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pmid:35483170

Identification of IMPA2 as the hub gene associated with colorectal cancer and liver metastasis by integrated bioinformatics analysis.

Liuli Wang · Deming Liu · Shuo Liu · Tianyi Liao · Yajun Jiao · Xianglai Jiang · Yongfeng Wang · Yaqiong Chen · Haizhong Ma · Hui Cai

Translational oncology · 2022 doi:10.1016/j.tranon.2022.101435

Paper

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title
Identification of IMPA2 as the hub gene associated with colorectal cancer and liver metastasis by integrated bioinformatics analysis.
doi
10.1016/j.tranon.2022.101435
pmid
35483170
authors array · 10 items
[0]
Liuli Wang
[1]
Deming Liu
[2]
Shuo Liu
[3]
Tianyi Liao
[4]
Yajun Jiao
[5]
Xianglai Jiang
[6]
Yongfeng Wang
[7]
Yaqiong Chen
[8]
Haizhong Ma
[9]
Hui Cai
journal
Translational oncology
year
2022
abstract
BACKGROUND AND OBJECTIVES: Colorectal cancer (CRC) is one of the most common malignant tumors worldwide with high incidence and mortality rate, while colorectal liver metastasis (CRLM) is one of the major causes of cancer-related deaths. Therefore, the present study aims to identify the hub gene associated with CRC carcinogenesis and liver metastasis, and then explore its diagnostic and prognostic value as well as the potential regulation mechanism. METHODS: The overlapping differential co-expression genes among CRC, CRLM, and normal tissues were explored on the GSE49355 and GSE81582 datasets from the Gene Expression Omnibus (GEO) database by integrated bioinformatics analysis. Then, the hub prognostic genes were selected from the overlapping genes by univariate Cox proportional hazard analysis and online database Gene Expression Profiling Interactive Analysis 2 (GEPIA2). Subsequently, the clinical value of the hub genes was evaluated in the TCGA and GSE39582 cohorts. Finally, the underlying mechanisms of the hub gene regulating CRC carcinogenesis and metastasis were explored by Gene function annotation and DNA methylation analysis. RESULTS: Inositol mono-phosphatase 2 (IMPA2) was identified as the hub gene associated with CRC carcinogenesis and liver metastasis. IMPA2 had an excellent diagnostic efficiency, and its expression was significantly decreased in CRC and liver metastasis samples, being positively correlated with poor prognosis. Moreover, its low expression was associated with AJCC stage III+IV, T4, N1+2, and M1. In addition, our results revealed that the potential mechanisms used by IMPA2 to mediate CRC carcinogenesis and metastasis could be associated with lipid metabolism and epithelial mesenchymal transition (EMT). Finally, IMPA2 expression could be regulated by DNA methylation. CONCLUSIONS: IMPA2 was identified and reported for the first time as a hub gene biomarker in the diagnosis and prognosis of CRC, which could regulate CRC carcinogenesis and liver metastasis through the regulation of lipid metabolism, EMT, and DNA methylation.
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Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
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Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
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The overlapping differential co-expression genes among CRC, CRLM, and normal tissues were explored on the GSE49355 and GSE81582 datasets from the Gene Expression Omnibus (GEO) database by integrated bioinformatics analysis.
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The overlapping differential co-expression genes among CRC, CRLM, and normal tissues were explored on the GSE49355 and GSE81582 datasets from the Gene Expression Omnibus (GEO) database by integrated bioinformatics analysis.
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The overlapping differential co-expression genes among CRC, CRLM, and normal tissues were explored on the GSE49355 and GSE81582 datasets from the Gene Expression Omnibus (GEO) database by integrated bioinformatics analysis.
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sample_count
585
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE41258
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=GSE41258
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE41258
version
null
note
Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
access_statement_kind
repository_route_statement
sample_accessions array · 390 items
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Homo sapiens
title
Expression data from colorectal cancer patients
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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[4] object · 15 fields
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Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
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57
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null
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96
taxon
Homo sapiens
title
Specific extracellular matrix remodeling signature of colon hepatic metastases [HG-U133A]
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
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data:geo:GSE81582
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Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
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102
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null
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null
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16384;15207
taxon
synthetic construct; Homo sapiens
title
Genomic characterization of liver metastases from colorectal cancer patients
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2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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complete
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Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);
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The paper names GSE49355, GSE81582, GSE39582, GSE41258, GSE17536 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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set and data processing Gene expression raw microarray profiles of CRC were evaluated in five indep
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35483170", "kind": "science-record", "revision": 4, "content_hash": "sha256:20044a3d421da92254bd86f3080aeda06666e85178f423bac3c6c92afc25f1cf", "created_at": "2026-11-01T18:14:21Z", "updated_at": "2026-11-01T22:06:25Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of IMPA2 as the hub gene associated with colorectal cancer and liver metastasis by integrated bioinformatics analysis.", "doi": "10.1016/j.tranon.2022.101435", "pmid": "35483170", "authors": ["Liuli Wang", "Deming Liu", "Shuo Liu", "Tianyi Liao", "Yajun Jiao", "Xianglai Jiang", "Yongfeng Wang", "Yaqiong Chen", "Haizhong Ma", "Hui Cai"], "journal": "Translational oncology", "year": 2022, "abstract": "BACKGROUND AND OBJECTIVES: Colorectal cancer (CRC) is one of the most common malignant tumors worldwide with high incidence and mortality rate, while colorectal liver metastasis (CRLM) is one of the major causes of cancer-related deaths. Therefore, the present study aims to identify the hub gene associated with CRC carcinogenesis and liver metastasis, and then explore its diagnostic and prognostic value as well as the potential regulation mechanism.\nMETHODS: The overlapping differential co-expression genes among CRC, CRLM, and normal tissues were explored on the GSE49355 and GSE81582 datasets from the Gene Expression Omnibus (GEO) database by integrated bioinformatics analysis. Then, the hub prognostic genes were selected from the overlapping genes by univariate Cox proportional hazard analysis and online database Gene Expression Profiling Interactive Analysis 2 (GEPIA2). Subsequently, the clinical value of the hub genes was evaluated in the TCGA and GSE39582 cohorts. Finally, the underlying mechanisms of the hub gene regulating CRC carcinogenesis and metastasis were explored by Gene function annotation and DNA methylation analysis.\nRESULTS: Inositol mono-phosphatase 2 (IMPA2) was identified as the hub gene associated with CRC carcinogenesis and liver metastasis. IMPA2 had an excellent diagnostic efficiency, and its expression was significantly decreased in CRC and liver metastasis samples, being positively correlated with poor prognosis. Moreover, its low expression was associated with AJCC stage III+IV, T4, N1+2, and M1. In addition, our results revealed that the potential mechanisms used by IMPA2 to mediate CRC carcinogenesis and metastasis could be associated with lipid metabolism and epithelial mesenchymal transition (EMT). Finally, IMPA2 expression could be regulated by DNA methylation.\nCONCLUSIONS: IMPA2 was identified and reported for the first time as a hub gene biomarker in the diagnosis and prognosis of CRC, which could regulate CRC carcinogenesis and liver metastasis through the regulation of lipid metabolism, EMT, and DNA methylation.", "claims": [{"id": "claim-data-access", "statement": "Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). GSE49355 included 57 samples (19 CRLM, 20 primary CRC and 18 normal tissues);", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35483170", "locator": "sections[3] \"GEO data set and data processing\" paragraph 2", "quote": "Gene expression raw microarray profiles of CRC were evaluated in five independent datasets (accession nos. GSE49355 [15], GSE81582 [16], GSE39582 [17], GSE41258 [18], and GSE17536 [19]) from the GEO database (www.ncbi.nlm.nih.gov/geo). 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