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pmid:39872516

Construction of an anaplastic thyroid cancer stratification signature to guide immune therapy selection and validation of the pivotal gene HLF through in vitro experiments.

Li Pengping · Yin Kexin · Xie Yuwei · Sun Ke · Li Rongguo · Wang Zhenyu · Jin Haigang · Wang Shaowen · Huang Yuqing

Frontiers in immunology · 2024 doi:10.3389/fimmu.2024.1478904

Paper

complete

Experiment

partial

Data

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Analysis

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title
Construction of an anaplastic thyroid cancer stratification signature to guide immune therapy selection and validation of the pivotal gene HLF through in vitro experiments.
doi
10.3389/fimmu.2024.1478904
pmid
39872516
authors array · 9 items
[0]
Li Pengping
[1]
Yin Kexin
[2]
Xie Yuwei
[3]
Sun Ke
[4]
Li Rongguo
[5]
Wang Zhenyu
[6]
Jin Haigang
[7]
Wang Shaowen
[8]
Huang Yuqing
journal
Frontiers in immunology
year
2024
abstract
Introduction: While most thyroid cancer patients have a favorable prognosis, anaplastic thyroid carcinoma (ATC) remains a particularly aggressive form with a median survival time of just five months. Conventional therapies offer limited benefits for this type of thyroid cancer. Our study aims to identify ATC patients who might bene t from immunotherapy. Methods: Our study uses multiple algorithms by R4.2.0, and gene expression and clinical data are collected from TCGA, GEO and local cohort. In vitro experiments, such as western blot and immunofluorescence staining, are performed. Results: Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients (GSE60542, GSE76039, GSE33630, GSE53157, GSE65144, GSE29265, GSE82208, GSE27155, GSE58545, GSE54958, and GSE32662). These genes allowed us to stratify ATC into three distinct groups, each exhibiting significantly different responses to anti-PD1 therapy as determined by consensus clustering. Through weighted gene co-expression network analysis (WGCNA), we identified 12 differentially expressed genes closely associated with immunotherapy outcomes. This led to the creation of a refined signature for predicting ATC's immune responsiveness to anti-PD1 therapy, which was further validated using thyroid cancer cohorts from TCGA and nine melanoma cohorts from clinical trials. Among the 12 genes, HLF stood out due to its strong association with various cancer hallmarks. Discussion: Our study revealed that HLF impedes ATC progression by down-regulating the epithelial-to-mesenchymal transition (EMT) pathway, reducing T cell exhaustion, and increasing sensitivity to sorafenib, as demonstrated through our in-vitro experiments.
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Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0).
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sections[10] "The 12-gene signature construction" paragraph 2
quote
Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0).
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Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients.
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Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients (GSE60542, GSE76039, GSE33630, GSE53157, GSE65144, GSE29265, GSE82208, GSE27155, GSE58545, GSE54958, and GSE32662).
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Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients.
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GSM1283131
[17]
GSM1283132
[18]
GSM1283133
[19]
GSM1283134
[20]
GSM1283135
[21]
GSM1283136
[22]
GSM1283137
[23]
GSM1283138
[24]
GSM1283139
[25]
GSM1283140
[26]
GSM1283141
sample_count
27
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression profiling associated with the progression to poorly differentiated thyroid carcinomas
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[6] object · 15 fields
id
data:geo:GSE54958
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=GSE54958
sha256
null
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null
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null
reader_status
reader_required
identifier
GSE54958
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 45 items
[0]
GSM1327231
[1]
GSM1327232
[2]
GSM1327233
[3]
GSM1327234
[4]
GSM1327235
[5]
GSM1327236
[6]
GSM1327237
[7]
GSM1327238
[8]
GSM1327239
[9]
GSM1327240
[10]
GSM1327241
[11]
GSM1327242
[12]
GSM1327243
[13]
GSM1327244
[14]
GSM1327245
[15]
GSM1327246
[16]
GSM1327247
[17]
GSM1327248
[18]
GSM1327249
[19]
GSM1327250
[20]
GSM1327251
[21]
GSM1327252
[22]
GSM1327253
[23]
GSM1327254
[24]
GSM1327255
[25]
GSM1327256
[26]
GSM1327257
[27]
GSM1327258
[28]
GSM1327259
[29]
GSM1327260
[30]
GSM1327261
[31]
GSM1327262
[32]
GSM1327263
[33]
GSM1327264
[34]
GSM1327265
[35]
GSM1327266
[36]
GSM1327267
[37]
GSM1327268
[38]
GSM1327269
[39]
GSM1327270
[40]
GSM1327271
[41]
GSM1327272
[42]
GSM1327273
[43]
GSM1327274
[44]
GSM1327275
sample_count
45
group_sizes
null
group_sizes_basis
null
platform
6244
taxon
Homo sapiens
title
Expression profiling in proliferative thyroid lesions of different histologies and normal thyroid tissue
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[7] object · 15 fields
id
data:geo:GSE58545
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=GSE58545
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null
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reader_status
reader_required
identifier
GSE58545
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 45 items
[0]
GSM1413225
[1]
GSM1413226
[2]
GSM1413227
[3]
GSM1413228
[4]
GSM1413229
[5]
GSM1413230
[6]
GSM1413231
[7]
GSM1413232
[8]
GSM1413233
[9]
GSM1413234
[10]
GSM1413235
[11]
GSM1413236
[12]
GSM1413237
[13]
GSM1413238
[14]
GSM1413239
[15]
GSM1413240
[16]
GSM1413241
[17]
GSM1413242
[18]
GSM1413243
[19]
GSM1413244
[20]
GSM1413245
[21]
GSM1413246
[22]
GSM1413247
[23]
GSM1413248
[24]
GSM1413249
[25]
GSM1413250
[26]
GSM1413251
[27]
GSM1413252
[28]
GSM1413253
[29]
GSM1413254
[30]
GSM1413255
[31]
GSM1413256
[32]
GSM1413257
[33]
GSM1413258
[34]
GSM1413259
[35]
GSM1413260
[36]
GSM1413261
[37]
GSM1413262
[38]
GSM1413263
[39]
GSM1413264
[40]
GSM1413265
[41]
GSM1413266
[42]
GSM1413267
[43]
GSM1413268
[44]
GSM1413269
sample_count
45
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
Gene expression signature associated with BRAFV600E mutation in human papillary thyroid carcinoma based on transgenic mouse model (human)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[8] object · 15 fields
id
data:geo:GSE60542
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=GSE60542
sha256
null
bytes
null
access
open
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null
reader_status
reader_required
identifier
GSE60542
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 92 items
[0]
GSM1481838
[1]
GSM1481839
[2]
GSM1481840
[3]
GSM1481841
[4]
GSM1481842
[5]
GSM1481843
[6]
GSM1481844
[7]
GSM1481845
[8]
GSM1481846
[9]
GSM1481847
[10]
GSM1481848
[11]
GSM1481849
[12]
GSM1481850
[13]
GSM1481851
[14]
GSM1481852
[15]
GSM1481853
[16]
GSM1481854
[17]
GSM1481855
[18]
GSM1481856
[19]
GSM1481857
[20]
GSM1481858
[21]
GSM1481859
[22]
GSM1481860
[23]
GSM1481861
[24]
GSM1481862
[25]
GSM1481863
[26]
GSM1481864
[27]
GSM1481865
[28]
GSM1481866
[29]
GSM1481867
[30]
GSM1481868
[31]
GSM1481869
[32]
GSM1481870
[33]
GSM1481871
[34]
GSM1481872
[35]
GSM1481873
[36]
GSM1481874
[37]
GSM1481875
[38]
GSM1481876
[39]
GSM1481877
[40]
GSM1481878
[41]
GSM1481879
[42]
GSM1481880
[43]
GSM1481881
[44]
GSM1481882
[45]
GSM1481883
[46]
GSM1481884
[47]
GSM1481885
[48]
GSM1481886
[49]
GSM1481887
[50]
GSM1481888
[51]
GSM1481889
[52]
GSM1481890
[53]
GSM1481891
[54]
GSM1481892
[55]
GSM1481893
[56]
GSM1481894
[57]
GSM1481895
[58]
GSM1481896
[59]
GSM1481897
[60]
GSM1481898
[61]
GSM1481899
[62]
GSM1481900
[63]
GSM1481901
[64]
GSM1481902
[65]
GSM1481903
[66]
GSM1481904
[67]
GSM1481905
[68]
GSM1481906
[69]
GSM1481907
[70]
GSM1481908
[71]
GSM1481909
[72]
GSM1481910
[73]
GSM1481911
[74]
GSM1481912
[75]
GSM1481913
[76]
GSM1481914
[77]
GSM1481915
[78]
GSM1481916
[79]
GSM1481917
[80]
GSM1481918
[81]
GSM1481919
[82]
GSM1481920
[83]
GSM1481921
[84]
GSM1481922
[85]
GSM1481923
[86]
GSM1481924
[87]
GSM1481925
[88]
GSM1481926
[89]
GSM1481927
[90]
GSM1481928
[91]
GSM1481929
sample_count
92
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Revisiting the transcriptional analysis of primary tumors and associated nodal metastases with enhanced biological and statistical controls: application to thyroid cancer
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[9] object · 15 fields
id
data:geo:GSE65144
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=GSE65144
sha256
null
bytes
null
access
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null
reader_status
reader_required
identifier
GSE65144
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 25 items
[0]
GSM1588026
[1]
GSM1588027
[2]
GSM1588028
[3]
GSM1588029
[4]
GSM1588030
[5]
GSM1588031
[6]
GSM1588032
[7]
GSM1588033
[8]
GSM1588034
[9]
GSM1588035
[10]
GSM1588036
[11]
GSM1588037
[12]
GSM1588038
[13]
GSM1588039
[14]
GSM1588040
[15]
GSM1588041
[16]
GSM1588042
[17]
GSM1588043
[18]
GSM1588044
[19]
GSM1588045
[20]
GSM1588046
[21]
GSM1588047
[22]
GSM1588048
[23]
GSM1588049
[24]
GSM1588050
sample_count
25
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene array analysis of anaplastic thyroid carcinoma tissue versus matched and unmatched normal thyroid tissue
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[10] object · 15 fields
id
data:geo:GSE76039
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=GSE76039
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE76039
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 37 items
[0]
GSM2024824
[1]
GSM2024825
[2]
GSM2024826
[3]
GSM2024827
[4]
GSM2024828
[5]
GSM2024829
[6]
GSM2024830
[7]
GSM2024831
[8]
GSM2024832
[9]
GSM2024833
[10]
GSM2024834
[11]
GSM2024835
[12]
GSM2024836
[13]
GSM2024837
[14]
GSM2024838
[15]
GSM2024839
[16]
GSM2024840
[17]
GSM2024841
[18]
GSM2024842
[19]
GSM2024843
[20]
GSM2024844
[21]
GSM2024845
[22]
GSM2024846
[23]
GSM2024847
[24]
GSM2024848
[25]
GSM2024849
[26]
GSM2024850
[27]
GSM2024851
[28]
GSM2024852
[29]
GSM2024853
[30]
GSM2024854
[31]
GSM2024855
[32]
GSM2024856
[33]
GSM2024857
[34]
GSM2024858
[35]
GSM2024859
[36]
GSM2024860
sample_count
37
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Genomic and Transcriptomic Hallmarks of Poorly-Differentiated and Anaplastic Thyroid Cancers
resolution_checked_at
2026-11-01T17:30:42Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[11] object · 15 fields
id
data:geo:GSE82208
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=GSE82208
sha256
null
bytes
null
access
open
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resolved
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null
reader_status
reader_required
identifier
GSE82208
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 52 items
[0]
GSM2186533
[1]
GSM2186534
[2]
GSM2186535
[3]
GSM2186536
[4]
GSM2186537
[5]
GSM2186538
[6]
GSM2186539
[7]
GSM2186540
[8]
GSM2186541
[9]
GSM2186542
[10]
GSM2186543
[11]
GSM2186544
[12]
GSM2186545
[13]
GSM2186546
[14]
GSM2186547
[15]
GSM2186548
[16]
GSM2186549
[17]
GSM2186550
[18]
GSM2186551
[19]
GSM2186552
[20]
GSM2186553
[21]
GSM2186554
[22]
GSM2186555
[23]
GSM2186556
[24]
GSM2186557
[25]
GSM2186558
[26]
GSM2186559
[27]
GSM2186560
[28]
GSM2186561
[29]
GSM2186562
[30]
GSM2186563
[31]
GSM2186564
[32]
GSM2186565
[33]
GSM2186566
[34]
GSM2186567
[35]
GSM2186568
[36]
GSM2186569
[37]
GSM2186570
[38]
GSM2186571
[39]
GSM2186572
[40]
GSM2186573
[41]
GSM2186574
[42]
GSM2186575
[43]
GSM2186576
[44]
GSM2186577
[45]
GSM2186578
[46]
GSM2186579
[47]
GSM2186580
[48]
GSM2186581
[49]
GSM2186582
[50]
GSM2186583
[51]
GSM2186584
sample_count
52
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression markers differentiating between malignant and benign follicular thyroid tumors
resolution_checked_at
2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[12] object · 15 fields
id
data:geo:GSE91061
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=GSE91061
sha256
null
bytes
null
access
open
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null
reader_status
reader_required
identifier
GSE91061
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 109 items
[0]
GSM2420259
[1]
GSM2420260
[2]
GSM2420261
[3]
GSM2420262
[4]
GSM2420263
[5]
GSM2420264
[6]
GSM2420265
[7]
GSM2420266
[8]
GSM2420267
[9]
GSM2420268
[10]
GSM2420269
[11]
GSM2420270
[12]
GSM2420271
[13]
GSM2420272
[14]
GSM2420273
[15]
GSM2420274
[16]
GSM2420275
[17]
GSM2420276
[18]
GSM2420277
[19]
GSM2420278
[20]
GSM2420279
[21]
GSM2420280
[22]
GSM2420281
[23]
GSM2420282
[24]
GSM2420283
[25]
GSM2420284
[26]
GSM2420285
[27]
GSM2420286
[28]
GSM2420287
[29]
GSM2420288
[30]
GSM2420289
[31]
GSM2420290
[32]
GSM2420291
[33]
GSM2420292
[34]
GSM2420293
[35]
GSM2420294
[36]
GSM2420295
[37]
GSM2420296
[38]
GSM2420297
[39]
GSM2420298
[40]
GSM2420299
[41]
GSM2420300
[42]
GSM2420301
[43]
GSM2420302
[44]
GSM2420303
[45]
GSM2420304
[46]
GSM2420305
[47]
GSM2420306
[48]
GSM2420307
[49]
GSM2420308
[50]
GSM2420310
[51]
GSM2420311
[52]
GSM2420312
[53]
GSM2420313
[54]
GSM2420316
[55]
GSM2420317
[56]
GSM2420318
[57]
GSM2420319
[58]
GSM2420320
[59]
GSM2420323
[60]
GSM2420324
[61]
GSM2420325
[62]
GSM2420326
[63]
GSM2420328
[64]
GSM2420329
[65]
GSM2420331
[66]
GSM2420332
[67]
GSM2420333
[68]
GSM2420334
[69]
GSM2420335
[70]
GSM2420336
[71]
GSM2420337
[72]
GSM2420338
[73]
GSM2420339
[74]
GSM2420340
[75]
GSM2420341
[76]
GSM2420342
[77]
GSM2420343
[78]
GSM2420344
[79]
GSM2420345
[80]
GSM2420346
[81]
GSM2420349
[82]
GSM2420350
[83]
GSM2420351
[84]
GSM2420352
[85]
GSM2420353
[86]
GSM2420354
[87]
GSM2420355
[88]
GSM2420356
[89]
GSM2420357
[90]
GSM2420358
[91]
GSM2420359
[92]
GSM2420360
[93]
GSM2420361
[94]
GSM2420362
[95]
GSM2420363
[96]
GSM2420364
[97]
GSM2420365
[98]
GSM2420366
[99]
GSM2420367
[100]
GSM2420368
[101]
GSM2420369
[102]
GSM2420370
[103]
GSM2420371
[104]
GSM2420372
[105]
GSM2420373
[106]
GSM2420374
[107]
GSM2420375
[108]
GSM2420376
sample_count
109
group_sizes
null
group_sizes_basis
null
platform
9052
taxon
Homo sapiens
title
Molecular portraits of tumor mutational and micro-environmental sculpting by immune checkpoint blockade therapy
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[13] object · 15 fields
id
data:geo:PRJEB23709
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=PRJEB23709
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null
bytes
null
access
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reader_status
reader_required
identifier
PRJEB23709
version
null
note
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 0 items
sample_count
null
group_sizes
null
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null
platform
null
taxon
null
title
null
resolution_checked_at
2026-11-01T18:46:43Z
resolution_check
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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]
asset:data:geo:GSE33630 licence not read
[8]
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[9]
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[10]
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[11]
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[12]
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[13]
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[14]
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[15]
asset:data:geo:GSE60542 licence not read
[16]
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[17]
asset:data:geo:GSE65144 licence not read
[18]
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[19]
asset:data:geo:GSE76039 licence not read
[20]
asset:data:geo:GSE82208 not downloaded
[21]
asset:data:geo:GSE82208 licence not read
[22]
asset:data:geo:GSE91061 not downloaded
[23]
asset:data:geo:GSE91061 licence not read
[24]
asset:data:geo:PRJEB23709 not downloaded
[25]
asset:data:geo:PRJEB23709 licence not read
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quote
Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0).
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formed to calculate the hazard ratio (HR), and the log-rank
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Cox regression
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formed to calculate the hazard ratio (HR), and the log-rank
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0.8
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capability:computational_analysis
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statistical_regression
[4]
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[6]
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candidate
Automated Assays Laravel application and simulated adapters
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: random_forest.
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tier
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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
tier
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[0]
GSE27155
[1]
GSE58545
[2]
GSE76039
[3]
GSE82208
[4]
GSE60542
[5]
GSE29265
[6]
GSE33630
[7]
GSE65144
[8]
GSE53157
[9]
GSE54958
[10]
and GSE32662
[11]
GSE115821 (N=37)
[12]
GSE78220 (N=28)
[13]
GSE91061 (N=109)
[14]
and PRJEB23709 (N=91)
[15]
GSE115821
[16]
GSE91061
[17]
PRJEB23709
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[0]
GSE27155
[1]
GSE58545
[2]
GSE76039
[3]
GSE82208
[4]
GSE60542
[5]
GSE29265
[6]
GSE33630
[7]
GSE65144
[8]
GSE53157
[9]
GSE54958
[10]
GSE115821
[11]
GSE91061
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
basis
The paper names GSE27155, GSE58545, GSE76039, GSE82208, GSE60542, GSE29265, GSE33630, GSE65144, GSE53157, GSE54958, GSE115821, GSE91061 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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machine_learning_random_forest
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reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T19:45:20Z
independence
single_reader
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paper
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pmid:39872516
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source:pmid:39872516
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manuscript
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PMID 39872516 full text
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data:geo:GSE115821
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GEO GSE115821
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pmid:39872516
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source:pmid:39872516
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PMID 39872516 full text
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GEO GSE115821
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agent:corpus-assay-engine
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agent:minimax-reader
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343fb30756ba6ec3
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[23]
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Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39872516", "kind": "science-record", "revision": 4, "content_hash": "sha256:d3432b6c4b7af9d45f4f51d53419e5a3375e897148e662cd1f2d3d13de403621", "created_at": "2026-11-01T20:30:09Z", "updated_at": "2026-11-01T22:56:03Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction of an anaplastic thyroid cancer stratification signature to guide immune therapy selection and validation of the pivotal gene HLF through in vitro experiments.", "doi": "10.3389/fimmu.2024.1478904", "pmid": "39872516", "authors": ["Li Pengping", "Yin Kexin", "Xie Yuwei", "Sun Ke", "Li Rongguo", "Wang Zhenyu", "Jin Haigang", "Wang Shaowen", "Huang Yuqing"], "journal": "Frontiers in immunology", "year": 2024, "abstract": "Introduction: While most thyroid cancer patients have a favorable prognosis, anaplastic thyroid carcinoma (ATC) remains a particularly aggressive form with a median survival time of just five months. Conventional therapies offer limited benefits for this type of thyroid cancer. Our study aims to identify ATC patients who might bene t from immunotherapy.\nMethods: Our study uses multiple algorithms by R4.2.0, and gene expression and clinical data are collected from TCGA, GEO and local cohort. In vitro experiments, such as western blot and immunofluorescence staining, are performed.\nResults: Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients (GSE60542, GSE76039, GSE33630, GSE53157, GSE65144, GSE29265, GSE82208, GSE27155, GSE58545, GSE54958, and GSE32662). These genes allowed us to stratify ATC into three distinct groups, each exhibiting significantly different responses to anti-PD1 therapy as determined by consensus clustering. Through weighted gene co-expression network analysis (WGCNA), we identified 12 differentially expressed genes closely associated with immunotherapy outcomes. This led to the creation of a refined signature for predicting ATC's immune responsiveness to anti-PD1 therapy, which was further validated using thyroid cancer cohorts from TCGA and nine melanoma cohorts from clinical trials. Among the 12 genes, HLF stood out due to its strong association with various cancer hallmarks.\nDiscussion: Our study revealed that HLF impedes ATC progression by down-regulating the epithelial-to-mesenchymal transition (EMT) pathway, reducing T cell exhaustion, and increasing sensitivity to sorafenib, as demonstrated through our in-vitro experiments.", "claims": [{"id": "claim-method", "statement": "Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39872516", "locator": "sections[10] \"The 12-gene signature construction\" paragraph 2", "quote": "Firstly, WGCNA (Weighted Gene Co-Expression Network Analysis) was applied to screen out hub genes using the WGCNA package in R4.2.0. The most correlated gene sets (both negative and positive) were collected for subsequent machine learning. AI modeling for ATC subgroup stratification was developed using six AI functions: extreme gradient boosting (XGboost, xgboost package in R4.2.0), support vector machine (SVM, e1071 packages in R4.2.0), multi-logistic (nnet packages in R4.2.0), random forest (RF, randomForest package in R4.2.0), deep learning (DL, h2o package in R4.2.0), and K-Nearest Neighbor (KNN, kknn package in R4.2.0)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39872516", "locator": "sections[34] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39872516", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients (GSE60542, GSE76039, GSE33630, GSE53157, GSE65144, GSE29265, GSE82208, GSE27155, GSE58545, GSE54958, and GSE32662)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "Using a set of five genes uniquely expressed across various types of thyroid cancer, we developed a machine-learning model to distinguish each type within the GEO dataset of thyroid cancer patients.", "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:39872516"], "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:GSE115821"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:machine_learning_random_forest", "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:GSE115821"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:machine_learning_random_forest"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39872516", "role": "manuscript", "format": "xml", "media_type": "application/xml", 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