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pmid:41050938

Integrated analysis of stem cell-related genes shared between type 2 diabetes mellitus and sepsis.

Yubo Wang · Xinhai Jiang · Xiaohan Song · Zhijie Ma · Yan Wang

Frontiers in chemistry · 2025 doi:10.3389/fchem.2025.1666651

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:41050938
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science-record
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2026-11-01T20:31:06Z
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2026-11-01T22:57:15Z
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paper object · 10 fields
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title
Integrated analysis of stem cell-related genes shared between type 2 diabetes mellitus and sepsis.
doi
10.3389/fchem.2025.1666651
pmid
41050938
authors array · 5 items
[0]
Yubo Wang
[1]
Xinhai Jiang
[2]
Xiaohan Song
[3]
Zhijie Ma
[4]
Yan Wang
journal
Frontiers in chemistry
year
2025
abstract
Background: Diabetes-induced immune impairment and insulin resistance increase infection risk, which may progress to sepsis that further deteriorates diabetic status. Stem cell-based interventions show therapeutic potential for both diseases. This study sought to uncover common stem cell-related genes (SCRGs) between T2DM and sepsis. Methods: The GSE15932 dataset for T2DM and GSE65682 dataset for sepsis from the Gene Expression Omnibus (GEO) were utilized to locate common differentially expressed genes (DEGs), which were then intersected with SCRGs to derive shared differentially expressed SCRGs (DE-SCRGs). The stem-cell-related biomarkers were discovered through combining functional similarity analysis, machine learning algorithms, and receiver operating characteristic (ROC) curves. Subsequently, functional enrichment analysis, immune infiltration, and single-cell analyses were conducted to investigate the potential pathways by which biomarkers regulate T2DM and sepsis. Finally, the expression of biomarkers was further verified at both transcriptional and protein levels through the establishment of an in vitro model of T2DM-sepsis. Results: Through a comprehensive analysis, CAPG and DDAH2 were found and those were significantly highly expressed in both T2DM and sepsis. Analysis of functional enrichment demonstrated they were implicated in "FC gamma R-mediated phagocytosis" and "Ribosome". Immune infiltration indicated a considerable disparity in the quantity of CD8 T cells and monocytes when comparing T2DM versus control groups, as well as sepsis versus control groups. At the cellular level, notable differences in CARG expression among alpha cells, beta cells, delta cells, and pancreatic stellate cells (PSCs) were observed in the two groups being compared. At transcription and protein levels, CAPG and DDAH2 were significantly more highly expressed in the T2DM-sepsis model than in the controls. The results corroborated the bioinformatics analysis conclusions, reinforcing the study's validity. Conclusion: Two common stem cell-related biomarkers (CAPG and DDAH2) and their common pathways between T2DM and sepsis were discovered, providing new insights for further molecular mechanism studies.
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The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015).
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sections[4] "Differential expression analysis" paragraph 2
quote
The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015).
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The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
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sections[31] "Data availability statement" paragraph 2
quote
The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
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The study identified two shared stem cell-related biomarkers, CAPG and DDAH2, for T2DM and sepsis.
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sections[0] "Abstract" paragraph 4
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Two common stem cell-related biomarkers (CAPG and DDAH2) and their common pathways between T2DM and sepsis were discovered, providing new insights for further molecular mechanism studies.
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The study identified two shared stem cell-related biomarkers, CAPG and DDAH2, for T2DM and sepsis.
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The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
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[284]
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[285]
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[286]
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[287]
GSM1691975
[288]
GSM1691976
[289]
GSM1691977
[290]
GSM1691978
[291]
GSM1691979
[292]
GSM1691980
[293]
GSM1691981
[294]
GSM1691982
[295]
GSM1691983
[296]
GSM1691984
[297]
GSM1691985
[298]
GSM1691986
[299]
GSM1691987
[300]
GSM1691988
[301]
GSM1691989
[302]
GSM1691990
[303]
GSM1691991
[304]
GSM1691992
[305]
GSM1691993
[306]
GSM1691994
[307]
GSM1691995
[308]
GSM1691996
[309]
GSM1691997
[310]
GSM1691998
[311]
GSM1691999
[312]
GSM1692000
[313]
GSM1692001
[314]
GSM1692002
[315]
GSM1692003
[316]
GSM1692004
[317]
GSM1692005
[318]
GSM1692006
[319]
GSM1692007
[320]
GSM1692008
[321]
GSM1692009
[322]
GSM1692010
[323]
GSM1692011
[324]
GSM1692012
[325]
GSM1692015
[326]
GSM1692016
[327]
GSM1692017
[328]
GSM1692018
[329]
GSM1692019
[330]
GSM1692020
[331]
GSM1692021
[332]
GSM1692022
[333]
GSM1692023
[334]
GSM1692024
[335]
GSM1692025
[336]
GSM1692026
[337]
GSM1692027
[338]
GSM1692028
[339]
GSM1692029
[340]
GSM1692030
[341]
GSM1692032
[342]
GSM1692033
[343]
GSM1692034
[344]
GSM1692035
[345]
GSM1692036
[346]
GSM1692037
[347]
GSM1692038
[348]
GSM1692039
[349]
GSM1692040
[350]
GSM1692041
[351]
GSM1692042
[352]
GSM1692043
[353]
GSM1692044
[354]
GSM1692045
[355]
GSM1692046
[356]
GSM1692047
[357]
GSM1692048
[358]
GSM1692049
[359]
GSM1692050
[360]
GSM1692051
[361]
GSM1692052
[362]
GSM1692053
[363]
GSM1692054
[364]
GSM1692055
[365]
GSM1692056
[366]
GSM1692057
[367]
GSM1692058
[368]
GSM1692059
[369]
GSM1692060
[370]
GSM1692061
[371]
GSM1692062
[372]
GSM1692063
[373]
GSM1692064
[374]
GSM1692065
[375]
GSM1692066
[376]
GSM1692067
[377]
GSM1692068
[378]
GSM1692069
[379]
GSM1692070
[380]
GSM1692071
[381]
GSM1692072
[382]
GSM1692073
[383]
GSM1692074
[384]
GSM1692075
[385]
GSM1692077
[386]
GSM1692078
[387]
GSM1692079
[388]
GSM1692080
[389]
GSM1692081
[390]
GSM1692082
[391]
GSM1692083
[392]
GSM1692084
[393]
GSM1692085
[394]
GSM1692086
[395]
GSM1692087
[396]
GSM1692088
[397]
GSM1692089
[398]
GSM1692090
[399]
GSM1692091
[400]
GSM1692092
[401]
GSM1692093
[402]
GSM1692094
[403]
GSM1692095
[404]
GSM1692096
[405]
GSM1692097
[406]
GSM1692098
[407]
GSM1692099
[408]
GSM1692100
[409]
GSM1692101
[410]
GSM1692102
[411]
GSM1692103
[412]
GSM1692104
[413]
GSM1692105
[414]
GSM1692106
[415]
GSM1692107
[416]
GSM1692108
[417]
GSM1692109
[418]
GSM1692110
[419]
GSM1692111
[420]
GSM1692112
[421]
GSM1692114
[422]
GSM1692115
[423]
GSM1692116
[424]
GSM1692117
[425]
GSM1692118
[426]
GSM1692119
[427]
GSM1692120
[428]
GSM1692121
[429]
GSM1692122
[430]
GSM1692123
[431]
GSM1692124
[432]
GSM1692125
[433]
GSM1692126
[434]
GSM1692127
[435]
GSM1692128
[436]
GSM1692129
[437]
GSM1692130
[438]
GSM1692131
[439]
GSM1692132
[440]
GSM1692133
[441]
GSM1692135
[442]
GSM1692136
[443]
GSM1692137
[444]
GSM1692138
[445]
GSM1692139
[446]
GSM1692140
[447]
GSM1692141
[448]
GSM1692142
[449]
GSM1692143
[450]
GSM1692144
[451]
GSM1692145
[452]
GSM1692146
[453]
GSM1692147
[454]
GSM1692148
[455]
GSM1692149
[456]
GSM1692150
[457]
GSM1692151
[458]
GSM1692152
[459]
GSM1692153
[460]
GSM1692154
[461]
GSM1692155
[462]
GSM1692156
[463]
GSM1692157
[464]
GSM1692158
[465]
GSM1692159
[466]
GSM1692160
[467]
GSM1692161
[468]
GSM1692162
[469]
GSM1692163
[470]
GSM1692164
[471]
GSM1692165
[472]
GSM1692166
[473]
GSM1692167
[474]
GSM1692168
[475]
GSM1692169
[476]
GSM1692170
[477]
GSM1692171
[478]
GSM1692172
[479]
GSM1692173
[480]
GSM1692174
[481]
GSM1692175
[482]
GSM1692176
[483]
GSM1692177
[484]
GSM1692178
[485]
GSM1692179
[486]
GSM1692180
[487]
GSM1692181
[488]
GSM1692182
[489]
GSM1692183
[490]
GSM1692184
[491]
GSM1692185
[492]
GSM1692186
[493]
GSM1692187
[494]
GSM1692188
[495]
GSM1692189
[496]
GSM1692190
[497]
GSM1692191
[498]
GSM1692192
[499]
GSM1692193
[500]
GSM1692194
[501]
GSM1692195
[502]
GSM1692196
[503]
GSM1692197
[504]
GSM1692198
[505]
GSM1692199
[506]
GSM1692200
[507]
GSM1692201
[508]
GSM1692202
[509]
GSM1692203
[510]
GSM1692204
[511]
GSM1692205
[512]
GSM1692206
[513]
GSM1692207
[514]
GSM1692208
[515]
GSM1692209
[516]
GSM1692210
[517]
GSM1692211
[518]
GSM1692212
[519]
GSM1692213
[520]
GSM1692214
[521]
GSM1692215
[522]
GSM1692216
[523]
GSM1692217
[524]
GSM1692218
[525]
GSM1692219
[526]
GSM1692220
[527]
GSM1692221
[528]
GSM1692222
[529]
GSM1692223
[530]
GSM1692224
[531]
GSM1692225
[532]
GSM1692226
[533]
GSM1692227
[534]
GSM1692228
[535]
GSM1692229
[536]
GSM1692230
[537]
GSM1692231
[538]
GSM1692232
[539]
GSM1692233
[540]
GSM1692234
[541]
GSM1692235
[542]
GSM1692237
[543]
GSM1692238
[544]
GSM1692239
[545]
GSM1692240
[546]
GSM1692241
[547]
GSM1692242
[548]
GSM1692243
[549]
GSM1692244
[550]
GSM1692245
[551]
GSM1692246
[552]
GSM1692247
[553]
GSM1692248
[554]
GSM1692249
[555]
GSM1692250
[556]
GSM1692251
[557]
GSM1692252
[558]
GSM1692253
[559]
GSM1692254
[560]
GSM1692255
[561]
GSM1692256
[562]
GSM1692257
[563]
GSM1692258
[564]
GSM1692259
[565]
GSM1692260
[566]
GSM1692261
[567]
GSM1692262
[568]
GSM1692263
[569]
GSM1692264
[570]
GSM1692265
[571]
GSM1692266
[572]
GSM1692267
[573]
GSM1692268
[574]
GSM1692269
[575]
GSM1692270
[576]
GSM1692271
[577]
GSM1692272
[578]
GSM1692273
[579]
GSM1692274
[580]
GSM1692275
[581]
GSM1692276
[582]
GSM1692277
[583]
GSM1692278
[584]
GSM1692279
[585]
GSM1692280
[586]
GSM1692281
[587]
GSM1692282
[588]
GSM1692283
[589]
GSM1692284
[590]
GSM1692286
[591]
GSM1692287
[592]
GSM1692288
[593]
GSM1692289
[594]
GSM1692290
[595]
GSM1692291
[596]
GSM1692292
[597]
GSM1692293
[598]
GSM1692294
[599]
GSM1692295
[600]
GSM1692296
[601]
GSM1692297
[602]
GSM1692298
[603]
GSM1692299
[604]
GSM1692300
[605]
GSM1692301
[606]
GSM1692302
[607]
GSM1692303
[608]
GSM1692304
[609]
GSM1692305
[610]
GSM1692306
[611]
GSM1692307
[612]
GSM1692308
[613]
GSM1692309
[614]
GSM1692310
[615]
GSM1692311
[616]
GSM1692312
[617]
GSM1692313
[618]
GSM1692314
[619]
GSM1692315
[620]
GSM1692316
[621]
GSM1692317
[622]
GSM1692318
[623]
GSM1692319
[624]
GSM1692320
[625]
GSM1692321
[626]
GSM1692322
[627]
GSM1692323
[628]
GSM1692324
[629]
GSM1692326
[630]
GSM1692327
[631]
GSM1692328
[632]
GSM1692329
[633]
GSM1692330
[634]
GSM1692331
[635]
GSM1692332
[636]
GSM1692333
[637]
GSM1692334
[638]
GSM1692335
[639]
GSM1692336
[640]
GSM1692337
[641]
GSM1692338
[642]
GSM1692339
[643]
GSM1692340
[644]
GSM1692341
[645]
GSM1692342
[646]
GSM1692343
[647]
GSM1692344
[648]
GSM1692345
[649]
GSM1692346
[650]
GSM1692347
[651]
GSM1692348
[652]
GSM1692349
[653]
GSM1692350
[654]
GSM1692352
[655]
GSM1692353
[656]
GSM1692354
[657]
GSM1692355
[658]
GSM1692356
[659]
GSM1692357
[660]
GSM1692358
[661]
GSM1692359
[662]
GSM1692360
[663]
GSM1692361
[664]
GSM1692362
[665]
GSM1692363
[666]
GSM1692364
[667]
GSM1692365
[668]
GSM1692366
[669]
GSM1692367
[670]
GSM1692368
[671]
GSM1692369
[672]
GSM1692370
[673]
GSM1692371
[674]
GSM1692372
[675]
GSM1692373
[676]
GSM1692374
[677]
GSM1692375
[678]
GSM1692376
[679]
GSM1692377
[680]
GSM1692378
[681]
GSM1692379
[682]
GSM1692380
[683]
GSM1692381
[684]
GSM1692382
[685]
GSM1692383
[686]
GSM1692384
[687]
GSM1692385
[688]
GSM1692386
[689]
GSM1692387
[690]
GSM1692388
[691]
GSM1692389
[692]
GSM1692390
[693]
GSM1692391
[694]
GSM1692392
[695]
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[696]
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[697]
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[698]
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[699]
GSM1692397
[700]
GSM1692398
[701]
GSM1692399
[702]
GSM1692400
[703]
GSM1692402
[704]
GSM1692404
[705]
GSM1692405
[706]
GSM1692406
[707]
GSM1692407
[708]
GSM1692408
[709]
GSM1692409
[710]
GSM1692410
[711]
GSM1692411
[712]
GSM1692412
[713]
GSM1692413
[714]
GSM1692414
[715]
GSM1692415
[716]
GSM1692416
[717]
GSM1692417
[718]
GSM1692418
[719]
GSM1692419
[720]
GSM1692420
[721]
GSM1692421
[722]
GSM1692422
[723]
GSM1692423
[724]
GSM1692424
[725]
GSM1692425
[726]
GSM1692426
[727]
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[728]
GSM1692428
[729]
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[730]
GSM1692430
[731]
GSM1692431
[732]
GSM1692432
[733]
GSM1692433
[734]
GSM1692434
[735]
GSM1692435
[736]
GSM1692436
[737]
GSM1692437
[738]
GSM1692438
[739]
GSM1692439
[740]
GSM1692440
[741]
GSM1692441
[742]
GSM1692442
[743]
GSM1692443
[744]
GSM1692444
[745]
GSM1692445
[746]
GSM1692446
[747]
GSM1692447
[748]
GSM1692448
[749]
GSM1692449
[750]
GSM1692450
[751]
GSM1692451
[752]
GSM1692452
[753]
GSM1692453
[754]
GSM1692454
[755]
GSM1692455
[756]
GSM1692456
[757]
GSM1692457
[758]
GSM1692458
[759]
GSM1692459
[760]
GSM1692460
[761]
GSM1692461
[762]
GSM1692462
[763]
GSM1692463
[764]
GSM1692465
[765]
GSM1692466
[766]
GSM1692467
[767]
GSM1692468
[768]
GSM1692469
[769]
GSM1692470
[770]
GSM1692471
[771]
GSM1692472
[772]
GSM1692473
[773]
GSM1692474
[774]
GSM1692475
[775]
GSM1692476
[776]
GSM1692477
[777]
GSM1692478
[778]
GSM1692479
[779]
GSM1692480
[780]
GSM1692481
[781]
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[782]
GSM1692483
[783]
GSM1692484
[784]
GSM1692485
[785]
GSM1692487
[786]
GSM1692488
[787]
GSM1692489
[788]
GSM1692490
[789]
GSM1692491
[790]
GSM1692492
[791]
GSM1692493
[792]
GSM1692494
[793]
GSM1692495
[794]
GSM1692496
[795]
GSM1692497
[796]
GSM1692498
[797]
GSM1692499
[798]
GSM1692501
[799]
GSM1692502
[800]
GSM1692503
[801]
GSM1692504
sample_count
802
group_sizes
null
group_sizes_basis
null
platform
13667
taxon
Homo sapiens
title
Genome-wide blood transcriptional profiling in critically ill patients - MARS consortium
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[5] object · 15 fields
id
data:geo:GSE95233
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=GSE95233
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE95233
version
null
note
The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
access_statement_kind
data_availability_statement
sample_accessions array · 124 items
[0]
GSM2500349
[1]
GSM2500350
[2]
GSM2500351
[3]
GSM2500352
[4]
GSM2500353
[5]
GSM2500354
[6]
GSM2500355
[7]
GSM2500356
[8]
GSM2500357
[9]
GSM2500358
[10]
GSM2500359
[11]
GSM2500360
[12]
GSM2500361
[13]
GSM2500362
[14]
GSM2500363
[15]
GSM2500364
[16]
GSM2500365
[17]
GSM2500366
[18]
GSM2500367
[19]
GSM2500368
[20]
GSM2500369
[21]
GSM2500370
[22]
GSM2500371
[23]
GSM2500372
[24]
GSM2500373
[25]
GSM2500374
[26]
GSM2500375
[27]
GSM2500376
[28]
GSM2500377
[29]
GSM2500378
[30]
GSM2500379
[31]
GSM2500380
[32]
GSM2500381
[33]
GSM2500382
[34]
GSM2500383
[35]
GSM2500384
[36]
GSM2500385
[37]
GSM2500386
[38]
GSM2500387
[39]
GSM2500388
[40]
GSM2500389
[41]
GSM2500390
[42]
GSM2500391
[43]
GSM2500392
[44]
GSM2500393
[45]
GSM2500394
[46]
GSM2500395
[47]
GSM2500396
[48]
GSM2500397
[49]
GSM2500398
[50]
GSM2500399
[51]
GSM2500400
[52]
GSM2500401
[53]
GSM2500402
[54]
GSM2500403
[55]
GSM2500404
[56]
GSM2500405
[57]
GSM2500406
[58]
GSM2500407
[59]
GSM2500408
[60]
GSM2500409
[61]
GSM2500410
[62]
GSM2500411
[63]
GSM2500412
[64]
GSM2500413
[65]
GSM2500414
[66]
GSM2500415
[67]
GSM2500416
[68]
GSM2500417
[69]
GSM2500418
[70]
GSM2500419
[71]
GSM2500420
[72]
GSM2500421
[73]
GSM2500422
[74]
GSM2500423
[75]
GSM2500424
[76]
GSM2500425
[77]
GSM2500426
[78]
GSM2500427
[79]
GSM2500428
[80]
GSM2500429
[81]
GSM2500430
[82]
GSM2500431
[83]
GSM2500432
[84]
GSM2500433
[85]
GSM2500434
[86]
GSM2500435
[87]
GSM2500436
[88]
GSM2500437
[89]
GSM2500438
[90]
GSM2500439
[91]
GSM2500440
[92]
GSM2500441
[93]
GSM2500442
[94]
GSM2500443
[95]
GSM2500444
[96]
GSM2500445
[97]
GSM2500446
[98]
GSM2500447
[99]
GSM2500448
[100]
GSM2500449
[101]
GSM2500450
[102]
GSM2500451
[103]
GSM2500452
[104]
GSM2500453
[105]
GSM2500454
[106]
GSM2500455
[107]
GSM2500456
[108]
GSM2500457
[109]
GSM2500458
[110]
GSM2500459
[111]
GSM2500460
[112]
GSM2500461
[113]
GSM2500462
[114]
GSM2500463
[115]
GSM2500464
[116]
GSM2500465
[117]
GSM2500466
[118]
GSM2500467
[119]
GSM2500468
[120]
GSM2500469
[121]
GSM2500470
[122]
GSM2500471
[123]
GSM2500472
sample_count
124
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Fractalkine receptor CX3CR1 and leukocyte Ig-like receptor B2 LILRB2 are prognostic biomarkers in septic shock
resolution_checked_at
2026-11-01T15:39:55Z
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identifier_resolution_only_no_download_no_licence_read
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[3]
asset:data:geo:GSE195986 licence not read
[4]
asset:data:geo:GSE20966 not downloaded
[5]
asset:data:geo:GSE20966 licence not read
[6]
asset:data:geo:GSE65682 not downloaded
[7]
asset:data:geo:GSE65682 licence not read
[8]
asset:data:geo:GSE95233 not downloaded
[9]
asset:data:geo:GSE95233 licence not read
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state
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method-1
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normalise_counts
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differential_expression_fit
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count_matrix_with_condition
evidence object · 3 fields
score
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quote
The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015).
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group_comparison
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wilcoxon
label
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missing_operations array · 1 item
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group_comparison_wilcoxon
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false
parameters object · 1 field
sample_size
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two_or_more_groups_continuous
evidence object · 3 fields
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0.8
band
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quote
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gaps array · 1 item
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method.reader_differs_from_extractor
capability object · 3 fields
state
complete
requirements array · 1 item
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capability:computational_analysis
label
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assay_families array · 9 items
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meta_analysis
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machine_learning
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molecular_docking
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network_analysis
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differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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method object · 5 fields
tier
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normalise_counts
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differential_expression_fit
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fdr_bh
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
capability object · 4 fields
tier
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capability:computational_analysis
availability_state
owned
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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
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accessions array · 5 items
[0]
GSE15932
[1]
GSE20966
[2]
GSE65682
[3]
GSE95233
[4]
GSE195986
resolved_accessions array · 5 items
[0]
GSE15932
[1]
GSE20966
[2]
GSE65682
[3]
GSE95233
[4]
GSE195986
statements array · 1 item
[0]
The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).
basis
The paper names GSE15932, GSE20966, GSE65682, GSE95233, GSE195986 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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[1]
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data:geo:GSE15932
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run_analysis
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readers array · 0 items
capabilities array · 0 items
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data:geo:GSE15932
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
2026-11-01T20:02:25Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
usage object · 3 fields
prompt_tokens
13251
completion_tokens
1545
cached_tokens
264
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id
extraction
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complete
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MiniMax-M3.1-Flash
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entities array · 3 items
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pmid:41050938
type
paper
label
pmid:41050938
[1] object · 3 fields
id
source:pmid:41050938
type
manuscript
label
PMID 41050938 full text
[2] object · 3 fields
id
data:geo:GSE15932
type
dataset
label
GEO GSE15932
activities array · 3 items
[0] object · 4 fields
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activity-reading-sci-2026-11-01
type
classification
used array · 3 items
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pmid:41050938
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paper
label
pmid:41050938
[1] object · 3 fields
id
source:pmid:41050938
type
manuscript
label
PMID 41050938 full text
[2] object · 3 fields
id
data:geo:GSE15932
type
dataset
label
GEO GSE15932
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-41050938
type
extraction
used array · 1 item
[0]
source:pmid:41050938
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE15932
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE15932
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
type
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label
MiniMax literature reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
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lineage object · 4 fields
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[3]
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[4]
asset:data:geo:GSE20966 licence not read
[5]
asset:data:geo:GSE20966 not downloaded
[6]
asset:data:geo:GSE65682 licence not read
[7]
asset:data:geo:GSE65682 not downloaded
[8]
asset:data:geo:GSE95233 licence not read
[9]
asset:data:geo:GSE95233 not downloaded
[10]
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[12]
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assays array · 3 items
[0] object · 11 fields
role
data_generation
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scrna_seq
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[0]
s (Figure 7D). DDAH2 was not detected in the scRNA-seq dataset due to the absence of information fo
[1]
(Supplementary Table S7). As no blood-based scRNA-seq datasets with case–control design were avail
order_basis
paper_text_order:4992
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[0]
(E) The volcano plot showing the DEGs of the RNA-seq dataset (F) The expression of each biomarker
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evidence array · 1 item
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The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41050938", "kind": "science-record", "revision": 4, "content_hash": "sha256:8441734e39aad38ee7a2fbac81845116f247c020b1759484cd945d90eb1ae228", "created_at": "2026-11-01T20:31:06Z", "updated_at": "2026-11-01T22:57:15Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated analysis of stem cell-related genes shared between type 2 diabetes mellitus and sepsis.", "doi": "10.3389/fchem.2025.1666651", "pmid": "41050938", "authors": ["Yubo Wang", "Xinhai Jiang", "Xiaohan Song", "Zhijie Ma", "Yan Wang"], "journal": "Frontiers in chemistry", "year": 2025, "abstract": "Background: Diabetes-induced immune impairment and insulin resistance increase infection risk, which may progress to sepsis that further deteriorates diabetic status. Stem cell-based interventions show therapeutic potential for both diseases. This study sought to uncover common stem cell-related genes (SCRGs) between T2DM and sepsis.\nMethods: The GSE15932 dataset for T2DM and GSE65682 dataset for sepsis from the Gene Expression Omnibus (GEO) were utilized to locate common differentially expressed genes (DEGs), which were then intersected with SCRGs to derive shared differentially expressed SCRGs (DE-SCRGs). The stem-cell-related biomarkers were discovered through combining functional similarity analysis, machine learning algorithms, and receiver operating characteristic (ROC) curves. Subsequently, functional enrichment analysis, immune infiltration, and single-cell analyses were conducted to investigate the potential pathways by which biomarkers regulate T2DM and sepsis. Finally, the expression of biomarkers was further verified at both transcriptional and protein levels through the establishment of an in vitro model of T2DM-sepsis.\nResults: Through a comprehensive analysis, CAPG and DDAH2 were found and those were significantly highly expressed in both T2DM and sepsis. Analysis of functional enrichment demonstrated they were implicated in \"FC gamma R-mediated phagocytosis\" and \"Ribosome\". Immune infiltration indicated a considerable disparity in the quantity of CD8 T cells and monocytes when comparing T2DM versus control groups, as well as sepsis versus control groups. At the cellular level, notable differences in CARG expression among alpha cells, beta cells, delta cells, and pancreatic stellate cells (PSCs) were observed in the two groups being compared. At transcription and protein levels, CAPG and DDAH2 were significantly more highly expressed in the T2DM-sepsis model than in the controls. The results corroborated the bioinformatics analysis conclusions, reinforcing the study's validity.\nConclusion: Two common stem cell-related biomarkers (CAPG and DDAH2) and their common pathways between T2DM and sepsis were discovered, providing new insights for further molecular mechanism studies.", "claims": [{"id": "claim-method", "statement": "The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41050938", "locator": "sections[4] \"Differential expression analysis\" paragraph 2", "quote": "The “limma” R package (version 3.54.2) was utilized to investigate differentially expressed genes (DEGs) between T2DM and control groups in GSE15932 with |log fold change| (|logFC|) > 0.5 and P-value <0.05 as screening thresholds (Ritchie et al., 2015)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41050938", "locator": "sections[31] \"Data availability statement\" paragraph 2", "quote": "The datasets (GSE15932, GSE20966, GSE65682, GSE95233, and GSE195986) analyzed in this study were collected from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified two shared stem cell-related biomarkers, CAPG and DDAH2, for T2DM and sepsis.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:41050938", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Two common stem cell-related biomarkers (CAPG and DDAH2) and their common pathways between T2DM and sepsis were discovered, providing new insights for further molecular mechanism studies."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified two shared stem cell-related biomarkers, CAPG and DDAH2, for T2DM and sepsis.", "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:41050938"], "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:GSE15932"], "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:GSE15932"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:41050938", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fchem.2025.1666651", "sha256": 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