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pmid:38773226

Anoikis-related gene signatures in colorectal cancer: implications for cell differentiation, immune infiltration, and prognostic prediction.

Taohui Ding · Zhao Shang · Hu Zhao · Renfeng Song · Jianyong Xiong · Chuan He · Dan Liu · Bo Yi

Scientific reports · 2024 doi:10.1038/s41598-024-62370-y

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Experiment

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Data

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Analysis

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title
Anoikis-related gene signatures in colorectal cancer: implications for cell differentiation, immune infiltration, and prognostic prediction.
doi
10.1038/s41598-024-62370-y
pmid
38773226
authors array · 8 items
[0]
Taohui Ding
[1]
Zhao Shang
[2]
Hu Zhao
[3]
Renfeng Song
[4]
Jianyong Xiong
[5]
Chuan He
[6]
Dan Liu
[7]
Bo Yi
journal
Scientific reports
year
2024
abstract
Colorectal cancer (CRC) is a malignant tumor originating from epithelial cells of the colon or rectum, and its invasion and metastasis could be regulated by anoikis. However, the key genes and pathways regulating anoikis in CRC are still unclear and require further research. The single cell transcriptome dataset GSE221575 of GEO database was downloaded and applied to cell subpopulation type identification, intercellular communication, pseudo time cell trajectory analysis, and receptor ligand expression analysis of CRC. Meanwhile, the RNA transcriptome dataset of TCGA, the GSE39582, GSE17536, and GSE17537 datasets of GEO were downloaded and merged into one bulk transcriptome dataset. The differentially expressed genes (DEGs) related to anoikis were extracted from these data sets, and key marker genes were obtained after feature selection. A clinical prognosis prediction model was constructed based on the marker genes and the predictive effect was analyzed. Subsequently, gene pathway analysis, immune infiltration analysis, immunosuppressive point analysis, drug sensitivity analysis, and immunotherapy efficacy based on the key marker genes were conducted for the model. In this study, we used single cell datasets to determine the anoikis activity of cells and analyzed the DEGs of cells based on the score to identify the genes involved in anoikis and extracted DEGs related to the disease from the transcriptome dataset. After dimensionality reduction selection, 7 marker genes were obtained, including TIMP1, VEGFA, MYC, MSLN, EPHA2, ABHD2, and CD24. The prognostic risk model scoring system built by these 7 genes, along with patient clinical data (age, tumor stage, grade), were incorporated to create a nomogram, which predicted the 1-, 3-, and 5-years survival of CRC with accuracy of 0.818, 0.821, and 0.824. By using the scoring system, the CRC samples were divided into high/low anoikis-related prognosis risk groups, there are significant differences in immune infiltration, distribution of immune checkpoints, sensitivity to chemotherapy drugs, and efficacy of immunotherapy between these two risk groups. Anoikis genes participate in the differentiation of colorectal cancer tumor cells, promote tumor development, and could predict the prognosis of colorectal cancer.
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The least absolute shrinkage and selection operator (LASSO) analysis was performed on the prognosis-related genes to further select the characteristic genes and to develop a prognostic model.
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The least absolute shrinkage and selection operator (LASSO) analysis was performed on the prognosis-related genes to further select the characteristic genes and to develop a prognostic model.
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The datasets used in this study are available in TCGA (https://portal.gdc.cancer.gov/), GEO (https://www.ncbi.nlm.nih.gov/geo/), and TIDE databases (http://tide.dfci.harvard.edu/). IMvigor210 database was downloaded by the IMvigor210CoreBiologies R package (http://research-pub.gene.com/IMvigor210CoreBiologies/packageVersions/). The datas generated and analysed during the current study are available from the the article and supplementary information.
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The datasets used in this study are available in TCGA (https://portal.gdc.cancer.gov/), GEO (https://www.ncbi.nlm.nih.gov/geo/), and TIDE databases (http://tide.dfci.harvard.edu/). IMvigor210 database was downloaded by the IMvigor210CoreBiologies R package (http://research-pub.gene.com/IMvigor210CoreBiologies/packageVersions/). The datas generated and analysed during the current study are available from the the article and supplementary information.
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The study identified seven anoikis-related prognostic marker genes and constructed a nomogram with 1-, 3-, and 5-year survival accuracies of 0.818, 0.821, and 0.824, respectively.
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The prognostic risk model scoring system built by these 7 genes, along with patient clinical data (age, tumor stage, grade), were incorporated to create a nomogram, which predicted the 1-, 3-, and 5-years survival of CRC with accuracy of 0.818, 0.821, and 0.824.
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The study identified seven anoikis-related prognostic marker genes and constructed a nomogram with 1-, 3-, and 5-year survival accuracies of 0.818, 0.821, and 0.824, respectively.
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[66]
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[67]
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[68]
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[69]
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[70]
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[71]
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[72]
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[73]
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[74]
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[75]
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[76]
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[77]
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[78]
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[79]
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[80]
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[82]
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[83]
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[84]
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[85]
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[86]
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[87]
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[99]
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[103]
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[104]
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[105]
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[106]
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[113]
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[116]
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[117]
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[118]
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[119]
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[120]
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[123]
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[125]
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[126]
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[127]
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[128]
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[129]
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[130]
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[131]
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[132]
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[133]
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[134]
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[135]
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[136]
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[137]
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[138]
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[139]
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[140]
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[142]
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[143]
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[144]
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[145]
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[146]
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[147]
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[148]
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[149]
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[150]
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[154]
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[155]
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[157]
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[158]
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[159]
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[160]
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[161]
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[162]
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[163]
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[164]
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[165]
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[166]
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[167]
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[168]
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[169]
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[170]
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[171]
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[172]
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[173]
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[174]
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[175]
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[176]
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[177]
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[178]
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[179]
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[180]
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[181]
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[182]
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[183]
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[184]
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[185]
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[186]
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[187]
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[188]
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[189]
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[190]
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[191]
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[192]
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[193]
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[194]
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[195]
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[196]
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[197]
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[198]
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[199]
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[200]
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[201]
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[202]
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[203]
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[204]
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[205]
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[206]
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[207]
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[208]
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[209]
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[210]
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[211]
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[212]
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[213]
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[214]
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[215]
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[216]
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[217]
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[218]
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[219]
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[220]
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[221]
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[222]
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[223]
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[224]
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[225]
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[226]
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[227]
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[228]
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[229]
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[230]
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[231]
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[232]
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[233]
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[234]
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[235]
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[236]
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[237]
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[238]
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[239]
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[240]
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[241]
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[242]
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[243]
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[244]
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[245]
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[246]
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[247]
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[248]
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[249]
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[250]
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[251]
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[252]
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[253]
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[254]
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[255]
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[256]
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[257]
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[258]
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[259]
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[260]
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[261]
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[262]
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[263]
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[264]
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[265]
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[266]
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[267]
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[268]
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[269]
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[270]
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[271]
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[272]
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[273]
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[274]
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[275]
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[276]
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[277]
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[278]
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[279]
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[280]
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[281]
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[282]
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[283]
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[284]
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[285]
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[286]
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[287]
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[288]
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[289]
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[290]
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[291]
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[292]
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[293]
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[294]
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[295]
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[296]
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[297]
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[298]
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[299]
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[300]
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[301]
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[302]
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[303]
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[304]
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[305]
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[306]
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[307]
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[308]
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[309]
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[310]
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[311]
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[312]
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[313]
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[314]
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[315]
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[316]
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[317]
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[318]
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[319]
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[320]
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[321]
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[322]
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[323]
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[324]
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[325]
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[326]
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[327]
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[328]
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[329]
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[330]
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[331]
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[332]
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[333]
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[334]
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[335]
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[336]
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[337]
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[338]
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[339]
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[340]
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[341]
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[342]
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[343]
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[344]
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[345]
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[346]
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[347]
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[348]
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[349]
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[350]
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[351]
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[352]
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[353]
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[354]
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[355]
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[356]
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[357]
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[358]
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[359]
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[360]
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[361]
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[362]
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[363]
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[364]
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[365]
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[366]
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[367]
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[368]
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[369]
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[370]
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[371]
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[372]
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[373]
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[374]
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[375]
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[376]
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[377]
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[378]
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[379]
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[380]
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[381]
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[382]
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[383]
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[384]
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[385]
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[386]
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[387]
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[388]
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[389]
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[390]
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[391]
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[392]
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[393]
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[394]
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[396]
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[397]
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[398]
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[399]
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[400]
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[401]
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[402]
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[403]
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[404]
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[405]
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[406]
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[407]
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[408]
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[409]
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[410]
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[411]
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[412]
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[413]
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[414]
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[415]
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[416]
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[417]
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[418]
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[419]
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[420]
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[421]
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[422]
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[423]
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[424]
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[425]
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[426]
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[427]
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[428]
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[429]
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[430]
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[431]
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[432]
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[433]
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[434]
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[435]
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[436]
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[437]
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[438]
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[439]
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[440]
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[441]
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[442]
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[443]
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[444]
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[445]
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[446]
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[447]
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[448]
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[449]
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[450]
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[451]
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[452]
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[453]
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[454]
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[455]
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[456]
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[457]
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[458]
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[459]
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[460]
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[461]
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[462]
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[463]
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[464]
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[465]
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[466]
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[467]
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[468]
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[469]
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[470]
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[471]
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[472]
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[473]
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[474]
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[475]
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[476]
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[477]
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[479]
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[480]
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[481]
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[482]
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[483]
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[484]
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[485]
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[486]
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[487]
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[488]
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[489]
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[490]
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[491]
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[492]
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[493]
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[494]
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[495]
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[496]
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[497]
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[498]
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[499]
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[500]
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[501]
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[502]
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[503]
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[505]
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[506]
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[512]
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[513]
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[514]
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[515]
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[516]
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[517]
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[518]
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[519]
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[520]
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[521]
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[522]
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[523]
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[524]
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[525]
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[526]
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[527]
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[528]
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[529]
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[530]
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[532]
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[533]
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[534]
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[535]
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[536]
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[537]
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[542]
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[583]
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[584]
GSM972522
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
gaps array · 8 items
[0]
asset:data:geo:GSE17536 not downloaded
[1]
asset:data:geo:GSE17536 licence not read
[2]
asset:data:geo:GSE17537 not downloaded
[3]
asset:data:geo:GSE17537 licence not read
[4]
asset:data:geo:GSE221575 not downloaded
[5]
asset:data:geo:GSE221575 licence not read
[6]
asset:data:geo:GSE39582 not downloaded
[7]
asset:data:geo:GSE39582 licence not read
analysis object · 4 fields
state
partial
methods array · 3 items
[0] object · 10 fields
id
method-1
family
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 · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[1] object · 10 fields
id
method-2
family
network_analysis
specific
pathway_enrichment
label
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
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
quote
GO enrichment
[2] object · 10 fields
id
method-3
family
null
specific
null
label
least absolute shrinkage and selection operator (LASSO) analysis
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
The least absolute shrinkage and selection operator (LASSO) analysis was performed on the prognosis-related genes to further select the characteristic genes and to develop a prognostic model.
targets array · 0 items
gaps array · 2 items
[0]
method.reader_named_unmapped
[1]
method.group_comparison_wilcoxon
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
false
required_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: wilcoxon.
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
R1
reachable
true
accessions array · 4 items
[0]
GSE39582
[1]
GSE17536
[2]
GSE17537
[3]
GSE221575
resolved_accessions array · 4 items
[0]
GSE39582
[1]
GSE17536
[2]
GSE17537
[3]
GSE221575
statements array · 1 item
[0]
The datasets used in this study are available in TCGA (https://portal.gdc.cancer.gov/), GEO (https://www.ncbi.nlm.nih.gov/geo/), and TIDE databases (http://tide.dfci.harvard.edu/). IMvigor210 database was downloaded by the IMvigor210CoreBiologies R package (http://research-pub.gene.com/IMvigor210CoreBiologies/packageVersions/). The datas generated and analysed during the current study are available from the the article and supplementary information.
basis
The paper names GSE39582, GSE17536, GSE17537, GSE221575 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 0 items
assets array · 2 items
[0]
source:pmid:38773226
[1]
data:geo:GSE17536
steps array · 0 items
must_build object · 5 fields
dsl_operations array · 1 item
[0] object · 3 fields
operation
group_comparison_wilcoxon
priority
null
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE17536
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T19:19:05Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
15292
completion_tokens
3217
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38773226", "kind": "science-record", "revision": 4, "content_hash": "sha256:2ccea2e0bbb1f11e5d6d790ea2c0f8c2f335e5a5988bbbd4bb2b15845de56ed4", "created_at": "2026-11-01T19:20:43Z", "updated_at": "2026-11-01T22:11:54Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Anoikis-related gene signatures in colorectal cancer: implications for cell differentiation, immune infiltration, and prognostic prediction.", "doi": "10.1038/s41598-024-62370-y", "pmid": "38773226", "authors": ["Taohui Ding", "Zhao Shang", "Hu Zhao", "Renfeng Song", "Jianyong Xiong", "Chuan He", "Dan Liu", "Bo Yi"], "journal": "Scientific reports", "year": 2024, "abstract": "Colorectal cancer (CRC) is a malignant tumor originating from epithelial cells of the colon or rectum, and its invasion and metastasis could be regulated by anoikis. However, the key genes and pathways regulating anoikis in CRC are still unclear and require further research. The single cell transcriptome dataset GSE221575 of GEO database was downloaded and applied to cell subpopulation type identification, intercellular communication, pseudo time cell trajectory analysis, and receptor ligand expression analysis of CRC. Meanwhile, the RNA transcriptome dataset of TCGA, the GSE39582, GSE17536, and GSE17537 datasets of GEO were downloaded and merged into one bulk transcriptome dataset. The differentially expressed genes (DEGs) related to anoikis were extracted from these data sets, and key marker genes were obtained after feature selection. A clinical prognosis prediction model was constructed based on the marker genes and the predictive effect was analyzed. Subsequently, gene pathway analysis, immune infiltration analysis, immunosuppressive point analysis, drug sensitivity analysis, and immunotherapy efficacy based on the key marker genes were conducted for the model. In this study, we used single cell datasets to determine the anoikis activity of cells and analyzed the DEGs of cells based on the score to identify the genes involved in anoikis and extracted DEGs related to the disease from the transcriptome dataset. After dimensionality reduction selection, 7 marker genes were obtained, including TIMP1, VEGFA, MYC, MSLN, EPHA2, ABHD2, and CD24. The prognostic risk model scoring system built by these 7 genes, along with patient clinical data (age, tumor stage, grade), were incorporated to create a nomogram, which predicted the 1-, 3-, and 5-years survival of CRC with accuracy of 0.818, 0.821, and 0.824. By using the scoring system, the CRC samples were divided into high/low anoikis-related prognosis risk groups, there are significant differences in immune infiltration, distribution of immune checkpoints, sensitivity to chemotherapy drugs, and efficacy of immunotherapy between these two risk groups. Anoikis genes participate in the differentiation of colorectal cancer tumor cells, promote tumor development, and could predict the prognosis of colorectal cancer.", "claims": [{"id": "claim-method", "statement": "The least absolute shrinkage and selection operator (LASSO) analysis was performed on the prognosis-related genes to further select the characteristic genes and to develop a prognostic model.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38773226", "locator": "sections[9] \"Building and validation of a prognosis-prediction model\" paragraph 2", "quote": "The least absolute shrinkage and selection operator (LASSO) analysis was performed on the prognosis-related genes to further select the characteristic genes and to develop a prognostic model."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used in this study are available in TCGA (https://portal.gdc.cancer.gov/), GEO (https://www.ncbi.nlm.nih.gov/geo/), and TIDE databases (http://tide.dfci.harvard.edu/). 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The datas generated and analysed during the current study are available from the the article and supplementary information."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified seven anoikis-related prognostic marker genes and constructed a nomogram with 1-, 3-, and 5-year survival accuracies of 0.818, 0.821, and 0.824, respectively.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38773226", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "The prognostic risk model scoring system built by these 7 genes, along with patient clinical data (age, tumor stage, grade), were incorporated to create a nomogram, which predicted the 1-, 3-, and 5-years survival of CRC with accuracy of 0.818, 0.821, and 0.824."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "The study identified seven anoikis-related prognostic marker genes and constructed a nomogram with 1-, 3-, and 5-year survival accuracies of 0.818, 0.821, and 0.824, respectively.", "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:38773226"], "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. 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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}}], "gaps": ["asset:data:geo:GSE17536 not downloaded", "asset:data:geo:GSE17536 licence not read", "asset:data:geo:GSE17537 not downloaded", "asset:data:geo:GSE17537 licence not read", "asset:data:geo:GSE221575 not downloaded", "asset:data:geo:GSE221575 licence not read", "asset:data:geo:GSE39582 not downloaded", "asset:data:geo:GSE39582 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "group_comparison", "specific": "wilcoxon", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_wilcoxon"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 0.8, "band": 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