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pmid:37076536

Prognostic model development for classification of colorectal adenocarcinoma by using machine learning model based on feature selection technique boruta.

Neha Shree Maurya · Shikha Kushwah · Sandeep Kushwaha · Aakash Chawade · Ashutosh Mani

Scientific reports · 2023 doi:10.1038/s41598-023-33327-4

Paper

complete

Experiment

complete

Data

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Analysis

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pmid:37076536
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title
Prognostic model development for classification of colorectal adenocarcinoma by using machine learning model based on feature selection technique boruta.
doi
10.1038/s41598-023-33327-4
pmid
37076536
authors array · 5 items
[0]
Neha Shree Maurya
[1]
Shikha Kushwah
[2]
Sandeep Kushwaha
[3]
Aakash Chawade
[4]
Ashutosh Mani
journal
Scientific reports
year
2023
abstract
Colorectal cancer (CRC) is the third most prevalent cancer type and accounts for nearly one million deaths worldwide. The CRC mRNA gene expression datasets from TCGA and GEO (GSE144259, GSE50760, and GSE87096) were analyzed to find the significant differentially expressed genes (DEGs). These significant genes were further processed for feature selection through boruta and the confirmed features of importance (genes) were subsequently used for ML-based prognostic classification model development. These genes were analyzed for survival and correlation analysis between final genes and infiltrated immunocytes. A total of 770 CRC samples were included having 78 normal and 692 tumor tissue samples. 170 significant DEGs were identified after DESeq2 analysis along with the topconfects R package. The 33 confirmed features of importance-based RF prognostic classification model have given accuracy, precision, recall, and f1-score of 100% with 0% standard deviation. The overall survival analysis had finalized GLP2R and VSTM2A genes that were significantly downregulated in tumor samples and had a strong correlation with immunocyte infiltration. The involvement of these genes in CRC prognosis was further confirmed on the basis of their biological function and literature analysis. The current findings indicate that GLP2R and VSTM2A may play a significant role in CRC progression and immune response suppression.
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Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5. The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package. To obtain a significant list of DEGs from GEO datasets "topconfects"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value.
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sections[13] "Identification of significant DEGs" paragraph 2
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Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5.
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The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package.
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sections[13] "Identification of significant DEGs" paragraph 4
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To obtain a significant list of DEGs from GEO datasets "topconfects"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value.
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Publicly available dataset was used analyzed which are available on the TCGA repository site (https://portal.gdc.cancer.gov/) with project name TCGA-COAD and TCGA-READ and GEO site (https://www.ncbi.nlm.nih.gov/geo/). The accession number for the GEO datasets are (a) GSE144259, (b) GSE50760, and (c) GSE87096.
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Publicly available dataset was used analyzed which are available on the TCGA repository site (https://portal.gdc.cancer.gov/) with project name TCGA-COAD and TCGA-READ and GEO site (https://www.ncbi.nlm.nih.gov/geo/). The accession number for the GEO datasets are (a) GSE144259, (b) GSE50760, and (c) GSE87096.
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A total of 170 significant common DEGs were found between 3 GEO datasets and the TCGA-CRC dataset.
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sections[4] "Identification of significant DEGs" paragraph 4
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A total of 170 significant common DEGs were found between 3 GEO datasets and the TCGA-CRC dataset as shown in Fig. 3.
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170 significant DEGs were identified after DESeq2 analysis along with the topconfects R package.
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A total of 170 significant common DEGs were found between 3 GEO datasets and the TCGA-CRC dataset.
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Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5. The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package. To obtain a significant list of DEGs from GEO datasets "topconfects"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value.
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Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5. The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package. To obtain a significant list of DEGs from GEO datasets "topconfects"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value.
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Complete file
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The CRC mRNA gene expression datasets from TCGA and GEO (GSE144259, GSE50760, and GSE87096) were analyzed to find the significant differentially expressed genes (DEGs). These significant genes were further processed for feature selection through boruta and the confirmed features of importance (genes) were subsequently used for ML-based prognostic classification model development. These genes were analyzed for survival and correlation analysis between final genes and infiltrated immunocytes. A total of 770 CRC samples were included having 78 normal and 692 tumor tissue samples. 170 significant DEGs were identified after DESeq2 analysis along with the topconfects R package. The 33 confirmed features of importance-based RF prognostic classification model have given accuracy, precision, recall, and f1-score of 100% with 0% standard deviation. The overall survival analysis had finalized GLP2R and VSTM2A genes that were significantly downregulated in tumor samples and had a strong correlation with immunocyte infiltration. The involvement of these genes in CRC prognosis was further confirmed on the basis of their biological function and literature analysis. The current findings indicate that GLP2R and VSTM2A may play a significant role in CRC progression and immune response suppression.", "claims": [{"id": "claim-method", "statement": "Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5. The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package. To obtain a significant list of DEGs from GEO datasets \"topconfects\"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37076536", "locator": "sections[13] \"Identification of significant DEGs\" paragraph 2", "quote": "Thereafter, the threshold implemented to identify the DEGs between normal and CRC tumor samples using the edgeR by glmRT method was FDR cut-off of 0.01 and |log 2‐FC|> 1.5."}, {"asset": "source:pmid:37076536", "locator": "sections[13] \"Identification of significant DEGs\" paragraph 3", "quote": "The gene expression count data for GEO datasets were processed through DESeq217 R Bioconductor package."}, {"asset": "source:pmid:37076536", "locator": "sections[13] \"Identification of significant DEGs\" paragraph 4", "quote": "To obtain a significant list of DEGs from GEO datasets \"topconfects\"18 Bioconductor R package was employed which ranks the genes based on the confidence score bound to log fold change value."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available dataset was used analyzed which are available on the TCGA repository site (https://portal.gdc.cancer.gov/) with project name TCGA-COAD and TCGA-READ and GEO site (https://www.ncbi.nlm.nih.gov/geo/). 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