of prostate cancer (PCa) serves as a harbinger of its distant metastasis. However, the role of anoikis in PCa biochemical recurrence has not been fully elucidated.\nMethods: Differential expression analysis was used to identify anoikis-related genes based on the TCGA and GeneCards databases. Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses. Moreover, Gene Expression Omnibus datasets (GSE70770 and GSE46602) were applied as validation cohorts. Gene Ontology, KEGG and GSVA were utilized to explore biological pathways and molecular mechanisms. Further, immune profiles were assessed using CIBERSORT, ssGSEA, and TIDE, while anti-cancer drugs sensitivity was analyzed by GDSC database. In addition, gene expressions in the model were examined using online databases (Human Protein Atlas and Tumor Immune Single-Cell Hub).\nResults: 113 differentially expressed anoikis-related genes were found. Four genes (EEF1A2, RET, FOSL1, PCA3) were selected for constructing a prognostic model. Using the findings from the Cox regression analysis, we grouped patients into groups of high and low risk. The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897. Moreover, larger percentage of immune infiltration of memory B cells, CD8 Tcells, neutrophils, and M1 macrophages were observed in the high-risk group than those in the low-risk group, whereas the percentage of activated mast cells and dendritic cells in the high-risk group were lower. An increased TIDE score was founded in the high-risk group, suggesting reduced effectiveness of ICI therapy. Additionally, the IC50 results for chemotherapy drugs indicated that the low-risk group was more sensitive to most of the drugs. Finally, the genes EEF1A2, RET, and FOSL1 were expressed in PCa cases based on HPA website. The TISCH database suggested that these four ARGs might contribute to the tumor microenvironment of PCa.\nConclusion: We created a risk model utilizing four ARGs that effectively predicts the risk of BCR in PCa patients. This study lays the groundwork for risk stratification and predicting survival outcomes in PCa patients with BCR.", "claims": [{"id": "claim-method", "statement": "Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38957390", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Prognostic models were constructed utilizing LASSO regression, univariate and multivariate Cox regression analyses."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38957390", "locator": "sections[25] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.", "kind": "quantitative", "target": {"value": 0.897, "unit": "auc", "tolerance": null, "source": "The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897."}, "evidence": [{"asset": "source:pmid:38957390", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The high-risk group exhibited a poorer prognosis, with a maximum AUC of 0.897.", "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:38957390"], "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:GSE46602"], "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:GSE46602"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38957390", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fphar.2024.1383304", "sha256": 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