Evidence map›Paper›PMID 31689990›Full record

ArticleCancers2019

Construction and Validation of an Immune-Related Prognostic Model Based on TP53 Status in Colorectal Cancer.

Xiaojuan Zhao, Jianzhong Liu, Shuzhen Liu, Fangfang Yang, Erfei Chen

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Multi-omics landscape and clinical significance of aComputational and structural biotechnology journal · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Identification of a mCancer cell international · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Gene Signatures and Prognostic Values of mFrontiers in oncology · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xiaojuan ZhaoInstitute of Preventive Genomic Medicine, School of Life Sciences, Northwest University, Xi'an 710069, China. xjzhao1992@163.com.
Jianzhong LiuCollege of Environmental and Resource Science, Shanxi University, Taiyuan 030000, China. lliujzzhao@163.com.
Shuzhen LiuInstitute of Preventive Genomic Medicine, School of Life Sciences, Northwest University, Xi'an 710069, China. LSZ15709483140@163.com.
Fangfang YangInstitute of Preventive Genomic Medicine, School of Life Sciences, Northwest University, Xi'an 710069, China. yangff@nwu.edu.cn.
Erfei ChenInstitute of Preventive Genomic Medicine, School of Life Sciences, Northwest University, Xi'an 710069, China. chenerfei@nwu.edu.cn.ORCID 0000-0001-9168-7407

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence has indicated that prognostic biomarkers have a pivotal role in tumor and immunity biological processes. TP53 mutation can cause a range of changes in immune response, progression, and prognosis of colorectal cancer (CRC). Thus, we aim to build an immunoscore prognostic model that may enhance the prognosis of CRC from an immunological perspective. We estimated the proportion of immune cells in the GSE39582 public dataset using the CIBERSORT (Cell type identification by estimating relative subset of known RNA transcripts) algorithm. Prognostic genes that were used to establish the immunoscore model were generated by the LASSO (Least absolute shrinkage and selection operator) Cox regression model. We established and validated the immunoscore model in GEO (Gene Expression Omnibus) and TCGA (The Cancer Genome Atlas) cohorts, respectively; significant differences of overall survival analysis were found between the low and high immunoscore groups or TP53 subgroups. In the multivariable Cox analysis, we observed that the immunoscore was an independent prognostic factor both in the GEO cohort (HR (Hazard ratio) 1.76, 95% CI (confidence intervals): 1.26-2.46) and the TCGA cohort (HR 1.95, 95% CI: 1.20-3.18). Furthermore, we established a nomogram for clinical application, and the results suggest that the nomogram is a better predictive model for prognosis than immunoscore or TNM staging.

Indexed as

CIBERSORTcolorectal cancerimmunoscoreprognosisTP53

Identifiers

PMID31689990
PMCPMC6895875

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.