ArticleScience progress
Machine learning-driven transcriptomic and single-cell profiling of programed cell death patterns in colon cancer.
Article in Science progress. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
ObjectiveColon cancer ranks among the most prevalent malignancies globally. Despite advances in therapy, patients' prognosis remains poor, particularly in advanced stages. Programed cell death (PCD), including over 20 patterns, plays a pivotal role in colon cancer progression. However, a systematic analysis of the PCD regulatory network in colon cancer is lacking.MethodsWe comprehensively analyzed various PCD patterns in colon cancer using bulk transcriptomic and single-cell transcriptomic data from GEO and TCGA databases. Multiple machine learning algorithms were used to identify Key PCD patterns. A novel combined cell death index (CCDI) was constructed using 117 algorithm combinations. Functional enrichment, immune infiltration, nomogram construction, and pseudotime trajectory analyses were also performed.ResultsDifferent PCD patterns significantly impacted colon cancer prognosis. Disulfidptosis and anoikis were consistently identified as critical PCD patterns. The CCDI, based on these genes, outperformed existing models in prognostic prediction. Additionally, disulfidptosis and anoikis scores enriched in endothelial cells (ECs), which exhibited close interactions with other cell types. Six genes (CD36, CLU, FLNA, NOTCH3, TAGLN, TIMP1) were identified as key regulators during ECs phenotypic transition.ConclusionsThis study demonstrates the key roles of disulfidptosis and anoikis, and establishes a novel CCDI model with prognostic value in colon cancer. Additionally, it insights into ECs phenotypic transition and their regulatory genes, provides new therapy targets for colon cancer.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.