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pmid:34332578

Quantification of m6A RNA methylation modulators pattern was a potential biomarker for prognosis and associated with tumor immune microenvironment of pancreatic adenocarcinoma.

Lianzi Wang · Shubing Zhang · Huimin Li · Yang Xu · Qiang Wu · Jilong Shen · Tao Li · Yuanhong Xu

BMC cancer · 2021 doi:10.1186/s12885-021-08550-9

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:34332578
kind
science-record
content_hash
sha256:1bb44f99107bc33c70689579bd039293ff4e6b49903427de59ae1227121531b9
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:41:46Z
updated_at
2026-11-01T22:04:22Z
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paper object · 10 fields
state
complete
title
Quantification of m6A RNA methylation modulators pattern was a potential biomarker for prognosis and associated with tumor immune microenvironment of pancreatic adenocarcinoma.
doi
10.1186/s12885-021-08550-9
pmid
34332578
authors array · 8 items
[0]
Lianzi Wang
[1]
Shubing Zhang
[2]
Huimin Li
[3]
Yang Xu
[4]
Qiang Wu
[5]
Jilong Shen
[6]
Tao Li
[7]
Yuanhong Xu
journal
BMC cancer
year
2021
abstract
BACKGROUND: m6A is the most prevalent and abundant form of mRNA modifications and is closely related to tumor proliferation, differentiation, and tumorigenesis. In this study, we try to conduct an effective prediction model to investigated the function of m6A RNA methylation modulators in pancreatic adenocarcinoma and estimated the potential association between m6A RNA methylation modulators and tumor microenvironment infiltration for optimization of treatment. METHODS: Expression of 28 m6A RNA methylation modulators and clinical data of patients with pancreatic adenocarcinoma and normal samples were obtained from TCGA and GTEx database. Differences in the expression of 28 m6A RNA methylation modulators between tumour (n = 40) and healthy (n = 167) samples were compared by Wilcoxon test. LASSO Cox regression was used to select m6A RNA methylation modulators to analyze the relationship between expression and clinical characteristics by univariate and multivariate regression. A risk score prognosis model was conducted based on the expression of select m6A RNA methylation modulators. Bioinformatics analysis was used to explore the association between the m6Ascore and the composition of infiltrating immune cells between high and low m6Ascore group by CIBERSORT algorithm. Evaluation of m6Ascore for immunotherapy was analyzed via the IPS and three immunotherapy cohort. Besides, the biological signaling pathways of the m6A RNA methylation modulators were examined by gene set enrichment analysis (GSEA). RESULTS: Expression of 28 m6A RNA methylation modulators were upregulated in patients with PAAD except for MTEEL3. An m6Ascore prognosis model was established, including KIAA1429, IGF2BP2, IGF2BP3, METTL3, EIF3H and LRPPRC was used to predict the prognosis of patients with PAAD, the high risk score was an independent prognostic indicator for pancreatic adenocarcinoma, and a high risk score presented a lower overall survival. In addition, m6Ascore was related with the immune cell infiltration of PAAD. Patients with a high m6Ascore had lower infiltration of Tregs and CD8+T cells but a higher resting CD4+ T infiltration. Patients with a low m6Ascore displayed a low abundance of PD-1, CTLA-4 and TIGIT, however, the IPS showed no difference between the two groups. The m6Ascore applied in three immunotherapy cohort (GSE78220, TCGA-SKCM, and IMvigor210) did not exhibit a good prediction for estimating the patients' response to immunotherapy, so it may need more researches to figure out whether the m6A modulator prognosis model would benefit the prediction of pancreatic patients' response to immunotherapy. CONCLUSION: Modulators involved in m6A RNA methylation were associated with the development of pancreatic cancer. An m6Ascore based on the expression of IGF2BP2, IGF2BP3, KIAA1429, METTL3, EIF3H and LRPPRC is proposed as an indicator of TME status and is instrumental in predicting the prognosis of pancreatic cancer patients.
claims array · 2 items
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claim-method
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Cox regression analysis was used to examine the prognosis of pancreatic cancer.
kind
methodological
target
null
evidence array · 1 item
[0] object · 3 fields
asset
source:pmid:34332578
locator
sections[11] "Statistical analysis" paragraph 2
quote
Cox regression analysis was used to examine the prognosis of pancreatic cancer.
state
complete
[1] object · 6 fields
id
claim-data-access
statement
The datasets analyzed during the current study are available from TCGA database (https://cancergenome.nih.gov/), GTEx database (https://xenabrowser.net/), Immport database (https://immport.niaid.nih.gov/), TCIA database (https://www.tcia.at/home), GEO database (https://www.ncbi.nlm.nih.gov/geo/), Oncomine database (https://www.oncomine.org).
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null
evidence array · 1 item
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sections[26] "Availability of data and materials" paragraph 2
quote
The datasets analyzed during the current study are available from TCGA database (https://cancergenome.nih.gov/), GTEx database (https://xenabrowser.net/), Immport database (https://immport.niaid.nih.gov/), TCIA database (https://www.tcia.at/home), GEO database (https://www.ncbi.nlm.nih.gov/geo/), Oncomine database (https://www.oncomine.org).
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Read the published estimate from the source
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The claim, method and evidence span published with the source article.
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the published estimate and its evidence
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Obtain the source data from the named repository
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The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.
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the source data with its repository provenance
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Run the published analysis
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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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https://doi.org/10.1186/s12885-021-08550-9
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PMC8325189
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the lists of the 28 m6A RNA methylation regulative factors
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PMC8325189
section_index
4
section_title
Extraction of m6A RNA methylation modulator expression data
row_count
29
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3
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label
Table 1
caption
the lists of the 28 m6A RNA methylation regulative factors
rows array · 29 items
[0] array · 3 items
[0]
Regulators
[1]
Full name
[2]
Type
[1] array · 3 items
[0]
METTL3
[1]
Methyltransferase like 3
[2]
“writers”
[2] array · 3 items
[0]
METTL14
[1]
Methyltransferase like 14
[2]
“writers”
[3] array · 3 items
[0]
METTL16
[1]
Methyltransferase like 16
[2]
“writers”
[4] array · 3 items
[0]
WTAP
[1]
WT1 associated protein
[2]
“writers”
[5] array · 3 items
[0]
RBM15
[1]
RNA binding motif protein 15
[2]
“writers”
[6] array · 3 items
[0]
RBM15B
[1]
RNA binding motif protein 15B
[2]
“writers”
[7] array · 3 items
[0]
ZC3H13
[1]
Zinc finger CCCH-type containing 13
[2]
“writers”
[8] array · 3 items
[0]
VIRMA
[1]
vir like m6A methyltransferase associated
[2]
“writers”
[9] array · 3 items
[0]
CBLL1
[1]
Cbl proto-oncogene like 1
[2]
“writers”
[10] array · 3 items
[0]
ZCCHC4
[1]
zinc finger CCHC-type containing 4
[2]
“writers”
[11] array · 3 items
[0]
LRPPRC
[1]
leucine rich pentatricopeptide repeat containing
[2]
“readers”
[12] array · 3 items
[0]
ELAVL1
[1]
ELAV like RNA binding protein 1
[2]
“readers”
[13] array · 3 items
[0]
YTHDC1
[1]
YTH domain containing 1
[2]
“readers”
[14] array · 3 items
[0]
YTHDC2
[1]
YTH domain containing 2
[2]
“readers”
[15] array · 3 items
[0]
YTHDF1
[1]
YTH N6-methyladenosine RNA binding protein 1
[2]
“readers”
[16] array · 3 items
[0]
YTHDF2
[1]
YTH N6-methyladenosine RNA binding protein 2
[2]
“readers”
[17] array · 3 items
[0]
YTHDF3
[1]
YTH N6-methyladenosine RNA binding protein 3
[2]
“readers”
[18] array · 3 items
[0]
HNRNPC
[1]
Heterogeneous nuclear ribonucleoprotein C
[2]
“readers”
[19] array · 3 items
[0]
HNRNPA2B1
[1]
Heterogeneous nuclear ribonucleoprotein A2B1
[2]
“readers”
[20] array · 3 items
[0]
EIF3A
[1]
Eukaryotic translation initiation factor 3 subunit A
[2]
“readers”
[21] array · 3 items
[0]
EIF3H
[1]
Eukaryotic translation initiation factor 3 subunit H
[2]
“readers”
[22] array · 3 items
[0]
IGF2BP1
[1]
IGF2 mRNA-binding protein 1
[2]
“readers”
[23] array · 3 items
[0]
IGF2BP2
[1]
IGF2 mRNA-binding protein 2
[2]
“readers”
[24] array · 3 items
[0]
IGF2BP3
[1]
IGF2 mRNA-binding protein 3
[2]
“readers”
[25] array · 3 items
[0]
CBLL1
[1]
Casitas B-lineage lymphoma-transforming sequence-like protein 1
[2]
“readers”
[26] array · 3 items
[0]
PRRC2A
[1]
The proline-rich coiled-coil 2A
[2]
“readers”
[27] array · 3 items
[0]
FTO
[1]
Fat mass and obesity-associated protein
[2]
“erasers”
[28] array · 3 items
[0]
ALKBH5
[1]
α-ketoglutarate-dependent dioxygenase AlkB homolog 5
[2]
“erasers”
locator
section[4]/table-wrap[1]#Tab1
[2] object · 16 fields
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Demographic and clinicopathological parameters of PAAD patients based on TCGA datasets
structure object · 5 fields
pmcid
PMC8325189
section_index
14
section_title
m6A RNA methylation modulators were associated with clinical characteristic of PAAD
row_count
49
column_count
5
table object · 8 fields
label
Table 2
caption
Demographic and clinicopathological parameters of PAAD patients based on TCGA datasets
rows array · 49 items
[0] array · 5 items
[0]
Clinical characteristics
[1]
All
[2]
High m6Ascore
[3]
low m6Ascore
[4]
P value
[1] array · 5 items
[0]
Age
[1]
64.54 ± 10.81
[2]
63.74 ± 11.68
[3]
65.33 ± 9.88
[4]
0.387
[2] array · 5 items
[0]
Gender
[1]
[2]
[3]
[4]
0.735
[3] array · 5 items
[0]
Female
[1]
66
[2]
34
[3]
32
[4]
[4] array · 5 items
[0]
Male
[1]
74
[2]
36
[3]
38
[4]
[5] array · 5 items
[0]
Race
[1]
[2]
[3]
[4]
0.689
[6] array · 5 items
[0]
Asian
[1]
8
[2]
5
[3]
3
[4]
[7] array · 5 items
[0]
White
[1]
123
[2]
60
[3]
63
[4]
[8] array · 5 items
[0]
Black or African American
[1]
5
[2]
2
[3]
3
[4]
[9] array · 5 items
[0]
Fustat
[1]
[2]
[3]
[4]
< 0.001
[10] array · 5 items
[0]
Living
[1]
63
[2]
21
[3]
42
[4]
[11] array · 5 items
[0]
Deceased
[1]
77
[2]
49
[3]
28
[4]
[12] array · 5 items
[0]
Pathologic stage
[1]
[2]
[3]
[4]
0.927
[13] array · 5 items
[0]
I (IA + IB)
[1]
12
[2]
6
[3]
6
[4]
[14] array · 5 items
[0]
II (IIA + IIB)
[1]
121
[2]
60
[3]
61
[4]
[15] array · 5 items
[0]
III+ IV
[1]
7
[2]
4
[3]
3
[4]
[16] array · 5 items
[0]
T
[1]
[2]
[3]
[4]
0.813
[17] array · 5 items
[0]
T1+ T2
[1]
21
[2]
10
[3]
11
[4]
[18] array · 5 items
[0]
T3 + T4
[1]
119
[2]
60
[3]
59
[4]
[19] array · 5 items
[0]
M
[1]
[2]
[3]
[4]
0.361
[20] array · 5 items
[0]
M0
[1]
66
[2]
34
[3]
32
[4]
[21] array · 5 items
[0]
M1
[1]
4
[2]
3
[3]
1
[4]
[22] array · 5 items
[0]
N
[1]
[2]
[3]
[4]
0.808
[23] array · 5 items
[0]
N0
[1]
37
[2]
19
[3]
18
[4]
[24] array · 5 items
[0]
N1(N1a + N1b)
[1]
102
[2]
50
[3]
52
[4]
[25] array · 5 items
[0]
Histologic grade
[1]
[2]
[3]
[4]
0.140
[26] array · 5 items
[0]
G1-G2
[1]
98
[2]
45
[3]
53
[4]
[27] array · 5 items
[0]
G3-G4
[1]
42
[2]
25
[3]
17
[4]
[28] array · 1 item
[0]
Site
[29] array · 5 items
[0]
Head of pancreas
[1]
110
[2]
54
[3]
56
[4]
0.139
[30] array · 5 items
[0]
Body of pancreas
[1]
11
[2]
8
[3]
3
[4]
[31] array · 5 items
[0]
Tail of pancreas
[1]
10
[2]
6
[3]
4
[4]
[32] array · 5 items
[0]
others
[1]
9
[2]
2
[3]
7
[4]
[33] array · 5 items
[0]
Maximum tumor dimension
[1]
3.75 ± 1.44
[2]
4.05 ± 1.72
[3]
3.42 ± 0.98
[4]
0.013
[34] array · 5 items
[0]
History of targeted molecular therapy
[1]
[2]
[3]
[4]
0.185
[35] array · 5 items
[0]
YES
[1]
75
[2]
37
[3]
38
[4]
[36] array · 5 items
[0]
NO
[1]
35
[2]
22
[3]
13
[4]
[37] array · 5 items
[0]
Alcohol drinking history
[1]
[2]
[3]
[4]
0.910
[38] array · 5 items
[0]
YES
[1]
80
[2]
40
[3]
40
[4]
[39] array · 5 items
[0]
NO
[1]
49
[2]
24
[3]
25
[4]
[40] array · 5 items
[0]
History of chronic pancreatitis
[1]
[2]
[3]
[4]
0.726
[41] array · 5 items
[0]
YES
[1]
12
[2]
7
[3]
5
[4]
[42] array · 5 items
[0]
NO
[1]
100
[2]
53
[3]
47
[4]
[43] array · 5 items
[0]
History of diabetes
[1]
[2]
[3]
[4]
0.157
[44] array · 5 items
[0]
YES
[1]
32
[2]
13
[3]
19
[4]
[45] array · 5 items
[0]
NO
[1]
85
[2]
47
[3]
38
[4]
[46] array · 5 items
[0]
Family history of cancer
[1]
[2]
[3]
[4]
0.910
[47] array · 5 items
[0]
YES
[1]
50
[2]
21
[3]
29
[4]
[48] array · 5 items
[0]
NO
[1]
33
[2]
23
[3]
10
[4]
locator
section[14]/table-wrap[1]#Tab2
[3] object · 16 fields
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Association between the expression of eight m6A RNA methylation modulators and clinical characteristic in patients with PAAD based on the TCGA datasets
structure object · 5 fields
pmcid
PMC8325189
section_index
14
section_title
m6A RNA methylation modulators were associated with clinical characteristic of PAAD
row_count
20
column_count
13
table object · 8 fields
label
Table 3
caption
Association between the expression of eight m6A RNA methylation modulators and clinical characteristic in patients with PAAD based on the TCGA datasets
rows array · 20 items
[0] array · 7 items
[0]
[1]
EIF3H
[2]
IGF2BP3
[3]
IGF2BP2
[4]
KIAA1429
[5]
METTL3
[6]
LRPPRC
[1] array · 12 items
[0]
down expression
[1]
overexpression
[2]
down expression
[3]
overexpression
[4]
down expression
[5]
overexpression
[6]
down expression
[7]
overexpression
[8]
down expression
[9]
overexpression
[10]
down expression
[11]
overexpression
[2] array · 13 items
[0]
N
[1]
70
[2]
70
[3]
70
[4]
70
[5]
70
[6]
70
[7]
70
[8]
70
[9]
70
[10]
70
[11]
70
[12]
70
[3] array · 13 items
[0]
Age
[1]
64.54 ± 10.77
[2]
64.53 ± 10.92
[3]
66.57 ± 9.71
[4]
62.50 ± 11.51
[5]
67.46 ± 9.92
[6]
61.61 ± 10.93
[7]
65.51 ± 10.68
[8]
63.56 ± 10.92
[9]
65.77 ± 10.62
[10]
63.30 ± 10.93
[11]
64.66 ± 10.42
[12]
64.41 ± 11.26
[4] array · 13 items
[0]
P-value
[1]
0.994
[2]
[3]
0.025
[4]
[5]
0.001
[6]
[7]
0.286
[8]
[9]
0.177
[10]
[11]
0.895
[12]
[5] array · 1 item
[0]
Gender
[6] array · 13 items
[0]
female
[1]
33 (47.14%)
[2]
33 (47.14%)
[3]
35 (50.00%)
[4]
31 (44.29%)
[5]
39 (55.71%)
[6]
27 (38.57%)
[7]
27 (38.57%)
[8]
39 (55.71%)
[9]
35 (50.00%)
[10]
31 (44.29%)
[11]
31 (44.29%)
[12]
35 (50.00%)
[7] array · 13 items
[0]
male
[1]
37 (52.86%)
[2]
37 (52.86%)
[3]
35 (50.00%)
[4]
39 (55.71%)
[5]
31 (44.29%)
[6]
43 (61.43%)
[7]
43 (61.43%)
[8]
31 (44.29%)
[9]
35 (50.00%)
[10]
39 (55.71%)
[11]
39 (55.71%)
[12]
35 (50.00%)
[8] array · 13 items
[0]
P-value
[1]
1.000
[2]
[3]
0.498
[4]
[5]
0.042
[6]
[7]
0.042
[8]
[9]
0.498
[10]
[11]
0.498
[12]
[9] array · 13 items
[0]
Maximum tumor dimension
[1]
3.44 ± 1.03
[2]
4.04 ± 1.70
[3]
3.40 ± 0.96
[4]
4.10 ± 1.74
[5]
3.37 ± 0.95
[6]
4.15 ± 1.74
[7]
3.79 ± 1.57
[8]
3.71 ± 1.30
[9]
3.52 ± 1.14
[10]
3.98 ± 1.68
[11]
3.49 ± 1.07
[12]
3.99 ± 1.69
[10] array · 13 items
[0]
P-value
[1]
0.016
[2]
[3]
0.006
[4]
[5]
0.002
[6]
[7]
0.755
[8]
[9]
0.069
[10]
[11]
0.050
[12]
[11] array · 1 item
[0]
Stage
[12] array · 13 items
[0]
StagI (IA + IB)
[1]
6 (8.57%)
[2]
6 (8.57%)
[3]
8 (11.43%)
[4]
4 (5.71%)
[5]
8 (11.43%)
[6]
4 (5.71%)
[7]
4 (5.71%)
[8]
8 (11.43%)
[9]
7 (10.00%)
[10]
5 (7.14%)
[11]
6 (8.57%)
[12]
6 (8.57%)
[13] array · 13 items
[0]
StagII (IIA + IIB)
[1]
62 (88.57%)
[2]
59 (84.29%)
[3]
59 (84.29%)
[4]
62 (88.57%)
[5]
59 (84.29%)
[6]
62 (88.57%)
[7]
62 (88.57%)
[8]
59 (84.29%)
[9]
58 (82.86%)
[10]
63 (90.00%)
[11]
60 (85.71%)
[12]
61 (87.14%)
[14] array · 13 items
[0]
StagIII+IV
[1]
2 (2.86%)
[2]
5 (7.14%)
[3]
3 (4.29%)
[4]
4 (5.71%)
[5]
3 (4.29%)
[6]
4 (5.71%)
[7]
4 (5.71%)
[8]
3 (4.29%)
[9]
5 (7.14%)
[10]
2 (2.86%)
[11]
4 (5.71%)
[12]
3 (4.29%)
[15] array · 13 items
[0]
P-value
[1]
0.507
[2]
[3]
0.461
[4]
[5]
0.461
[6]
[7]
0.461
[8]
[9]
0.401
[10]
[11]
0.927
[12]
[16] array · 1 item
[0]
Grade
[17] array · 13 items
[0]
G1 + G2
[1]
51 (72.86%)
[2]
47 (67.14%)
[3]
51 (72.86%)
[4]
47 (67.14%)
[5]
59 (84.29%)
[6]
39 (55.71%)
[7]
52 (74.29%)
[8]
46 (65.71%)
[9]
52 (74.29%)
[10]
46 (65.71%)
[11]
55 (78.57%)
[12]
43 (61.43%)
[18] array · 13 items
[0]
G3 + G4
[1]
19 (27.14%)
[2]
23 (32.86%)
[3]
19 (27.14%)
[4]
23 (32.86%)
[5]
11 (15.71%)
[6]
31 (44.29%)
[7]
18 (25.71%)
[8]
24 (34.29%)
[9]
18 (25.71%)
[10]
24 (34.29%)
[11]
15 (21.43%)
[12]
27 (38.57%)
[19] array · 13 items
[0]
P-value
[1]
0.461
[2]
[3]
0.461
[4]
[5]
< 0.001
[6]
[7]
0.268
[8]
[9]
0.268
[10]
[11]
0.027
[12]
locator
section[14]/table-wrap[2]#Tab3
[4] object · 16 fields
id
asset:table:pmid:34332578:4
role
table
format
jats-table
media_type
application/vnd.jats.table+json
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sha256
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bytes
616
access
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verified
reader
read_table
reader_status
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identifier
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version
null
note
gene set enrichment analysis for six m6A modulators with KEGG pathway using GSEA
structure object · 5 fields
pmcid
PMC8325189
section_index
16
section_title
The function analysis and the pathways of the genes that enriched in the group of PAAD patients with high-risk and low-risk
row_count
6
column_count
6
table object · 8 fields
label
Table 4
caption
gene set enrichment analysis for six m6A modulators with KEGG pathway using GSEA
rows array · 6 items
[0] array · 6 items
[0]
Gene name
[1]
KEGG pathway
[2]
ES
[3]
NES
[4]
NOM p-val
[5]
FDR q-val
[1] array · 6 items
[0]
EIF3H
[1]
KEGG_CELL_CYCLE
[2]
0.73
[3]
2.1
[4]
0.000
[5]
0.003
[2] array · 6 items
[0]
IGF2BP2
[1]
KEGG_BLADDER_ CANCER
[2]
0.68
[3]
2.07
[4]
0.000
[5]
0.007
[3] array · 6 items
[0]
IGF2BP3
[1]
KEGG_PANCREATIC_CANCER
[2]
0.65
[3]
1.93
[4]
0.000
[5]
0.006
[4] array · 6 items
[0]
LRPPRC
[1]
KEGG_PANCREATIC_CANCER
[2]
0.71
[3]
2.06
[4]
0.000
[5]
0.001
[5] array · 6 items
[0]
VIRMA
[1]
KEGG_PATHWAYS IN _CANCER
[2]
0.64
[3]
2.13
[4]
0.000
[5]
0.001
locator
section[16]/table-wrap[1]#Tab4
gaps array · 0 items
analysis object · 4 fields
state
partial
methods array · 7 items
[0] object · 10 fields
id
method-1
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survival_analysis
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cox_proportional_hazards
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Survival analysis
dsl_operations array · 1 item
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cox_ph
missing_operations array · 0 items
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data_shapes array · 1 item
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time_to_event_with_censoring
evidence object · 3 fields
score
1
band
verbatim
quote
Cox regression analysis was used to examine the prognosis of pancreatic cancer.
[1] object · 10 fields
id
method-2
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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 · 1 field
sample_size
ulators between tumour (n = 40) and healthy (n = 167)
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.7
band
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Wilcoxon
[2] object · 10 fields
id
method-3
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survival_analysis
specific
kaplan_meier
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Survival analysis
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[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
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time_to_event_with_censoring
evidence object · 3 fields
score
0.8
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Kaplan-Meier
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id
method-4
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regression_modelling
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ols
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Regression modelling
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ols_fit
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
predictors_and_outcome
evidence object · 3 fields
score
0.8
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Multiple regression
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id
method-5
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network_analysis
specific
pathway_enrichment
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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
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edge_list
evidence object · 3 fields
score
0.8
band
high
quote
pathway enrichment
[5] object · 10 fields
id
method-6
family
diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
dsl_operations array · 6 items
[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
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solve_confusion_matrix
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classification_metrics
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published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
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reference_standard_and_test
evidence object · 3 fields
score
0.8
band
high
quote
ROC analysis
[6] object · 10 fields
id
method-7
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
dsl_operations array · 1 item
[0]
chi_square_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
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categorical_cross_tabulation
evidence object · 3 fields
score
0.8
band
high
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Chi-square
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gaps array · 1 item
[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
complete
requirements array · 1 item
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capability_id
capability:computational_analysis
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assay_families array · 9 items
[0]
meta_analysis
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machine_learning
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survival_analysis
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statistical_regression
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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
blocked
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R4
blocked_on
data:accession_absent
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 1 item
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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
R4
reachable
false
accessions array · 0 items
resolved_accessions array · 0 items
statements array · 1 item
[0]
The datasets analyzed during the current study are available from TCGA database (https://cancergenome.nih.gov/), GTEx database (https://xenabrowser.net/), Immport database (https://immport.niaid.nih.gov/), TCIA database (https://www.tcia.at/home), GEO database (https://www.ncbi.nlm.nih.gov/geo/), Oncomine database (https://www.oncomine.org).
basis
The paper names no accession to its source data, so the data has to come from the authors.
can_run object · 3 fields
dsl_operations array · 1 item
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cox_ph
assets array · 5 items
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source:pmid:34332578
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asset:table:pmid:34332578:3
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asset:table:pmid:34332578:4
steps array · 1 item
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run_analysis
must_build object · 5 fields
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
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gaps array · 1 item
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data:accession_absent
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
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model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
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single_reader
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method
verbatim
availability
verbatim
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3
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51124
completion_tokens
3101
cached_tokens
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id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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review.machine_critique
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review.human_critique
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not_run
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execution.not_run
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pmid:34332578
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paper
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pmid:34332578
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source:pmid:34332578
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manuscript
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data:geo:None
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dataset
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source:pmid:34332578
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agent:corpus-assay-engine
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supported
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dsl_catalogue
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Cox regression analysis was used to examine the prognosis of pancreatic cancer.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34332578", "kind": "science-record", "revision": 7, "content_hash": "sha256:1bb44f99107bc33c70689579bd039293ff4e6b49903427de59ae1227121531b9", "created_at": "2026-11-01T15:41:46Z", "updated_at": "2026-11-01T22:04:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Quantification of m6A RNA methylation modulators pattern was a potential biomarker for prognosis and associated with tumor immune microenvironment of pancreatic adenocarcinoma.", "doi": "10.1186/s12885-021-08550-9", "pmid": "34332578", "authors": ["Lianzi Wang", "Shubing Zhang", "Huimin Li", "Yang Xu", "Qiang Wu", "Jilong Shen", "Tao Li", "Yuanhong Xu"], "journal": "BMC cancer", "year": 2021, "abstract": "BACKGROUND: m6A is the most prevalent and abundant form of mRNA modifications and is closely related to tumor proliferation, differentiation, and tumorigenesis. In this study, we try to conduct an effective prediction model to investigated the function of m6A RNA methylation modulators in pancreatic adenocarcinoma and estimated the potential association between m6A RNA methylation modulators and tumor microenvironment infiltration for optimization of treatment.\nMETHODS: Expression of 28 m6A RNA methylation modulators and clinical data of patients with pancreatic adenocarcinoma and normal samples were obtained from TCGA and GTEx database. Differences in the expression of 28 m6A RNA methylation modulators between tumour (n = 40) and healthy (n = 167) samples were compared by Wilcoxon test. LASSO Cox regression was used to select m6A RNA methylation modulators to analyze the relationship between expression and clinical characteristics by univariate and multivariate regression. A risk score prognosis model was conducted based on the expression of select m6A RNA methylation modulators. Bioinformatics analysis was used to explore the association between the m6Ascore and the composition of infiltrating immune cells between high and low m6Ascore group by CIBERSORT algorithm. Evaluation of m6Ascore for immunotherapy was analyzed via the IPS and three immunotherapy cohort. Besides, the biological signaling pathways of the m6A RNA methylation modulators were examined by gene set enrichment analysis (GSEA).\nRESULTS: Expression of 28 m6A RNA methylation modulators were upregulated in patients with PAAD except for MTEEL3. An m6Ascore prognosis model was established, including KIAA1429, IGF2BP2, IGF2BP3, METTL3, EIF3H and LRPPRC was used to predict the prognosis of patients with PAAD, the high risk score was an independent prognostic indicator for pancreatic adenocarcinoma, and a high risk score presented a lower overall survival. In addition, m6Ascore was related with the immune cell infiltration of PAAD. Patients with a high m6Ascore had lower infiltration of Tregs and CD8+T cells but a higher resting CD4+ T infiltration. Patients with a low m6Ascore displayed a low abundance of PD-1, CTLA-4 and TIGIT, however, the IPS showed no difference between the two groups. The m6Ascore applied in three immunotherapy cohort (GSE78220, TCGA-SKCM, and IMvigor210) did not exhibit a good prediction for estimating the patients' response to immunotherapy, so it may need more researches to figure out whether the m6A modulator prognosis model would benefit the prediction of pancreatic patients' response to immunotherapy.\nCONCLUSION: Modulators involved in m6A RNA methylation were associated with the development of pancreatic cancer. An m6Ascore based on the expression of IGF2BP2, IGF2BP3, KIAA1429, METTL3, EIF3H and LRPPRC is proposed as an indicator of TME status and is instrumental in predicting the prognosis of pancreatic cancer patients.", "claims": [{"id": "claim-method", "statement": "Cox regression analysis was used to examine the prognosis of pancreatic cancer.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34332578", "locator": "sections[11] \"Statistical analysis\" paragraph 2", "quote": "Cox regression analysis was used to examine the prognosis of pancreatic cancer."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets analyzed during the current study are available from TCGA database (https://cancergenome.nih.gov/), GTEx database (https://xenabrowser.net/), Immport database (https://immport.niaid.nih.gov/), TCIA database (https://www.tcia.at/home), GEO database (https://www.ncbi.nlm.nih.gov/geo/), Oncomine database (https://www.oncomine.org).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34332578", "locator": "sections[26] \"Availability of data and materials\" paragraph 2", "quote": "The datasets analyzed during the current study are available from TCGA database (https://cancergenome.nih.gov/), GTEx database (https://xenabrowser.net/), Immport database (https://immport.niaid.nih.gov/), TCIA database (https://www.tcia.at/home), GEO database (https://www.ncbi.nlm.nih.gov/geo/), Oncomine database (https://www.oncomine.org)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": null, "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:34332578"], "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": "blocked", "blocked_on": "data:accession_absent", "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": [], "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": [], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:obtain_source_data blocked on data:accession_absent"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34332578", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12885-021-08550-9", "sha256": 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